Name

FGQTL4 Gene

Fasting plasma glucose level QTL 4

FGQTL6 Gene

Fasting plasma glucose level QTL 6

FGQTL1 Gene

Fasting plasma glucose level QTL 1

FGQTL2 Gene

Fasting plasma glucose level QTL2

FGQTL3 Gene

Fasting plasma glucose level QTL3

FIQTL1 Gene

fasting glucose and specific insulin levels

GDPGP1 Gene

GDP-D-glucose phosphorylase 1

LOC100288073 Gene

heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) pseudogene

H6PD Gene

hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)

There are 2 forms of glucose-6-phosphate dehydrogenase. G form is X-linked and H form, encoded by this gene, is autosomally linked. This H form shows activity with other hexose-6-phosphates, especially galactose-6-phosphate, whereas the G form is specific for glucose-6-phosphate. Both forms are present in most tissues, but H form is not found in red cells. [provided by RefSeq, Jul 2008]

SLC37A1 Gene

solute carrier family 37 (glucose-6-phosphate transporter), member 1

SLC37A1, a member of the sugar-phosphate transport family, transports glycerol-3-phosphate (G3P) between cellular compartments for its utilization in several compartment-specific biochemical pathways.[supplied by OMIM, Jul 2004]

UGDH Gene

UDP-glucose 6-dehydrogenase

The protein encoded by this gene converts UDP-glucose to UDP-glucuronate and thereby participates in the biosynthesis of glycosaminoglycans such as hyaluronan, chondroitin sulfate, and heparan sulfate. These glycosylated compounds are common components of the extracellular matrix and likely play roles in signal transduction, cell migration, and cancer growth and metastasis. The expression of this gene is up-regulated by transforming growth factor beta and down-regulated by hypoxia. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

LOC100422548 Gene

solute carrier family 5 (glucose activated ion channel), member 4 pseudogene

LOC100422549 Gene

solute carrier family 5 (glucose activated ion channel), member 4 pseudogene

SLC2AXP1 Gene

solute carrier family 2 (facilitated glucose transporter), pseudogene 1

SOGA1 Gene

suppressor of glucose, autophagy associated 1

G6PC3 Gene

glucose 6 phosphatase, catalytic, 3

This gene encodes the catalytic subunit of glucose-6-phosphatase (G6Pase). G6Pase is located in the endoplasmic reticulum (ER) and catalyzes the hydrolysis of glucose-6-phosphate to glucose and phosphate in the last step of the gluconeogenic and glycogenolytic pathways. Mutations in this gene result in autosomal recessive severe congenital neutropenia. Multiple transcript variants have been found for this gene, only one of which is expected to express a protein.[provided by RefSeq, Sep 2009]

G6PC2 Gene

glucose-6-phosphatase, catalytic, 2

This gene encodes an enzyme belonging to the glucose-6-phosphatase catalytic subunit family. These enzymes are part of a multicomponent integral membrane system that catalyzes the hydrolysis of glucose-6-phosphate, the terminal step in gluconeogenic and glycogenolytic pathways, allowing the release of glucose into the bloodstream. The family member encoded by this gene is found in pancreatic islets and does not exhibit phosphohydrolase activity, but it is a major target of cell-mediated autoimmunity in diabetes. Several alternatively spliced transcript variants of this gene have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]

UGGT2 Gene

UDP-glucose glycoprotein glucosyltransferase 2

UDP-glucose:glycoprotein glucosyltransferase (UGT) is a soluble protein of the endoplasmic reticulum (ER) that selectively reglucosylates unfolded glycoproteins, thus providing quality control for protein transport out of the ER.[supplied by OMIM, Oct 2009]

UGGT1 Gene

UDP-glucose glycoprotein glucosyltransferase 1

UDP-glucose:glycoprotein glucosyltransferase (UGT) is a soluble protein of the endoplasmic reticulum (ER) that selectively reglucosylates unfolded glycoproteins, thus providing quality control for protein transport out of the ER.[supplied by OMIM, Oct 2009]

SLC2A10 Gene

solute carrier family 2 (facilitated glucose transporter), member 10

This gene encodes a member of the class III facilitative glucose transporter family. The encoded protein plays a role in regulation of glucose homeostasis. Mutations in this gene have been associated with arterial tortuosity syndrome.[provided by RefSeq, Dec 2009]

UGCG Gene

UDP-glucose ceramide glucosyltransferase

This gene encodes an enzyme that catalyzes the first glycosylation step in the biosynthesis of glycosphingolipids, which are membrane components containing lipid and sugar moieties. The product of this reaction is glucosylceramide, which is the core structure of many glycosphingolipids. [provided by RefSeq, Dec 2014]

SLC37A2 Gene

solute carrier family 37 (glucose-6-phosphate transporter), member 2

SLC37A4 Gene

solute carrier family 37 (glucose-6-phosphate transporter), member 4

This gene regulates glucose-6-phosphate transport from the cytoplasm to the lumen of the endoplasmic reticulum, in order to maintain glucose homeostasis. It also plays a role in ATP-mediated calcium sequestration in the lumen of the endoplasmic reticulum. Mutations in this gene have been associated with various forms of glycogen storage disease. Alternative splicing in this gene results in multiple transcript variants.[provided by RefSeq, Aug 2009]

LOC105379282 Gene

glucose-dependent insulinotropic receptor-like

G6PD Gene

glucose-6-phosphate dehydrogenase

This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

G6PC Gene

glucose-6-phosphatase, catalytic subunit

Glucose-6-phosphatase (G6Pase) is a multi-subunit integral membrane protein of the endoplasmic reticulum that is composed of a catalytic subunit and transporters for G6P, inorganic phosphate, and glucose. This gene (G6PC) is one of the three glucose-6-phosphatase catalytic-subunit-encoding genes in human: G6PC, G6PC2 and G6PC3. Glucose-6-phosphatase catalyzes the hydrolysis of D-glucose 6-phosphate to D-glucose and orthophosphate and is a key enzyme in glucose homeostasis, functioning in gluconeogenesis and glycogenolysis. Mutations in this gene cause glycogen storage disease type I (GSD1). This disease, also known as von Gierke disease, is a metabolic disorder characterized by severe hypoglycemia associated with the accumulation of glycogen and fat in the liver and kidneys.[provided by RefSeq, Feb 2011]

G6PR Gene

glucose-6-phosphatase regulator

GPI Gene

glucose-6-phosphate isomerase

This gene encodes a member of the glucose phosphate isomerase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. In the cytoplasm, the gene product functions as a glycolytic enzyme (glucose-6-phosphate isomerase) that interconverts glucose-6-phophsate and fructose-6-phosphate. Extracellularly, the encoded protein (also referred to as neuroleukin) functions as a neurotrophic factor that promotes survival of skeletal motor neurons and sensory neurons, and as a lymphokine that induces immunoglobulin secretion. The encoded protein is also referred to as autocrine motility factor based on an additional function as a tumor-secreted cytokine and angiogenic factor. Defects in this gene are the cause of nonspherocytic hemolytic anemia and a severe enzyme deficiency can be associated with hydrops fetalis, immediate neonatal death and neurological impairment. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2014]

SLC2A14 Gene

solute carrier family 2 (facilitated glucose transporter), member 14

Members of the glucose transporter (GLUT) family, including SLC2A14, are highly conserved integral membrane proteins that transport hexoses such as glucose and fructose into all mammalian cells. GLUTs show tissue and cell-type specific expression (Wu and Freeze, 2002 [PubMed 12504846]).[supplied by OMIM, Mar 2008]

SLC2A13 Gene

solute carrier family 2 (facilitated glucose transporter), member 13

SLC2A12 Gene

solute carrier family 2 (facilitated glucose transporter), member 12

SLC2A12 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion (Rogers et al., 2002). This family of transporters show conservation of 12 transmembrane helices as well as functionally significant amino acid residues (Joost and Thorens, 2001 [PubMed 11780753]).[supplied by OMIM, Mar 2008]

SLC2A11 Gene

solute carrier family 2 (facilitated glucose transporter), member 11

This gene belongs to a family of proteins that mediate the transport of sugars across the cell membrane. The encoded protein transports glucose and fructose. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]

GFOD2 Gene

glucose-fructose oxidoreductase domain containing 2

GFOD1 Gene

glucose-fructose oxidoreductase domain containing 1

UGP2 Gene

UDP-glucose pyrophosphorylase 2

The enzyme encoded by this gene is an important intermediary in mammalian carbohydrate interconversions. It transfers a glucose moiety from glucose-1-phosphate to MgUTP and forms UDP-glucose and MgPPi. In liver and muscle tissue, UDP-glucose is a direct precursor of glycogen; in lactating mammary gland it is converted to UDP-galactose which is then converted to lactose. The eukaryotic enzyme has no significant sequence similarity to the prokaryotic enzyme. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

SLC5A1 Gene

solute carrier family 5 (sodium/glucose cotransporter), member 1

This gene encodes a member of the sodium-dependent glucose transporter (SGLT) family. The encoded integral membrane protein is the primary mediator of dietary glucose and galactose uptake from the intestinal lumen. Mutations in this gene have been associated with glucose-galactose malabsorption. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]

SLC5A2 Gene

solute carrier family 5 (sodium/glucose cotransporter), member 2

This gene encodes a member of the sodium glucose cotransporter family which are sodium-dependent glucose transport proteins. The encoded protein is the major cotransporter involved in glucose reabsorption in the kidney. Mutations in this gene are associated with renal glucosuria. Two transcript variants, one protein-coding and one not, have been found for this gene. [provided by RefSeq, Feb 2015]

SLC5A4 Gene

solute carrier family 5 (glucose activated ion channel), member 4

SLC35D2 Gene

solute carrier family 35 (UDP-GlcNAc/UDP-glucose transporter), member D2

Nucleotide sugars, which are synthesized in the cytosol or the nucleus, are high-energy donor substrates for glycosyltransferases located in the lumen of the endoplasmic reticulum and Golgi apparatus. Translocation of nucleotide sugars from the cytosol into the lumen compartment is mediated by specific nucleotide sugar transporters, such as SLC35D2 (Suda et al., 2004 [PubMed 15082721]).[supplied by OMIM, Mar 2008]

LOC100421868 Gene

glucose-fructose oxidoreductase domain containing 2 pseudogene

SLC5A4P1 Gene

solute carrier family 5 (glucose activated ion channel), member 4 pseudogene 1

HSPA5 Gene

heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)

The protein encoded by this gene is a member of the heat shock protein 70 (HSP70) family. It is localized in the lumen of the endoplasmic reticulum (ER), and is involved in the folding and assembly of proteins in the ER. As this protein interacts with many ER proteins, it may play a key role in monitoring protein transport through the cell.[provided by RefSeq, Sep 2010]

SLC2A3P2 Gene

solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 2

SLC2A3P1 Gene

solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 1

SLC2A3P4 Gene

solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 4

LOC400750 Gene

heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa) pseudogene

SLC2A9 Gene

solute carrier family 2 (facilitated glucose transporter), member 9

This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cartilage matrices. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

SLC2A8 Gene

solute carrier family 2 (facilitated glucose transporter), member 8

This gene belongs to the solute carrier 2A family, which includes intracellular glucose transporters. Based on sequence comparison, the glucose transporters are grouped into three classes and this gene is a member of class II. The encoded protein, like other members of the family, contains several conserved residues and motifs and 12 transmembrane domains with both amino and carboxyl ends being on the cytosolic side of the membrane. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, Nov 2012]

SLC2A7 Gene

solute carrier family 2 (facilitated glucose transporter), member 7

SLC2A7 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion (Li et al., 2004). This family of transporters shows conservation of 12 transmembrane helices as well as functionally significant amino acid residues (Joost and Thorens, 2001 [PubMed 11780753]).[supplied by OMIM, Mar 2008]

SLC2A6 Gene

solute carrier family 2 (facilitated glucose transporter), member 6

Hexose transport into mammalian cells is catalyzed by a family of membrane proteins, including SLC2A6, that contain 12 transmembrane domains and a number of critical conserved residues.[supplied by OMIM, Jul 2002]

SLC2A5 Gene

solute carrier family 2 (facilitated glucose/fructose transporter), member 5

SLC2A4 Gene

solute carrier family 2 (facilitated glucose transporter), member 4

This gene is a member of the solute carrier family 2 (facilitated glucose transporter) family and encodes a protein that functions as an insulin-regulated facilitative glucose transporter. In the absence of insulin, this integral membrane protein is sequestered within the cells of muscle and adipose tissue. Within minutes of insulin stimulation, the protein moves to the cell surface and begins to transport glucose across the cell membrane. Mutations in this gene have been associated with noninsulin-dependent diabetes mellitus (NIDDM). [provided by RefSeq, Jul 2008]

SLC2A3 Gene

solute carrier family 2 (facilitated glucose transporter), member 3

SLC2A2 Gene

solute carrier family 2 (facilitated glucose transporter), member 2

This gene encodes an integral plasma membrane glycoprotein of the liver, islet beta cells, intestine, and kidney epithelium. The encoded protein mediates facilitated bidirectional glucose transport. Because of its low affinity for glucose, it has been suggested as a glucose sensor. Mutations in this gene are associated with susceptibility to diseases, including Fanconi-Bickel syndrome and noninsulin-dependent diabetes mellitus (NIDDM). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]

SLC2A1 Gene

solute carrier family 2 (facilitated glucose transporter), member 1

This gene encodes a major glucose transporter in the mammalian blood-brain barrier. The encoded protein is found primarily in the cell membrane and on the cell surface, where it can also function as a receptor for human T-cell leukemia virus (HTLV) I and II. Mutations in this gene have been found in a family with paroxysmal exertion-induced dyskinesia. [provided by RefSeq, Apr 2013]

TGDS Gene

TDP-glucose 4,6-dehydratase

The protein encoded by this gene is a member of the short-chain dehydrogenases/reductases (SDR) superfamily, and is thought to contain a nicotinamide adenine dinucleotide (NAD) binding domain. This large SDR family of enzymes is involved in the metabolism of a variety of compounds, including prostaglandins, retinoids, lipids, steroid hormones, and xenobiotics. Mutations in this gene have been associated with Catel-Manzke syndrome, which is characterized by Pierre Robin sequence, and radial deviation of the index finger due to the presence of an accessory bone between the index finger and its proximal phalanx. Pierre Robin sequence is defined by an undersized jaw, backwards displacement of the tongue base that causes an obstruction of the airways, and can also be associated with a cleft palate. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]

ART4 Gene

ADP-ribosyltransferase 4 (Dombrock blood group)

This gene encodes a protein that contains a mono-ADP-ribosylation (ART) motif. It is a member of the ADP-ribosyltransferase gene family but enzymatic activity has not been demonstrated experimentally. Antigens of the Dombrock blood group system are located on the gene product, which is glycosylphosphatidylinosotol-anchored to the erythrocyte membrane. Allelic variants, some of which lead to adverse transfusion reactions, are known. [provided by RefSeq, Jul 2008]

GCNT2 Gene

glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group)

This gene encodes the enzyme responsible for formation of the blood group I antigen. The i and I antigens are distinguished by linear and branched poly-N-acetyllactosaminoglycans, respectively. The encoded protein is the I-branching enzyme, a beta-1,6-N-acetylglucosaminyltransferase responsible for the conversion of fetal i antigen to adult I antigen in erythrocytes during embryonic development. Mutations in this gene have been associated with adult i blood group phenotype. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]

LOC100422225 Gene

ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) pseudogene

BP49 Gene

Blood pressure QTL 49

C4B Gene

complement component 4B (Chido blood group)

This gene encodes the basic form of complement factor 4, part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. In addition, this gene exists as a long form and a short form due to the presence or absence of a 6.4 kb endogenous HERV-K retrovirus in intron 9. [provided by RefSeq, Jul 2008]

BP24 Gene

Blood pressure QTL 24

BP25 Gene

Blood pressure QTL 25

BP26 Gene

Blood pressure QTL 26

BP27 Gene

Blood pressure QTL 27

BP20 Gene

Blood pressure QTL 20

BP21 Gene

Blood pressure QTL 21

BP22 Gene

Blood pressure QTL 22

BP23 Gene

Blood pressure QTL 23

BP28 Gene

Blood pressure QTL 28

BP29 Gene

Blood pressure QTL 29

SF Gene

Stoltzfus blood group

SLC4A1 Gene

solute carrier family 4 (anion exchanger), member 1 (Diego blood group)

The protein encoded by this gene is part of the anion exchanger (AE) family and is expressed in the erythrocyte plasma membrane, where it functions as a chloride/bicarbonate exchanger involved in carbon dioxide transport from tissues to lungs. The protein comprises two domains that are structurally and functionally distinct. The N-terminal 40kDa domain is located in the cytoplasm and acts as an attachment site for the red cell skeleton by binding ankyrin. The glycosylated C-terminal membrane-associated domain contains 12-14 membrane spanning segments and carries out the stilbene disulphonate-sensitive exchange transport of anions. The cytoplasmic tail at the extreme C-terminus of the membrane domain binds carbonic anhydrase II. The encoded protein associates with the red cell membrane protein glycophorin A and this association promotes the correct folding and translocation of the exchanger. This protein is predominantly dimeric but forms tetramers in the presence of ankyrin. Many mutations in this gene are known in man, and these mutations can lead to two types of disease: destabilization of red cell membrane leading to hereditary spherocytosis, and defective kidney acid secretion leading to distal renal tubular acidosis. Other mutations that do not give rise to disease result in novel blood group antigens, which form the Diego blood group system. Southeast Asian ovalocytosis (SAO, Melanesian ovalocytosis) results from the heterozygous presence of a deletion in the encoded protein and is common in areas where Plasmodium falciparum malaria is endemic. One null mutation in this gene is known, resulting in very severe anemia and nephrocalcinosis. [provided by RefSeq, Jul 2008]

ABCB6 Gene

ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This half-transporter likely plays a role in mitochondrial function. Localized to 2q26, this gene is considered a candidate gene for lethal neonatal metabolic syndrome, a disorder of mitochondrial function. [provided by RefSeq, Jul 2008]

XK Gene

X-linked Kx blood group

This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008]

XG Gene

Xg blood group

This gene encodes the XG blood group antigen, and is located at the pseudoautosomal boundary on the short (p) arm of chromosome X. The three 5' exons reside in the pseudoautosomal region and the remaining exons within the X-specific end. A truncated copy of this gene is found on the Y chromosome at the pseudoautosomal boundary. It is transcribed, but not expected to make a Y-chromosome specific gene product. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2008]

CD55 Gene

CD55 molecule, decay accelerating factor for complement (Cromer blood group)

This gene encodes a glycoprotein involved in the regulation of the complement cascade. Binding of the encoded protein to complement proteins accelerates their decay, thereby disrupting the cascade and preventing damage to host cells. Antigens present on this protein constitute the Cromer blood group system (CROM). Alternative splicing results in multiple transcript variants. The predominant transcript variant encodes a membrane-bound protein, but alternatively spliced transcripts may produce soluble proteins. [provided by RefSeq, Jul 2014]

LOC100422194 Gene

ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) pseudogene

ERMAP Gene

erythroblast membrane-associated protein (Scianna blood group)

The protein encoded by this gene is a cell surface transmembrane protein that may act as an erythroid cell receptor, possibly as a mediator of cell adhesion. Polymorphisms in this gene are responsible for the Scianna/Radin blood group system. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

BP1 Gene

Blood pressure QTL 1

BP3 Gene

Blood pressure QTL 3

BP2 Gene

Blood pressure QTL 2

BP5 Gene

Blood pressure QTL 5

BP4 Gene

Blood pressure QTL 4

BP7 Gene

Blood pressure QTL 7

BP6 Gene

Blood pressure QTL 6

BP9 Gene

Blood pressure QTL 9

BP8 Gene

Blood pressure QTL 8

AQP3 Gene

aquaporin 3 (Gill blood group)

This gene encodes the water channel protein aquaporin 3. Aquaporins are a family of small integral membrane proteins related to the major intrinsic protein, also known as aquaporin 0. Aquaporin 3 is localized at the basal lateral membranes of collecting duct cells in the kidney. In addition to its water channel function, aquaporin 3 has been found to facilitate the transport of nonionic small solutes such as urea and glycerol, but to a smaller degree. It has been suggested that water channels can be functionally heterogeneous and possess water and solute permeation mechanisms. [provided by RefSeq, Aug 2011]

LOC401913 Gene

ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase) pseudogene

SLC14A1 Gene

solute carrier family 14 (urea transporter), member 1 (Kidd blood group)

The protein encoded by this gene is a membrane transporter that mediates urea transport in erythrocytes. This gene forms the basis for the Kidd blood group system. [provided by RefSeq, Mar 2009]

ABCG2 Gene

ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group)

The membrane-associated protein encoded by this gene is included in the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. Alternatively referred to as a breast cancer resistance protein, this protein functions as a xenobiotic transporter which may play a major role in multi-drug resistance. It likely serves as a cellular defense mechanism in response to mitoxantrone and anthracycline exposure. Significant expression of this protein has been observed in the placenta, which may suggest a potential role for this molecule in placenta tissue. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]

KEL Gene

Kell blood group, metallo-endopeptidase

This gene encodes a type II transmembrane glycoprotein that is the highly polymorphic Kell blood group antigen. The Kell glycoprotein links via a single disulfide bond to the XK membrane protein that carries the Kx antigen. The encoded protein contains sequence and structural similarity to members of the neprilysin (M13) family of zinc endopeptidases. [provided by RefSeq, Jul 2008]

LOC100499223 Gene

beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) pseudogene

ACKR1 Gene

atypical chemokine receptor 1 (Duffy blood group)

The protein encoded by this gene is a glycosylated membrane protein and a non-specific receptor for several chemokines. The encoded protein is the receptor for the human malarial parasites Plasmodium vivax and Plasmodium knowlesi. Polymorphisms in this gene are the basis of the Duffy blood group system. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

SEMA7A Gene

semaphorin 7A, GPI membrane anchor (John Milton Hagen blood group)

The protein encoded by this gene binds to cell surfaces through a glycosylphosphatidylinositol (GPI) linkage. The encoded glycoprotein is found on activated lymphocytes and erythrocytes. This protein may be involved in immunomodulatory and neuronal processes. Defects in this gene can result in loss of bone mineral density (BMD). Three transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Mar 2009]

XKRYP6 Gene

XK, Kell blood group complex subunit-related, Y-linked pseudogene 6

XKRYP4 Gene

XK, Kell blood group complex subunit-related, Y-linked pseudogene 4

XKRYP5 Gene

XK, Kell blood group complex subunit-related, Y-linked pseudogene 5

XKRYP2 Gene

XK, Kell blood group complex subunit-related, Y-linked pseudogene 2

XKRYP3 Gene

XK, Kell blood group complex subunit-related, Y-linked pseudogene 3

XKRYP1 Gene

XK, Kell blood group complex subunit-related, Y-linked pseudogene 1

FUT3 Gene

fucosyltransferase 3 (galactoside 3(4)-L-fucosyltransferase, Lewis blood group)

The Lewis histo-blood group system comprises a set of fucosylated glycosphingolipids that are synthesized by exocrine epithelial cells and circulate in body fluids. The glycosphingolipids function in embryogenesis, tissue differentiation, tumor metastasis, inflammation, and bacterial adhesion. They are secondarily absorbed to red blood cells giving rise to their Lewis phenotype. This gene is a member of the fucosyltransferase family, which catalyzes the addition of fucose to precursor polysaccharides in the last step of Lewis antigen biosynthesis. It encodes an enzyme with alpha(1,3)-fucosyltransferase and alpha(1,4)-fucosyltransferase activities. Mutations in this gene are responsible for the majority of Lewis antigen-negative phenotypes. Multiple alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]

FUT1 Gene

fucosyltransferase 1 (galactoside 2-alpha-L-fucosyltransferase, H blood group)

The protein encoded by this gene is a Golgi stack membrane protein that is involved in the creation of a precursor of the H antigen, which is required for the final step in the soluble A and B antigen synthesis pathway. This gene is one of two encoding the galactoside 2-L-fucosyltransferase enzyme. Mutations in this gene are a cause of the H-Bombay blood group. [provided by RefSeq, Jul 2008]

AQP1 Gene

aquaporin 1 (Colton blood group)

Aquaporins are a family of small integral membrane proteins related to the major intrinsic protein (MIP or AQP0). This gene encodes an aquaporin which functions as a molecular water channel protein. It is a homotetramer with 6 bilayer spanning domains and N-glycosylation sites. The protein physically resembles channel proteins and is abundant in erythrocytes and renal tubes. The gene encoding this aquaporin is a possible candidate for disorders involving imbalance in ocular fluid movement. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]

SMIM1 Gene

small integral membrane protein 1 (Vel blood group)

This gene encodes a small, conserved protein that participates in red blood cell formation. The encoded protein is localized to the cell membrane and is the antigen for the Vel blood group. Alternative splicing results in different transcript variants that encode the same protein. [provided by RefSeq, Dec 2013]

LOC100533842 Gene

ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group) pseudogene

ICAM4 Gene

intercellular adhesion molecule 4 (Landsteiner-Wiener blood group)

This gene encodes the Landsteiner-Wiener (LW) blood group antigen(s) that belongs to the immunoglobulin (Ig) superfamily, and that shares similarity with the intercellular adhesion molecule (ICAM) protein family. This ICAM protein contains 2 Ig-like C2-type domains and binds to the leukocyte adhesion LFA-1 protein. The molecular basis of the LW(A)/LW(B) blood group antigens is a single aa variation at position 100; Gln-100=LW(A) and Arg-100=LW(B). Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]

BP51 Gene

Blood pressure QTL 51

BP50 Gene

Blood pressure QTL 50

BP53 Gene

Blood pressure QTL 53

BP52 Gene

Blood pressure QTL 52

BP55 Gene

Blood pressure QTL 55

BP54 Gene

Blood pressure QTL 54

PFBI Gene

Plasmodium falciparum blood infection levels

RHD Gene

Rh blood group, D antigen

The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene, which encodes the RhD protein, and a second gene that encodes both the RhC and RhE antigens on a single polypeptide. The two genes, and a third unrelated gene, are found in a cluster on chromosome 1. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

CR1 Gene

complement component (3b/4b) receptor 1 (Knops blood group)

This gene is a member of the receptors of complement activation (RCA) family and is located in the 'cluster RCA' region of chromosome 1. The gene encodes a monomeric single-pass type I membrane glycoprotein found on erythrocytes, leukocytes, glomerular podocytes, and splenic follicular dendritic cells. The Knops blood group system is a system of antigens located on this protein. The protein mediates cellular binding to particles and immune complexes that have activated complement. Decreases in expression of this protein and/or mutations in its gene have been associated with gallbladder carcinomas, mesangiocapillary glomerulonephritis, systemic lupus erythematosus and sarcoidosis. Mutations in this gene have also been associated with a reduction in Plasmodium falciparum rosetting, conferring protection against severe malaria. Alternate allele-specific splice variants, encoding different isoforms, have been characterized. Additional allele specific isoforms, including a secreted form, have been described but have not been fully characterized. [provided by RefSeq, Jul 2008]

CD151 Gene

CD151 molecule (Raph blood group)

The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility. This encoded protein is a cell surface glycoprotein that is known to complex with integrins and other transmembrane 4 superfamily proteins. It is involved in cellular processes including cell adhesion and may regulate integrin trafficking and/or function. This protein enhances cell motility, invasion and metastasis of cancer cells. Multiple alternatively spliced transcript variants that encode the same protein have been described for this gene. [provided by RefSeq, Jul 2008]

B3GALNT1 Gene

beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group)

This gene is a member of the beta-1,3-galactosyltransferase (beta3GalT) gene family. This family encodes type II membrane-bound glycoproteins with diverse enzymatic functions using different donor substrates (UDP-galactose and UDP-N-acetylglucosamine) and different acceptor sugars (N-acetylglucosamine, galactose, N-acetylgalactosamine). The beta3GalT genes are distantly related to the Drosophila Brainiac gene and have the protein coding sequence contained in a single exon. The beta3GalT proteins also contain conserved sequences not found in the beta4GalT or alpha3GalT proteins. The carbohydrate chains synthesized by these enzymes are designated as type 1, whereas beta4GalT enzymes synthesize type 2 carbohydrate chains. The ratio of type 1:type 2 chains changes during embryogenesis. By sequence similarity, the beta3GalT genes fall into at least two groups: beta3GalT4 and 4 other beta3GalT genes (beta3GalT1-3, beta3GalT5). The encoded protein of this gene does not use N-acetylglucosamine as an acceptor sugar at all. Multiple transcript variants that are alternatively spliced in the 5' UTR have been described; they all encode the same protein. [provided by RefSeq, Jul 2008]

BSG Gene

basigin (Ok blood group)

The protein encoded by this gene is a plasma membrane protein that is important in spermatogenesis, embryo implantation, neural network formation, and tumor progression. The encoded protein is also a member of the immunoglobulin superfamily. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

SEC1P Gene

secretory blood group 1, pseudogene

GYPA Gene

glycophorin A (MNS blood group)

Glycophorins A (GYPA) and B (GYPB) are major sialoglycoproteins of the human erythrocyte membrane which bear the antigenic determinants for the MN and Ss blood groups. In addition to the M or N and S or s antigens that commonly occur in all populations, about 40 related variant phenotypes have been identified. These variants include all the variants of the Miltenberger complex and several isoforms of Sta, as well as Dantu, Sat, He, Mg, and deletion variants Ena, S-s-U- and Mk. Most of the variants are the result of gene recombinations between GYPA and GYPB. [provided by RefSeq, Jul 2008]

GYPB Gene

glycophorin B (MNS blood group)

Glycophorins A (GYPA) and B (GYPB) are major sialoglycoproteins of the human erythrocyte membrane which bear the antigenic determinants for the MN and Ss blood groups. GYPB gene consists of 5 exons and has 97% sequence homology with GYPA from the 5' UTR to the coding sequence encoding the first 45 amino acids. In addition to the M or N and S or s antigens, that commonly occur in all populations, about 40 related variant phenotypes have been identified. These variants include all the variants of the Miltenberger complex and several isoforms of Sta; also, Dantu, Sat, He, Mg, and deletion variants Ena, S-s-U- and Mk. Most of the variants are the result of gene recombinations between GYPA and GYPB. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2015]

GYPC Gene

glycophorin C (Gerbich blood group)

Glycophorin C (GYPC) is an integral membrane glycoprotein. It is a minor species carried by human erythrocytes, but plays an important role in regulating the mechanical stability of red cells. A number of glycophorin C mutations have been described. The Gerbich and Yus phenotypes are due to deletion of exon 3 and 2, respectively. The Webb and Duch antigens, also known as glycophorin D, result from single point mutations of the glycophorin C gene. The glycophorin C protein has very little homology with glycophorins A and B. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2012]

GYPE Gene

glycophorin E (MNS blood group)

The protein encoded by this gene is a sialoglycoprotein and a type I membrane protein. It is a member of a gene family with GPA and GPB genes. This encoded protein might carry the M blood group antigen. GYPA, GYPB, and GYPE are organized in tandem on chromosome 4. This gene might have derived from an ancestral gene common to the GPB gene by gene duplication. Two alternatively spliced transcript variants encoding the same protein have been described for this gene. [provided by RefSeq, Jul 2008]

XKR9 Gene

XK, Kell blood group complex subunit-related family, member 9

XKR8 Gene

XK, Kell blood group complex subunit-related family, member 8

LOC100422434 Gene

complement component (3b/4b) receptor 1 (Knops blood group) pseudogene

C4B_2 Gene

complement component 4B (Chido blood group), copy 2

This gene encodes the basic form of complement factor 4, part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain may be cleaved to release C4 anaphylatoxin, a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. In addition, this gene exists as a long form and a short form due to the presence or absence of a 6.4 kb endogenous HERV-K retrovirus in intron 9. This GeneID and its associated RefSeq record represent a second copy of C4B found on ALT_REF_LOCI_7. [provided by RefSeq, Jul 2011]

C4A Gene

complement component 4A (Rodgers blood group)

This gene encodes the acidic form of complement factor 4, part of the classical activation pathway. The protein is expressed as a single chain precursor which is proteolytically cleaved into a trimer of alpha, beta, and gamma chains prior to secretion. The trimer provides a surface for interaction between the antigen-antibody complex and other complement components. The alpha chain is cleaved to release C4 anaphylatoxin, an antimicrobial peptide and a mediator of local inflammation. Deficiency of this protein is associated with systemic lupus erythematosus and type I diabetes mellitus. This gene localizes to the major histocompatibility complex (MHC) class III region on chromosome 6. Varying haplotypes of this gene cluster exist, such that individuals may have 1, 2, or 3 copies of this gene. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Nov 2014]

BP37 Gene

Blood pressure QTL 37

BP36 Gene

Blood pressure QTL 36

BP35 Gene

Blood pressure QTL 35

BP34 Gene

Blood pressure QTL 34

BP33 Gene

Blood pressure QTL 33

BP32 Gene

Blood pressure QTL 32

BP31 Gene

Blood pressure QTL 31

BP30 Gene

Blood pressure QTL 30

BP39 Gene

Blood pressure QTL 39

BP38 Gene

Blood pressure QTL 38

BVES Gene

blood vessel epicardial substance

This gene encodes a member of the POP family of proteins containing three putative transmembrane domains. This gene is expressed in cardiac and skeletal muscle and may play an important role in development of these tissues. The mouse ortholog may be involved in the regeneration of adult skeletal muscle and may act as a cell adhesion molecule in coronary vasculogenesis. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Dec 2010]

BP18 Gene

Blood pressure QTL 18

BP14 Gene

Blood pressure QTL 14

XKRY2 Gene

XK, Kell blood group complex subunit-related, Y-linked 2

This gene is located in the nonrecombining portion of the Y chromosome, and is expressed specifically in testis. It encodes a protein which is similar to XK (X-linked Kell blood group precursor), a putative membrane transport protein. This gene is present as two identical copies within a palindromic region; this record represents the more telomeric copy. [provided by RefSeq, Jul 2008]

ACHE Gene

acetylcholinesterase (Yt blood group)

Acetylcholinesterase hydrolyzes the neurotransmitter, acetylcholine at neuromuscular junctions and brain cholinergic synapses, and thus terminates signal transmission. It is also found on the red blood cell membranes, where it constitutes the Yt blood group antigen. Acetylcholinesterase exists in multiple molecular forms which possess similar catalytic properties, but differ in their oligomeric assembly and mode of cell attachment to the cell surface. It is encoded by the single ACHE gene, and the structural diversity in the gene products arises from alternative mRNA splicing, and post-translational associations of catalytic and structural subunits. The major form of acetylcholinesterase found in brain, muscle and other tissues is the hydrophilic species, which forms disulfide-linked oligomers with collagenous, or lipid-containing structural subunits. The other, alternatively spliced form, expressed primarily in the erythroid tissues, differs at the C-terminal end, and contains a cleavable hydrophobic peptide with a GPI-anchor site. It associates with the membranes through the phosphoinositide (PI) moieties added post-translationally. [provided by RefSeq, Jul 2008]

CD44 Gene

CD44 molecule (Indian blood group)

The protein encoded by this gene is a cell-surface glycoprotein involved in cell-cell interactions, cell adhesion and migration. It is a receptor for hyaluronic acid (HA) and can also interact with other ligands, such as osteopontin, collagens, and matrix metalloproteinases (MMPs). This protein participates in a wide variety of cellular functions including lymphocyte activation, recirculation and homing, hematopoiesis, and tumor metastasis. Transcripts for this gene undergo complex alternative splicing that results in many functionally distinct isoforms, however, the full length nature of some of these variants has not been determined. Alternative splicing is the basis for the structural and functional diversity of this protein, and may be related to tumor metastasis. [provided by RefSeq, Jul 2008]

BP46 Gene

Blood pressure QTL 46

BP47 Gene

Blood pressure QTL 47

BP45 Gene

Blood pressure QTL 45

BP48 Gene

Blood pressure QTL 48

AN Gene

blood group Ahonen

ABO Gene

ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)

This gene encodes proteins related to the first discovered blood group system, ABO. Which allele is present in an individual determines the blood group. The 'O' blood group is caused by a deletion of guanine-258 near the N-terminus of the protein which results in a frameshift and translation of an almost entirely different protein. Individuals with the A, B, and AB alleles express glycosyltransferase activities that convert the H antigen into the A or B antigen. Other minor alleles have been found for this gene. [provided by RefSeq, Jul 2008]

XKRY Gene

XK, Kell blood group complex subunit-related, Y-linked

This gene is located in the nonrecombining portion of the Y chromosome, and is expressed specifically in testis. It encodes a protein which is similar to XK (X-linked Kell blood group precursor), a putative membrane transport protein. This gene is present as two identical copies within a palindromic region; this record represents the more centromeric copy. [provided by RefSeq, Jul 2008]

XKRX Gene

XK, Kell blood group complex subunit-related, X-linked

This gene encodes a protein that is related to a component of the XK/Kell complex of the Kell blood group system. The encoded protein includes several transmembrane domains, is known to be exposed to the cell surface, and may function as a membrane transporter. [provided by RefSeq, May 2010]

XKR5 Gene

XK, Kell blood group complex subunit-related family, member 5

XKR4 Gene

XK, Kell blood group complex subunit-related family, member 4

XKR7 Gene

XK, Kell blood group complex subunit-related family, member 7

XKR6 Gene

XK, Kell blood group complex subunit-related family, member 6

XKR3 Gene

XK, Kell blood group complex subunit-related family, member 3

XKRX (MIM 300684) and XKR3 are homologs of the Kell blood group precursor XK (MIM 314850), which is a putative membrane transporter and a component of the XK/Kell complex of the Kell blood group system (Calenda et al., 2006 [PubMed 16431037]).[supplied by OMIM, Mar 2008]

LOC100422564 Gene

glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group) pseudogene

BP19 Gene

Blood pressure QTL 19

BP15 Gene

Blood pressure QTL 15

BP17 Gene

Blood pressure QTL 17

BP16 Gene

Blood pressure QTL 16

BP11 Gene

Blood pressure QTL 11

BP10 Gene

Blood pressure QTL 10

BP13 Gene

Blood pressure QTL 13

BP12 Gene

Blood pressure QTL 12

BCAM Gene

basal cell adhesion molecule (Lutheran blood group)

This gene encodes Lutheran blood group glycoprotein, a member of the immunoglobulin superfamily and a receptor for the extracellular matrix protein, laminin. The protein contains five extracellular immunoglobulin domains, a single transmembrane domain, and a short C-terminal cytoplasmic tail. This protein may play a role in epithelial cell cancer and in vaso-occlusion of red blood cells in sickle cell disease. Polymorphisms in this gene define some of the antigens in the Lutheran system and also the Auberger system. Inactivating variants of this gene result in the recessive Lutheran null phenotype, Lu(a-b-), of the Lutheran blood group. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2012]

RHCE Gene

Rh blood group, CcEe antigens

The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene which encodes both the RhC and RhE antigens on a single polypeptide and a second gene which encodes the RhD protein. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. A mutation in this gene results in amorph-type Rh-null disease. Alternative splicing of this gene results in four transcript variants encoding four different isoforms. [provided by RefSeq, Jul 2008]

body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated fasting blood glucose levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated fasting blood glucose levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Blood pressure measurement (high sodium intervention) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure measurement (high sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure measurement (cold pressor test) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure measurement (cold pressor test) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure measurement (high sodium and potassium intervention) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure measurement (high sodium and potassium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure measurement (low sodium intervention) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure measurement (low sodium intervention) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

fasting plasma glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting plasma glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma triglyceride and c-reactive protein, fasting glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma triglyceride and c-reactive protein, fasting glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting glucose-related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting glucose-related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Fasting plasma glucose Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting plasma glucose phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting glucose-related traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting glucose-related traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting glucose-related traits (interaction with BMI) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting glucose-related traits (interaction with BMI) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

[fasting plasma glucose level qtl 5] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 5] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 4] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 4] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 6] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 6] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

[fasting plasma glucose level qtl 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting plasma glucose level qtl 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; obesity; blood pressure, arterial; blood and blood forming organ disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

range of motion measurements Gene Set

From GAD Gene-Disease Associations

genes associated with the disease range of motion measurements in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

measurements Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term measurements in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

measurement Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term measurement in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Hormone measurements Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Hormone measurements phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (rim area) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (rim area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (cup area) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (cup area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (disc area) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (disc area) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Optic nerve measurement (cup-to-disc ratio) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Optic nerve measurement (cup-to-disc ratio) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Cardiac muscle measurement Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Cardiac muscle measurement phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

plasma glucose, basal hepatic glucose and increased insulin release Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose, basal hepatic glucose and increased insulin release in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Blood Glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Blood Glucose from the curated CTD Gene-Chemical Interactions dataset.

Blood Glucose Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Glucose in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; cholesterol, ldl; glucose tolerance; blood pressure, arterial; glycosylated hemoglobin a1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; cholesterol, ldl; glucose tolerance; blood pressure, arterial; glycosylated hemoglobin a1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; triglycerides; insulin; glucose; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial diabetes, type 2 glucose insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial diabetes, type 2 glucose insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; diabetes, type 2; insulin; glucose; insulin resistance; pc-1 protein content; systolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; blood pressure; body weight; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormality of blood glucose concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of blood glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

SIRT1-HNF4-alpha-PGC-1-alpha complex, in response to fasting Gene Set

From CORUM Protein Complexes

proteins in the SIRT1-HNF4-alpha-PGC-1-alpha complex, in response to fasting protein complex from the CORUM Protein Complexes dataset.

FASTING INSULIN LEVEL QUANTITATIVE TRAIT LOCUS 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease FASTING INSULIN LEVEL QUANTITATIVE TRAIT LOCUS 1 from the curated CTD Gene-Disease Associations dataset.

fasting total cholesterol and ldl-cholesterol concentrations only Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting total cholesterol and ldl-cholesterol concentrations only in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting plasma insulin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting plasma insulin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting insulin-related traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting insulin-related traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting insulin levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting insulin levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

impaired fasting glycemia and type 2 diabetes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease impaired fasting glycemia and type 2 diabetes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting insulin level Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fasting insulin level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fasting Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term fasting in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Fasting insulin-related traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting insulin-related traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting insulin (interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting insulin (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Fasting insulin-related traits (interaction with BMI) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Fasting insulin-related traits (interaction with BMI) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

fasting hyperinsulinemia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the fasting hyperinsulinemia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

fasting hypoglycemia Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the fasting hypoglycemia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

fasting hypoglycemia Gene Set

From HPO Gene-Disease Associations

genes associated with the fasting hypoglycemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

fasting hyperinsulinemia Gene Set

From HPO Gene-Disease Associations

genes associated with the fasting hyperinsulinemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

[fasting insulin level quantitative trait locus 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [fasting insulin level quantitative trait locus 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

blood pressure, oxidative stress levels in blood Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, oxidative stress levels in blood in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood and blood forming organ disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood and blood forming organ disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; blood coagulation disorders, inherited; recurrence; thromboembolism; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the renal response to blood flow involved in circulatory renin-angiotensin regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

abnormality of blood and blood-forming tissues Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood and blood-forming tissues phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood and blood-forming tissues Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of blood and blood-forming tissues phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Congenital glucose-galactose malabsorption Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital glucose-galactose malabsorption phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly, short stature, and impaired glucose metabolism Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly, short stature, and impaired glucose metabolism phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose-6-phosphate transport defect Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose-6-phosphate transport defect phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glucose transporter type 1 deficiency syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glucose transporter type 1 deficiency syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

2-deoxy-D-glucose-344 Gene Set

From CMAP Signatures of Differentially Expressed Genes for Small Molecules

genes differentially expressed following the 2-deoxy-D-glucose-344 small molecule perturbation from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.

Glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Glucose from the curated CTD Gene-Chemical Interactions dataset.

Glucose-6-Phosphate Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Glucose-6-Phosphate from the curated CTD Gene-Chemical Interactions dataset.

Uridine Diphosphate Glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical Uridine Diphosphate Glucose from the curated CTD Gene-Chemical Interactions dataset.

beta-penta-O-galloyl-glucose Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical beta-penta-O-galloyl-glucose from the curated CTD Gene-Chemical Interactions dataset.

glucose tolerance factor Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical glucose tolerance factor from the curated CTD Gene-Chemical Interactions dataset.

HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEMOLYTIC ANEMIA, NONSPHEROCYTIC, DUE TO GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Glucose Intolerance Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glucose Intolerance from the curated CTD Gene-Disease Associations dataset.

Glucose-Galactose Malabsorption Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glucose-Galactose Malabsorption from the curated CTD Gene-Disease Associations dataset.

Glucose Metabolism Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Glucose Metabolism Disorders from the curated CTD Gene-Disease Associations dataset.

Glucose Tolerance Test Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Glucose Tolerance Test in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Glucose Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Glucose in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Glucose Transporter Type 2 Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Glucose Transporter Type 2 in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

glucose metabolism disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease glucose metabolism disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

glucose metabolism disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease glucose metabolism disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

glucose intolerance Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease glucose intolerance in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

glucose metabolism disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease glucose metabolism disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

4-Deoxy-Alpha-D-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the 4-Deoxy-Alpha-D-Glucose drug from the curated DrugBank Drug Targets dataset.

4,6-Dideoxy-4-Amino-Alpha-D-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the 4,6-Dideoxy-4-Amino-Alpha-D-Glucose drug from the curated DrugBank Drug Targets dataset.

Alpha-D-Glucose-6-Phosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Alpha-D-Glucose-6-Phosphate drug from the curated DrugBank Drug Targets dataset.

2-Deoxy-2fluoro-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the 2-Deoxy-2fluoro-Glucose drug from the curated DrugBank Drug Targets dataset.

Glucose-6-Phosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Glucose-6-Phosphate drug from the curated DrugBank Drug Targets dataset.

Beta-D-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the Beta-D-Glucose drug from the curated DrugBank Drug Targets dataset.

Alpha-D-Glucose 1,6-Bisphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Alpha-D-Glucose 1,6-Bisphosphate drug from the curated DrugBank Drug Targets dataset.

6-Deoxy-Alpha-D-Glucose Gene Set

From DrugBank Drug Targets

interacting proteins for the 6-Deoxy-Alpha-D-Glucose drug from the curated DrugBank Drug Targets dataset.

Alpha-D-Glucose-1-Phosphate-6-Vanadate Gene Set

From DrugBank Drug Targets

interacting proteins for the Alpha-D-Glucose-1-Phosphate-6-Vanadate drug from the curated DrugBank Drug Targets dataset.

Glucose-Uridine-C1,5'-Diphosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Glucose-Uridine-C1,5'-Diphosphate drug from the curated DrugBank Drug Targets dataset.

Alpha-D-Glucose-1-Phosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the Alpha-D-Glucose-1-Phosphate drug from the curated DrugBank Drug Targets dataset.

2-Deoxy-Glucose-6-Phosphate Gene Set

From DrugBank Drug Targets

interacting proteins for the 2-Deoxy-Glucose-6-Phosphate drug from the curated DrugBank Drug Targets dataset.

breast neoplasms; endometrial neoplasms; glucose intolerance; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease breast neoplasms; endometrial neoplasms; glucose intolerance; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; lipids; atherosclerosis, generalized Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; lipids; atherosclerosis, generalized in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass diabetes, type 2 glucose insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass diabetes, type 2 glucose insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose response Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; glucose intolerance; prediabetic state Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance; prediabetic state in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; insulin; glucose; hba(1c) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; insulin; glucose; hba(1c) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma glucose levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; insulin; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; insulin; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance; obesity; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose intolerance; obesity; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; metabolic syndrome; hyperglycemia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; metabolic syndrome; hyperglycemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose transporter type 2 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose transporter type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; glucose intolerance; insulin resistance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; glucose intolerance; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; cholesterol, hdl; triglycerides; cholesterol, ldl; hypertension; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; cholesterol, hdl; triglycerides; cholesterol, ldl; hypertension; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; paraoxonase-1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; paraoxonase-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; insulin; glucose; c-peptide; fatty acid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; insulin; glucose; c-peptide; fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; vascular disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; vascular disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced serum c-peptide and insulin responses to an oral glucose challenge Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced serum c-peptide and insulin responses to an oral glucose challenge in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cerebral infarction; glucose intolerance; hyperhomocysteinemia; hyperlipidemias; hypertension in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; glucose intolerance; muscular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; glucose intolerance; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; triglycerides; glucose tolerance; beta-cell function; insulin; lipids Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; triglycerides; glucose tolerance; beta-cell function; insulin; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin in obese women with impaired glucose tolerance (igt) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin in obese women with impaired glucose tolerance (igt) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; lipids; obesity; glucose; leptin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; obesity; glucose; leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; birth weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose; hba1c Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 2 diabetes related glucose homeostasis trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease type 2 diabetes related glucose homeostasis trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; lipids; c-reactive protein; obesity; glucose; leptin; atopy Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; lipids; c-reactive protein; obesity; glucose; leptin; atopy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; glucose tolerance; insulin; hematology indices Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; glucose tolerance; insulin; hematology indices in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

undetectable glucose-6-phosphate dehydrogenase enzyme activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease undetectable glucose-6-phosphate dehydrogenase enzyme activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; body fat Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

triglycerides; insulin; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease triglycerides; insulin; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose intolerance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose; stroke; carotid artery intima-media thickness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; cholesterol, ldl; cholesterol, total; glucose; stroke; carotid artery intima-media thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

type 2 diabetes related glucose homeostasis traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease type 2 diabetes related glucose homeostasis traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; glucose; nervous system activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; glucose; nervous system activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; triglycerides; hypertension; glucose tolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; triglycerides; hypertension; glucose tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gastritis; glucose metabolism disorders; helicobacter infections; stomach neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gastritis; glucose metabolism disorders; helicobacter infections; stomach neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; insulin; glucose; body fat Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; insulin; glucose; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; lipids; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; lipids; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; lipids; glucose; cortisol; anthropometric parameters Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; glucose; cortisol; anthropometric parameters in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; lipids; obesity; glucose; leptin; cortisol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; obesity; glucose; leptin; cortisol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes or impaired glucose tolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes or impaired glucose tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; insulin secretion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose tolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose tolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin sensitivity; glucose disposal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin sensitivity; glucose disposal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; lipids; fibrinogen; hematology indices Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; lipids; fibrinogen; hematology indices in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; lipid metabolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; lipid metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; glucose; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; glucose; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose metabolism disorders; obesity; spinal dysraphism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose metabolism disorders; obesity; spinal dysraphism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced early insulin response to oral glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced early insulin response to oral glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose; insulin secretion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose; insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyslipidemias; glucose intolerance; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyslipidemias; glucose intolerance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; fatty acid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose-stimulated beta cell function Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose-stimulated beta cell function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose tolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; glucose intolerance; obesity; overweight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance; obesity; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose metabolism disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; glucose tolerance; insulin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; glucose tolerance; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; lipids; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; lipids; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; obesity; glucose; cortisol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; obesity; glucose; cortisol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; metabolic syndrome; adiponectin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; metabolic syndrome; adiponectin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; polycystic ovary syndrome; androgen levels; anthropometric measuments Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; polycystic ovary syndrome; androgen levels; anthropometric measuments in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance test Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance test in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin response to oral glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin response to oral glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; obesity; energy expenditure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; obesity; energy expenditure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; c-reactive protein; obesity; glucose; leptin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; c-reactive protein; obesity; glucose; leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; insulin; polycystic ovary syndrome; hormone disturbance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; insulin; polycystic ovary syndrome; hormone disturbance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; lactose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; lactose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity and glucose homeostasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity and glucose homeostasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus, type 2; glucose intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus, type 2; glucose intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; glucose tolerance; metabolic syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 2; glucose tolerance; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose tolerance; adiponectin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose tolerance; adiponectin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; glucose; c-peptide; fatty acid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; glucose; c-peptide; fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

two-hour glucose challenge Gene Set

From GAD Gene-Disease Associations

genes associated with the disease two-hour glucose challenge in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; diabetes, type 2; glucose; birth weight Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; diabetes, type 2; glucose; birth weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; glucose; c-peptide Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; glucose; c-peptide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

oral glucose tolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease oral glucose tolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; glucose; atherosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; glucose; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose; adiponectin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose; adiponectin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; diabetic angiopathies; diabetic neuropathies; diabetic retinopathy; glucose intolerance; hemochromatosis; liver cirrhosis; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; diabetic angiopathies; diabetic neuropathies; diabetic retinopathy; glucose intolerance; hemochromatosis; liver cirrhosis; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased serum glucose concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased serum glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; glucose intolerance; insulin resistance; polycystic ovarian syndrome; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma glucose concentration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma glucose concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; insulin; obesity; glucose Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; insulin; obesity; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; glucose tolerance; insulin; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; glucose tolerance; insulin; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose homeostasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glucose homeostasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cortisol escape from dexamethasone and elevated glucose levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cortisol escape from dexamethasone and elevated glucose levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

glucose Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term glucose in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

negative regulation of transcription by glucose Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of transcription by glucose biological process from the curated GO Biological Process Annotations dataset.

glucose-6-phosphate transport Gene Set

From GO Biological Process Annotations

genes participating in the glucose-6-phosphate transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of udp-glucose catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of udp-glucose catabolic process biological process from the curated GO Biological Process Annotations dataset.

response to glucose Gene Set

From GO Biological Process Annotations

genes participating in the response to glucose biological process from the curated GO Biological Process Annotations dataset.

negative regulation of transcription from rna polymerase ii promoter by glucose Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of transcription from rna polymerase ii promoter by glucose biological process from the curated GO Biological Process Annotations dataset.

udp-glucose catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the udp-glucose catabolic process biological process from the curated GO Biological Process Annotations dataset.

glucose 6-phosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the glucose 6-phosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of insulin secretion involved in cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the regulation of insulin secretion involved in cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

insulin secretion involved in cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the insulin secretion involved in cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

positive regulation of transcription by glucose Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of transcription by glucose biological process from the curated GO Biological Process Annotations dataset.

glucose metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the glucose metabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of glucose import Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of glucose import biological process from the curated GO Biological Process Annotations dataset.

regulation of detection of glucose Gene Set

From GO Biological Process Annotations

genes participating in the regulation of detection of glucose biological process from the curated GO Biological Process Annotations dataset.

positive regulation of glucose transport Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of glucose transport biological process from the curated GO Biological Process Annotations dataset.

glucose catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the glucose catabolic process biological process from the curated GO Biological Process Annotations dataset.

cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

negative regulation of glucose transport Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of glucose transport biological process from the curated GO Biological Process Annotations dataset.

negative regulation of insulin secretion involved in cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of insulin secretion involved in cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

positive regulation of transcription from rna polymerase ii promoter by glucose Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of transcription from rna polymerase ii promoter by glucose biological process from the curated GO Biological Process Annotations dataset.

positive regulation of glucose import in response to insulin stimulus Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of glucose import in response to insulin stimulus biological process from the curated GO Biological Process Annotations dataset.

negative regulation of glucose import Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of glucose import biological process from the curated GO Biological Process Annotations dataset.

negative regulation of glucose import in response to insulin stimulus Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of glucose import in response to insulin stimulus biological process from the curated GO Biological Process Annotations dataset.

glucose mediated signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the glucose mediated signaling pathway biological process from the curated GO Biological Process Annotations dataset.

glucose import Gene Set

From GO Biological Process Annotations

genes participating in the glucose import biological process from the curated GO Biological Process Annotations dataset.

regulation of glucose transport Gene Set

From GO Biological Process Annotations

genes participating in the regulation of glucose transport biological process from the curated GO Biological Process Annotations dataset.

glucose transport Gene Set

From GO Biological Process Annotations

genes participating in the glucose transport biological process from the curated GO Biological Process Annotations dataset.

cellular response to glucose starvation Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to glucose starvation biological process from the curated GO Biological Process Annotations dataset.

glucose 1-phosphate metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the glucose 1-phosphate metabolic process biological process from the curated GO Biological Process Annotations dataset.

cellular glucose homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the cellular glucose homeostasis biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription by glucose Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription by glucose biological process from the curated GO Biological Process Annotations dataset.

regulation of udp-glucose catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of udp-glucose catabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of glucose import in response to insulin stimulus Gene Set

From GO Biological Process Annotations

genes participating in the regulation of glucose import in response to insulin stimulus biological process from the curated GO Biological Process Annotations dataset.

udp-glucose metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the udp-glucose metabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of insulin secretion involved in cellular response to glucose stimulus Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of insulin secretion involved in cellular response to glucose stimulus biological process from the curated GO Biological Process Annotations dataset.

detection of glucose Gene Set

From GO Biological Process Annotations

genes participating in the detection of glucose biological process from the curated GO Biological Process Annotations dataset.

renal glucose absorption Gene Set

From GO Biological Process Annotations

genes participating in the renal glucose absorption biological process from the curated GO Biological Process Annotations dataset.

regulation of glucose import Gene Set

From GO Biological Process Annotations

genes participating in the regulation of glucose import biological process from the curated GO Biological Process Annotations dataset.

regulation of transcription from rna polymerase ii promoter by glucose Gene Set

From GO Biological Process Annotations

genes participating in the regulation of transcription from rna polymerase ii promoter by glucose biological process from the curated GO Biological Process Annotations dataset.

negative regulation of detection of glucose Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of detection of glucose biological process from the curated GO Biological Process Annotations dataset.

regulation of gluconeogenesis involved in cellular glucose homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of gluconeogenesis involved in cellular glucose homeostasis biological process from the curated GO Biological Process Annotations dataset.

regulation of glucose metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of glucose metabolic process biological process from the curated GO Biological Process Annotations dataset.

glucose homeostasis Gene Set

From GO Biological Process Annotations

genes participating in the glucose homeostasis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of glucose metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of glucose metabolic process biological process from the curated GO Biological Process Annotations dataset.

udp-glucose 6-dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-glucose 6-dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

glycogen synthase activity, transferring glucose-1-phosphate Gene Set

From GO Molecular Function Annotations

genes performing the glycogen synthase activity, transferring glucose-1-phosphate molecular function from the curated GO Molecular Function Annotations dataset.

glucose binding Gene Set

From GO Molecular Function Annotations

genes performing the glucose binding molecular function from the curated GO Molecular Function Annotations dataset.

glucose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose 1-dehydrogenase [nad(p)] activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose 1-dehydrogenase [nad(p)] activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-6-phosphate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-6-phosphate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

d-glucose transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the d-glucose transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose:sodium symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose:sodium symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-6-phosphate dehydrogenase activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-6-phosphate dehydrogenase activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-glucose:glycoprotein glucosyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-glucose:glycoprotein glucosyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-glucose:hexose-1-phosphate uridylyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-glucose:hexose-1-phosphate uridylyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

udp-glucose 4-epimerase activity Gene Set

From GO Molecular Function Annotations

genes performing the udp-glucose 4-epimerase activity molecular function from the curated GO Molecular Function Annotations dataset.

gdp-d-glucose phosphorylase activity Gene Set

From GO Molecular Function Annotations

genes performing the gdp-d-glucose phosphorylase activity molecular function from the curated GO Molecular Function Annotations dataset.

utp:glucose-1-phosphate uridylyltransferase activity Gene Set

From GO Molecular Function Annotations

genes performing the utp:glucose-1-phosphate uridylyltransferase activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-1,6-bisphosphate synthase activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-1,6-bisphosphate synthase activity molecular function from the curated GO Molecular Function Annotations dataset.

low-affinity glucose:sodium symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the low-affinity glucose:sodium symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

dtdp-glucose 4,6-dehydratase activity Gene Set

From GO Molecular Function Annotations

genes performing the dtdp-glucose 4,6-dehydratase activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-6-phosphate isomerase activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-6-phosphate isomerase activity molecular function from the curated GO Molecular Function Annotations dataset.

glucose-6-phosphatase activity Gene Set

From GO Molecular Function Annotations

genes performing the glucose-6-phosphatase activity molecular function from the curated GO Molecular Function Annotations dataset.

UDP-glucose Gene Set

From Guide to Pharmacology Chemical Ligands of Receptors

receptors of the UDP-glucose ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset.

Two-hour glucose challenge Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Two-hour glucose challenge phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

glucose metabolism disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease glucose metabolism disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

abnormal glucose homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

dTDP-D-glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the dTDP-D-glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Glucose 1-phosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Glucose 1-phosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Beta-D-Glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Beta-D-Glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Glucose 6-phosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Glucose 6-phosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

D-Gal alpha 1->6D-Gal alpha 1->6D-Glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the D-Gal alpha 1->6D-Gal alpha 1->6D-Glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Uridine diphosphate glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Uridine diphosphate glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

4,6-Dideoxy-4-oxo-dTDP-D-glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the 4,6-Dideoxy-4-oxo-dTDP-D-glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Beta-D-Glucose 6-phosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Beta-D-Glucose 6-phosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

Alpha-D-Glucose 1,6-bisphosphate Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Alpha-D-Glucose 1,6-bisphosphate metabolite from the curated HMDB Metabolites of Enzymes dataset.

D-Glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the D-Glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

Alpha-D-Glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the Alpha-D-Glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

GDP-glucose Gene Set

From HMDB Metabolites of Enzymes

interacting proteins for the GDP-glucose metabolite from the curated HMDB Metabolites of Enzymes dataset.

abnormal glucose homeostasis Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal glucose homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

glucose intolerance Gene Set

From HPO Gene-Disease Associations

genes associated with the glucose intolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of urine glucose concentration Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of urine glucose concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal oral glucose tolerance Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal oral glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal glucose tolerance Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Glucose Intolerance Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Glucose Intolerance phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Glucose Metabolism Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Glucose Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

GDP-glucose biosynthesis II Gene Set

From HumanCyc Pathways

proteins participating in the GDP-glucose biosynthesis II pathway from the HumanCyc Pathways dataset.

Glucose-6-phosphate dehydrogenase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphate dehydrogenase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-dependent insulinotropic receptor Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-dependent insulinotropic receptor protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-inhibited division protein A-related, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-inhibited division protein A-related, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose 4-epimerase GalE Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose 4-epimerase GalE protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose/GDP-mannose dehydrogenase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose/GDP-mannose dehydrogenase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 2 (GLUT2) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 2 (GLUT2) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-6-phosphate dehydrogenase, NAD-binding Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphate dehydrogenase, NAD-binding protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 3 (GLUT3) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 3 (GLUT3) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose:Glycoprotein Glucosyltransferase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose:Glycoprotein Glucosyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose/GDP-mannose dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose/GDP-mannose dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose/Sorbosone dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose/Sorbosone dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose/GDP-mannose dehydrogenase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose/GDP-mannose dehydrogenase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-6-phosphate dehydrogenase, active site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphate dehydrogenase, active site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

dTDP-glucose 4,6-dehydratase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the dTDP-glucose 4,6-dehydratase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose/GDP-mannose dehydrogenase, dimerisation Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose/GDP-mannose dehydrogenase, dimerisation protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Aldose 1-/Glucose-6-phosphate 1-epimerase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Aldose 1-/Glucose-6-phosphate 1-epimerase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase, C-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

GDP-L-galactose/GDP-D-glucose phosphorylase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the GDP-L-galactose/GDP-D-glucose phosphorylase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose 4-epimerase C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose 4-epimerase C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UTP--glucose-1-phosphate uridylyltransferase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UTP--glucose-1-phosphate uridylyltransferase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose/ribitol dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose/ribitol dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 1 (GLUT1) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 1 (GLUT1) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UTP--glucose-1-phosphate uridylyltransferase family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UTP--glucose-1-phosphate uridylyltransferase family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-6-phosphate dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphate dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase, N-terminal Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Soluble quinoprotein glucose/sorbosone dehydrogenase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Soluble quinoprotein glucose/sorbosone dehydrogenase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose transporter, type 4 (GLUT4) Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose transporter, type 4 (GLUT4) protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-methanol-choline oxidoreductase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-methanol-choline oxidoreductase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

UDP-glucose 6-dehydrogenase, eukaryotic type Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the UDP-glucose 6-dehydrogenase, eukaryotic type protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-inhibited division protein A-related Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-inhibited division protein A-related protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Glucose-6-phosphatase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Glucose-6-phosphatase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal muscle cell glucose uptake Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal muscle cell glucose uptake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased urine glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased urine glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal renal glucose reabsorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal renal glucose reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal glucose homeostasis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal glucose homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cellular glucose import Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cellular glucose import phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal glucose absorption Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal glucose absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal glucose tolerance Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal glucose tolerance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired cellular glucose import Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired cellular glucose import phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

enhanced cellular glucose import Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the enhanced cellular glucose import phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired glucose tolerance Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the impaired glucose tolerance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urine glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urine glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal adipocyte glucose uptake Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal adipocyte glucose uptake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal cardiac cell glucose uptake Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal cardiac cell glucose uptake phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

improved glucose tolerance Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the improved glucose tolerance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased fasted circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal fasted circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased fasted circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased fasted circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased circulating glucose level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased circulating glucose level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

glucose/galactose malabsorption Gene Set

From OMIM Gene-Disease Associations

genes associated with the glucose/galactose malabsorption phenotype from the curated OMIM Gene-Disease Associations dataset.

[plasma glucose, 2-hour, qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [plasma glucose, 2-hour, qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly, short stature, and impaired glucose metabolism Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly, short stature, and impaired glucose metabolism phenotype from the curated OMIM Gene-Disease Associations dataset.

[plasma glucose, 2-hour, qtl 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [plasma glucose, 2-hour, qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

p53 pathway by glucose deprivation Gene Set

From PANTHER Pathways

proteins participating in the p53 pathway by glucose deprivation pathway from the PANTHER Pathways dataset.

glucose Gene Set

From Phosphosite Textmining Biological Term Annotations

proteins co-occuring with the biological term glucose in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset.

Insulin-mediated glucose transport Gene Set

From PID Pathways

proteins participating in the Insulin-mediated glucose transport pathway from the PID Pathways dataset.

Synthesis of dolichyl-phosphate-glucose Gene Set

From Reactome Pathways

proteins participating in the Synthesis of dolichyl-phosphate-glucose pathway from the Reactome Pathways dataset.

Glucose metabolism Gene Set

From Reactome Pathways

proteins participating in the Glucose metabolism pathway from the Reactome Pathways dataset.

Na+-dependent glucose transporters Gene Set

From Reactome Pathways

proteins participating in the Na+-dependent glucose transporters pathway from the Reactome Pathways dataset.

Glucose transport Gene Set

From Reactome Pathways

proteins participating in the Glucose transport pathway from the Reactome Pathways dataset.

Facilitative Na+-independent glucose transporters Gene Set

From Reactome Pathways

proteins participating in the Facilitative Na+-independent glucose transporters pathway from the Reactome Pathways dataset.

Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds Gene Set

From Reactome Pathways

proteins participating in the Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds pathway from the Reactome Pathways dataset.

Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) Gene Set

From Reactome Pathways

proteins participating in the Synthesis, secretion, and inactivation of Glucose-dependent Insulinotropic Polypeptide (GIP) pathway from the Reactome Pathways dataset.

Blood group, john milton hagen system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, john milton hagen system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--WALDNER TYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--WALDNER TYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the ABO BLOOD GROUP SYSTEM, B(A) PHENOTYPE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cromer blood group system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cromer blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Radin blood group Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Radin blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, junior system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, junior system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, gerbich system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, gerbich system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Adult i Blood Group with or without Congenital Cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Adult i Blood Group with or without Congenital Cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--OK Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--OK phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Antigen in Scianna blood group system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Antigen in Scianna blood group system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Langereis blood group Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Langereis blood group phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--FROESE Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--FROESE phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--LUTHERAN INHIBITOR Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--LUTHERAN INHIBITOR phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood group, dombrock system Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Blood group, dombrock system phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BLOOD GROUP--WRIGHT ANTIGEN Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the BLOOD GROUP--WRIGHT ANTIGEN phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

blood microparticle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the blood microparticle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

blood microparticle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the blood microparticle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

dragon's blood Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical dragon's blood from the curated CTD Gene-Chemical Interactions dataset.

Blood Loss, Surgical Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blood Loss, Surgical from the curated CTD Gene-Disease Associations dataset.

Blood Coagulation Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blood Coagulation Disorders from the curated CTD Gene-Disease Associations dataset.

Blood Platelet Disorders Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blood Platelet Disorders from the curated CTD Gene-Disease Associations dataset.

PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PLASMODIUM FALCIPARUM BLOOD INFECTION LEVEL from the curated CTD Gene-Disease Associations dataset.

Blood Coagulation Disorders, Inherited Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Blood Coagulation Disorders, Inherited from the curated CTD Gene-Disease Associations dataset.

Blood Viscosity Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Viscosity in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Cells Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Cells in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Proteins Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Proteins in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Urea Nitrogen Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Urea Nitrogen in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Coagulation Factors Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Coagulation Factors in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Pressure Determination Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Pressure Determination in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Sedimentation Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Sedimentation in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Flow Velocity Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Flow Velocity in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Vessels Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Vessels in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Pressure Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Pressure in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Blood Coagulation Factor Inhibitors Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait Blood Coagulation Factor Inhibitors in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

blood platelet disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease blood platelet disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

blood protein disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease blood protein disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

blood coagulation disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease blood coagulation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

inherited blood coagulation disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease inherited blood coagulation disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

blood coagulation disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease blood coagulation disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

blood group incompatibility Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blood group incompatibility in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

inherited blood coagulation disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease inherited blood coagulation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

autoimmune disease of blood Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease autoimmune disease of blood in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

blood platelet disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blood platelet disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

blood protein disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blood protein disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

blood coagulation disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease blood coagulation disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

blood platelet disorders; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood platelet disorders; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl/blood* Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl/blood* in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood group incompatibility; rh isoimmunization Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood group incompatibility; rh isoimmunization in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; heart rate; orthostatic intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; heart rate; orthostatic intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

baroreflex and blood pressure regulation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease baroreflex and blood pressure regulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure; aldosterone; glomerular filtration rate; renal plasma flow Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; aldosterone; glomerular filtration rate; renal plasma flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; protein c deficiency; protein s deficiency; thrombophilia; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; protein c deficiency; protein s deficiency; pulmonary embolism; pulmonary embolisms; thrombosis; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; left ventricular function; blood pressure; left ventricular structure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; left ventricular function; blood pressure; left ventricular structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

triglycerides; blood pressure, arterial; antioxidant activity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease triglycerides; blood pressure, arterial; antioxidant activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure; heart rate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; heart rate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular hypertrophy; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular hypertrophy; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; cardiovascular diseases; optic neuropathy, ischemic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease atrial fibrillation; blood loss, surgical; coronary disease; coronary heart disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; pulmonary embolism; venous thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; carotid atherosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; carotid atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anxiety disorder; blood pressure, arterial; memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anxiety disorder; blood pressure, arterial; memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; diabetes, type 2; blood pressure, arterial; liver disease; periodontitis; acenocoumarol response; acetaldehyde; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; diabetes, type 2; blood pressure, arterial; liver disease; periodontitis; acenocoumarol response; acetaldehyde; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood urea nitrogen Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood urea nitrogen in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; blood coagulation disorders; liver diseases; protein c deficiency; protein s deficiency; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation factors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation factors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood catalase levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood catalase levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; arterial wall changes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; arterial wall changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; puerperal disorders; sinus thrombosis, intracranial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; inflammation; nervous system diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; inflammation; nervous system diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lead blood levels; zinc Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lead blood levels; zinc in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; triglycerides; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; triglycerides; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antiphospholipid syndrome; arterial occlusive diseases; blood coagulation disorders, inherited; cardiomyopathy, dilated; heart defects, congenital; heart diseases; thrombophilia; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood loss, surgical Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood loss, surgical in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood viscosity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood viscosity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; osteonecrosis; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; osteonecrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; left ventricular mass Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; left ventricular mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; triglycerides; hypertension; blood pressure, arterial; potassium; urea Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; triglycerides; hypertension; blood pressure, arterial; potassium; urea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; hypertension; c-reactive protein; fibrinogen; homocysteine; white blood cell count in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anoxia; blood coagulation disorders, inherited; heart defects, congenital; infection; polycythemia; postoperative complications; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; blood coagulation disorders, inherited; femur head necrosis; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood flow; vascular response; oxidative stress; nitirc oxide production; nitric oxide-mediated effect on resistance vessels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood sedimentation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood sedimentation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

systolic blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease systolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood flow velocity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood flow velocity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood lipids and maximal oxygen uptake Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood lipids and maximal oxygen uptake in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipids; blood pressure; atherosclerosis, carotid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipids; blood pressure; atherosclerosis, carotid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure determination Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure determination in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lymphoproliferative disorders; blood transfusion complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphoproliferative disorders; blood transfusion complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary blood flow Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary blood flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

macroangiopathy and blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease macroangiopathy and blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood transfusion Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood transfusion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; blood pressure, arterial; nitric oxide production; salt sensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; blood pressure, arterial; nitric oxide production; salt sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ace concentration and blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease ace concentration and blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

progression of carotid atherosclerosis blood pressure and serum lipids Gene Set

From GAD Gene-Disease Associations

genes associated with the disease progression of carotid atherosclerosis blood pressure and serum lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation factor inhibitors Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation factor inhibitors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; blood pressure, arterial; stroke; longevity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; blood pressure, arterial; stroke; longevity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adiposity and blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adiposity and blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood platelet disorders; cardiovascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood platelet disorders; cardiovascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; sodium hemostatis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; sodium hemostatis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; renin activity; aldosterone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; renin activity; aldosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; blood pressure, arterial; sleep apnea Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; blood pressure, arterial; sleep apnea in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 1; blood group incompatibility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 1; blood group incompatibility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

preeclampsia; blood pressure; endothelin-1 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease preeclampsia; blood pressure; endothelin-1 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; adiponectin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; adiponectin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

birth weight; cord blood igf-ii levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease birth weight; cord blood igf-ii levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

left ventricular hypertrophy; blood flow; left ventricular function Gene Set

From GAD Gene-Disease Associations

genes associated with the disease left ventricular hypertrophy; blood flow; left ventricular function in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

i/d ace gene polymorphism and abo blood group system Gene Set

From GAD Gene-Disease Associations

genes associated with the disease i/d ace gene polymorphism and abo blood group system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; blood pressure, arterial; acetaldehyde; lipid peroxide Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; blood pressure, arterial; acetaldehyde; lipid peroxide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nephropathy, diabetic; blood pressure, arterial; proteinuria Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nephropathy, diabetic; blood pressure, arterial; proteinuria in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; cystic fibrosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; cystic fibrosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; lipids; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; lipids; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol, hdl; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol, hdl; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; legg-perthes disease; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; legg-perthes disease; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood proteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood proteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; insulin; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

folic acid in plasma and red blood cell folate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease folic acid in plasma and red blood cell folate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; hypertension, pulmonary; pulmonary embolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

decreased blood pressure and plasma triglycerides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease decreased blood pressure and plasma triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced intrapartum blood loss--a possible evolutionary selection mechanism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced intrapartum blood loss--a possible evolutionary selection mechanism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta thalassemia; beta-thalassemia; blood coagulation disorders, inherited; sickle cell anemia; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood transfusion complications Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood transfusion complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; heart rate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; heart rate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

higher blood pressure after hospitalization in normotensi Gene Set

From GAD Gene-Disease Associations

genes associated with the disease higher blood pressure after hospitalization in normotensi in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; nitric oxide production; salt sensitivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; nitric oxide production; salt sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sleep disorders; body mass; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sleep disorders; body mass; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood dioxin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood dioxin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood flow Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood flow in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; atherosclerosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood lead concentration in children. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood lead concentration in children. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure phenotypes. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure phenotypes. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure; hyperlipidemia, familial combined Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; hyperlipidemia, familial combined in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure; aldosterone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure; aldosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 1; blood pressure, arterial; nephropathy in other diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes, type 1; blood pressure, arterial; nephropathy in other diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diastolic blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diastolic blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood cells Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood cells in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

arthritis; cholesterol, hdl; diabetes, type 2; osteoarthritis; blood pressure, arterial; liver disease; acetaldehyde; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; cholesterol, hdl; diabetes, type 2; osteoarthritis; blood pressure, arterial; liver disease; acetaldehyde; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, spontaneous; abruptio placentae; blood coagulation disorders, inherited; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sex steroid hormone blood levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease sex steroid hormone blood levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood pressure, arterial; heart rate; adrenaline; coronary flow velocity; ecg; noradrenaline Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood pressure, arterial; heart rate; adrenaline; coronary flow velocity; ecg; noradrenaline in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; diabetes, type 2; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; diabetes, type 2; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders; eclampsia; hellp syndrome; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood vessels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood vessels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood tacrolimus concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood tacrolimus concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; insulin; obesity; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; insulin; obesity; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood coagulation disorders, inherited; myocardial infarction Gene Set

From GAD Gene-Disease Associations

genes associated with the disease blood coagulation disorders, inherited; myocardial infarction in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated blood pressure and personality disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated blood pressure and personality disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

c-reactive protein blood levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease c-reactive protein blood levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease activated protein c resistance; beta-thalassemia; blood coagulation disorders; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; triglycerides; blood pressure Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; triglycerides; blood pressure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass; cholesterol; cholesterol, hdl; triglycerides; blood pressure; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol abuse; blood pressure, arterial Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol abuse; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass index, blood pressure and cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body mass index, blood pressure and cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apnea; apoplexy; blood coagulation disorders; brain ischemia; cerebrovascular disorders; hypotony, muscle; muscle hypotonia; protein c deficiency; seizures; stroke; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term blood in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Severe acute respiratory syndrome (SARS)_Peripheral blood mononuclear cell_GSE1739 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

LGLL - Large granular lymphocytic leukemia_Peripheral blood mononuclear cell_GSE10631 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during LGLL - Large granular lymphocytic leukemia_Peripheral blood mononuclear cell_GSE10631 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Bacterial Infection_Peripheral blood mononuclear cell_GSE3026 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Bacterial Infection_Peripheral blood mononuclear cell_GSE3026 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Pauciarticular juvenile arthritis_Peripheral blood mononuclear cell_GSE1402 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Pauciarticular juvenile arthritis_Peripheral blood mononuclear cell_GSE1402 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

HIV - Human immunodeficiency virus infection_Peripheral blood mononuclear cell_GSE2171 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during HIV - Human immunodeficiency virus infection_Peripheral blood mononuclear cell_GSE2171 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during B-cell chronic lymphocytic leukaemia-small lymphocytic lymphoma_Peripheral blood mononuclear cell_GSE8835 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

PTSD - Post-traumatic stress disorder_Peripheral blood mononuclear cell_GSE860 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during PTSD - Post-traumatic stress disorder_Peripheral blood mononuclear cell_GSE860 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Ulcerative Colitis_Peripheral blood mononuclear cell_GSE3365 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Ulcerative Colitis_Peripheral blood mononuclear cell_GSE3365 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

Rotavirus infection of children_Peripheral blood mononuclear cell_GSE2729 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during Rotavirus infection of children_Peripheral blood mononuclear cell_GSE2729 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

JRA - Juvenile rheumatoid arthritis_Peripheral blood mononuclear cell_GSE7753 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during JRA - Juvenile rheumatoid arthritis_Peripheral blood mononuclear cell_GSE7753 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

PFKL_OE_GDS3353_76_human_B cells in blood Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the PFKL_OE_GDS3353_76_human_B cells in blood gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

negative regulation of heart rate involved in baroreceptor response to increased systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of heart rate involved in baroreceptor response to increased systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

norepinephrine-epinephrine vasoconstriction involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the norepinephrine-epinephrine vasoconstriction involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

positive regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell differentiation Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell differentiation biological process from the curated GO Biological Process Annotations dataset.

apoptotic process involved in patterning of blood vessels Gene Set

From GO Biological Process Annotations

genes participating in the apoptotic process involved in patterning of blood vessels biological process from the curated GO Biological Process Annotations dataset.

positive regulation of lipid transport across blood brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations dataset.

regulation of blood coagulation, intrinsic pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood coagulation, intrinsic pathway biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell fate commitment Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell fate commitment biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood coagulation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood coagulation biological process from the curated GO Biological Process Annotations dataset.

vasodilation of artery involved in baroreceptor response to increased systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasodilation of artery involved in baroreceptor response to increased systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of blood microparticle formation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood microparticle formation biological process from the curated GO Biological Process Annotations dataset.

renin secretion into blood stream Gene Set

From GO Biological Process Annotations

genes participating in the renin secretion into blood stream biological process from the curated GO Biological Process Annotations dataset.

establishment of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel development biological process from the curated GO Biological Process Annotations dataset.

retinal blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the retinal blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

venous blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the venous blood vessel development biological process from the curated GO Biological Process Annotations dataset.

regulation of blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel size Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel size biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

labyrinthine layer blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the labyrinthine layer blood vessel development biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell migration involved in intussusceptive angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell migration involved in intussusceptive angiogenesis biological process from the curated GO Biological Process Annotations dataset.

establishment of glial blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of glial blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

venous blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the venous blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

establishment of blood-nerve barrier Gene Set

From GO Biological Process Annotations

genes participating in the establishment of blood-nerve barrier biological process from the curated GO Biological Process Annotations dataset.

renal system process involved in regulation of blood volume Gene Set

From GO Biological Process Annotations

genes participating in the renal system process involved in regulation of blood volume biological process from the curated GO Biological Process Annotations dataset.

angiotensin mediated vasoconstriction involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the angiotensin mediated vasoconstriction involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

maintenance of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the maintenance of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

blood coagulation, extrinsic pathway Gene Set

From GO Biological Process Annotations

genes participating in the blood coagulation, extrinsic pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of lipid transport across blood brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations dataset.

negative regulation of establishment of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of establishment of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

blood vessel lumenization Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel lumenization biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of establishment of blood-brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the regulation of establishment of blood-brain barrier biological process from the curated GO Biological Process Annotations dataset.

negative regulation of testicular blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of testicular blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure mediated by a chemical signal Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure mediated by a chemical signal biological process from the curated GO Biological Process Annotations dataset.

regulation of blood volume by renal aldosterone Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood volume by renal aldosterone biological process from the curated GO Biological Process Annotations dataset.

placenta blood vessel development Gene Set

From GO Biological Process Annotations

genes participating in the placenta blood vessel development biological process from the curated GO Biological Process Annotations dataset.

blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the renal control of peripheral vascular resistance involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by vasopressin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by vasopressin biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

regulation of blood circulation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood circulation biological process from the curated GO Biological Process Annotations dataset.

detection of hypoxic conditions in blood by carotid body chemoreceptor signaling Gene Set

From GO Biological Process Annotations

genes participating in the detection of hypoxic conditions in blood by carotid body chemoreceptor signaling biological process from the curated GO Biological Process Annotations dataset.

vasodilation by angiotensin involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasodilation by angiotensin involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel size by renin-angiotensin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel size by renin-angiotensin biological process from the curated GO Biological Process Annotations dataset.

regulation of blood coagulation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood coagulation biological process from the curated GO Biological Process Annotations dataset.

vasodilation by acetylcholine involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasodilation by acetylcholine involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood circulation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood circulation biological process from the curated GO Biological Process Annotations dataset.

blood vessel endothelial cell fate specification Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel endothelial cell fate specification biological process from the curated GO Biological Process Annotations dataset.

blood coagulation Gene Set

From GO Biological Process Annotations

genes participating in the blood coagulation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of renin secretion into blood stream Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of renin secretion into blood stream biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by atrial natriuretic peptide Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by atrial natriuretic peptide biological process from the curated GO Biological Process Annotations dataset.

regulation of blood volume by renin-angiotensin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood volume by renin-angiotensin biological process from the curated GO Biological Process Annotations dataset.

negative regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

vasoconstriction of artery involved in ischemic response to lowering of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasoconstriction of artery involved in ischemic response to lowering of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of the force of heart contraction involved in baroreceptor response to increased systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of the force of heart contraction involved in baroreceptor response to increased systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

vasodilation by norepinephrine-epinephrine involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasodilation by norepinephrine-epinephrine involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by circulatory renin-angiotensin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by circulatory renin-angiotensin biological process from the curated GO Biological Process Annotations dataset.

blood coagulation, intrinsic pathway Gene Set

From GO Biological Process Annotations

genes participating in the blood coagulation, intrinsic pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood microparticle formation Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood microparticle formation biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by endothelin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by endothelin biological process from the curated GO Biological Process Annotations dataset.

patterning of blood vessels Gene Set

From GO Biological Process Annotations

genes participating in the patterning of blood vessels biological process from the curated GO Biological Process Annotations dataset.

activation of blood coagulation via clotting cascade Gene Set

From GO Biological Process Annotations

genes participating in the activation of blood coagulation via clotting cascade biological process from the curated GO Biological Process Annotations dataset.

regulation of renin secretion into blood stream Gene Set

From GO Biological Process Annotations

genes participating in the regulation of renin secretion into blood stream biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood vessel endothelial cell proliferation involved in sprouting angiogenesis biological process from the curated GO Biological Process Annotations dataset.

angiotensin catabolic process in blood Gene Set

From GO Biological Process Annotations

genes participating in the angiotensin catabolic process in blood biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by renin-angiotensin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by renin-angiotensin biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by hormone Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by hormone biological process from the curated GO Biological Process Annotations dataset.

detection of hypoxic conditions in blood by chemoreceptor signaling Gene Set

From GO Biological Process Annotations

genes participating in the detection of hypoxic conditions in blood by chemoreceptor signaling biological process from the curated GO Biological Process Annotations dataset.

blood circulation Gene Set

From GO Biological Process Annotations

genes participating in the blood circulation biological process from the curated GO Biological Process Annotations dataset.

blood vessel maturation Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel maturation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood pressure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of renin secretion into blood stream Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of renin secretion into blood stream biological process from the curated GO Biological Process Annotations dataset.

neurological system process involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the neurological system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by ischemic conditions Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by ischemic conditions biological process from the curated GO Biological Process Annotations dataset.

regulation of blood vessel remodeling Gene Set

From GO Biological Process Annotations

genes participating in the regulation of blood vessel remodeling biological process from the curated GO Biological Process Annotations dataset.

phosphatidylserine exposure on blood platelet Gene Set

From GO Biological Process Annotations

genes participating in the phosphatidylserine exposure on blood platelet biological process from the curated GO Biological Process Annotations dataset.

lipid transport across blood brain barrier Gene Set

From GO Biological Process Annotations

genes participating in the lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by aortic arch baroreceptor feedback biological process from the curated GO Biological Process Annotations dataset.

regulation of lung blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lung blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

regulation of systemic arterial blood pressure by baroreceptor feedback Gene Set

From GO Biological Process Annotations

genes participating in the regulation of systemic arterial blood pressure by baroreceptor feedback biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood vessel endothelial cell migration Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood vessel endothelial cell migration biological process from the curated GO Biological Process Annotations dataset.

blood vessel morphogenesis Gene Set

From GO Biological Process Annotations

genes participating in the blood vessel morphogenesis biological process from the curated GO Biological Process Annotations dataset.

positive regulation of blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of blood pressure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood coagulation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood coagulation biological process from the curated GO Biological Process Annotations dataset.

blood coagulation, common pathway Gene Set

From GO Biological Process Annotations

genes participating in the blood coagulation, common pathway biological process from the curated GO Biological Process Annotations dataset.

vasoconstriction of artery involved in baroreceptor response to lowering of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the vasoconstriction of artery involved in baroreceptor response to lowering of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

negative regulation of blood circulation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of blood circulation biological process from the curated GO Biological Process Annotations dataset.

renal system process involved in regulation of systemic arterial blood pressure Gene Set

From GO Biological Process Annotations

genes participating in the renal system process involved in regulation of systemic arterial blood pressure biological process from the curated GO Biological Process Annotations dataset.

blood microparticle Gene Set

From GO Cellular Component Annotations

proteins localized to the blood microparticle cellular component from the curated GO Cellular Component Annotations dataset.

blood vessel Gene Set

From GTEx Tissue Gene Expression Profiles

genes with high or low expression in blood vessel relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.

blood Gene Set

From GTEx Tissue Gene Expression Profiles

genes with high or low expression in blood relative to other tissues from the GTEx Tissue Gene Expression Profiles dataset.

Diastolic blood pressure Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Diastolic blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Triglycerides-Blood Pressure (TG-BP) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Triglycerides-Blood Pressure (TG-BP) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

White blood cell count Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Diastolic blood pressure (alcohol consumption interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Diastolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

White blood cell types Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the White blood cell types phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Red blood cell traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red blood cell traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Systolic blood pressure in sickle cell anemia Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Systolic blood pressure in sickle cell anemia phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood metabolite levels Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood metabolite levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure (age interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure (age interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

C-reactive protein and white blood cell count Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the C-reactive protein and white blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Obesity and blood pressure Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Obesity and blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood trace element (Se levels) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood trace element (Se levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood metabolite ratios Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood metabolite ratios phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood pressure Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Systolic blood pressure (alcohol consumption interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Systolic blood pressure (alcohol consumption interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood trace element (Zn levels) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood trace element (Zn levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Systolic blood pressure Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Systolic blood pressure phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Red blood cell count Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Red blood cell count phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Response to methylphenidate treatment in attention-deficit/hyperactivity disorder (blood pressure) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Blood trace element (Cu levels) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Blood trace element (Cu levels) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

blood protein disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease blood protein disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

blood platelet disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease blood platelet disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

blood coagulation disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease blood coagulation disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

inherited blood coagulation disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease inherited blood coagulation disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

increased blood urea nitrogen (bun) Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the increased blood urea nitrogen (bun) phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood volume homeostasis Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood volume homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of blood circulation Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of blood circulation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

elevated systolic blood pressure Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the elevated systolic blood pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

low-to-normal blood pressure Gene Set

From HPO Gene-Disease Associations

genes associated with the low-to-normal blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased blood urea nitrogen (bun) Gene Set

From HPO Gene-Disease Associations

genes associated with the increased blood urea nitrogen (bun) phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

blood group antigen abnormality Gene Set

From HPO Gene-Disease Associations

genes associated with the blood group antigen abnormality phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated diastolic blood pressure Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated diastolic blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

absent microvilli on the surface of peripheral blood lymphocytes Gene Set

From HPO Gene-Disease Associations

genes associated with the absent microvilli on the surface of peripheral blood lymphocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal concentration of calcium in blood Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal concentration of calcium in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

elevated systolic blood pressure Gene Set

From HPO Gene-Disease Associations

genes associated with the elevated systolic blood pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

prolonged whole-blood clotting time Gene Set

From HPO Gene-Disease Associations

genes associated with the prolonged whole-blood clotting time phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

prominent superficial blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the prominent superficial blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal levels of creatine kinase in blood Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal levels of creatine kinase in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormal umbilical cord blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormal umbilical cord blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased red blood cell mass Gene Set

From HPO Gene-Disease Associations

genes associated with the increased red blood cell mass phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

attenuation of retinal blood vessels Gene Set

From HPO Gene-Disease Associations

genes associated with the attenuation of retinal blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of blood circulation Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of blood circulation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Blood Loss, Surgical Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Loss, Surgical phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood Coagulation Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Coagulation Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood Platelet Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Platelet Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood Coagulation Disorders, Inherited Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Coagulation Disorders, Inherited phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood Group Incompatibility Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Blood Group Incompatibility phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Blood group Rhesus C/E/D polypeptide Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Blood group Rhesus C/E/D polypeptide protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Blood coagulation inhibitor, Disintegrin Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Blood coagulation inhibitor, Disintegrin protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Kell blood group glycoprotein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Kell blood group glycoprotein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal blood gas level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood gas level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased blood urea nitrogen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood cell physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent visceral yolk sac blood islands Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent visceral yolk sac blood islands phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney venous blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney venous blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel endothelium morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel endothelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal systemic arterial blood pressure regulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal systemic arterial blood pressure regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood-brain barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood-brain barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased systemic arterial systolic blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased systemic arterial systolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased blood uric acid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel elastic tissue morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel elastic tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood osmolality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood ph regulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood ph regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood-inner ear barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood-inner ear barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood flow velocity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood flow velocity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mean systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mean systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased systemic arterial diastolic blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased systemic arterial diastolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood urea nitrogen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood coagulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood coagulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood circulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood circulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased mean systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased mean systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal kidney arterial blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal kidney arterial blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased blood urea nitrogen level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased blood urea nitrogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood cell morphology/development Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood cell morphology/development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood uric acid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood homeostasis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal umbilical cord blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal umbilical cord blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal placenta fetal blood space morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal placenta fetal blood space morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal retinal blood vessel pattern Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal retinal blood vessel pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

absent vitelline blood vessels Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the absent vitelline blood vessels phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel physiology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased systemic arterial systolic blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased systemic arterial systolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood-cerebrospinal fluid barrier function Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood-cerebrospinal fluid barrier function phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal urinary bladder blood vessel morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal urinary bladder blood vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal red blood cell deformability Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal red blood cell deformability phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood volume Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal visceral yolk sac blood island morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal visceral yolk sac blood island morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased blood osmolality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased blood osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased red blood cell distribution width Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased red blood cell distribution width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased blood osmolality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased blood osmolality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal blood pressure regulation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal blood pressure regulation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased systemic arterial diastolic blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased systemic arterial diastolic blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal circadian regulation of systemic arterial blood pressure Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal circadian regulation of systemic arterial blood pressure phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased blood uric acid level Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased blood uric acid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

[blood group, swann] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, swann] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, rodgers] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, rodgers] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, colton] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, colton] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, knops system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, knops system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[junior blood group system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [junior blood group system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, raph] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, raph] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group gil] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group gil] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, dombrock] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, dombrock] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, waldner] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, waldner] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, scianna system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, scianna system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, mn] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, mn] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, xg system] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [blood group, xg system] phenotype from the curated OMIM Gene-Disease Associations dataset.

[blood group, lutheran system] Gene Set