Name

GAD High Level Gene-Disease Associations Dataset

From Genetic Association Database

gene-disease associations curated from genetic association studies

dbGAP Gene-Trait Associations Dataset

From Database of Genotypes and Phenotypes

gene-trait associations curated from genetic association studies

RNU6-46P Gene

RNA, U6 small nuclear 46, pseudogene

RNU7-47P Gene

RNA, U7 small nuclear 47 pseudogene

RNU6-48P Gene

RNA, U6 small nuclear 48, pseudogene

RNU7-42P Gene

RNA, U7 small nuclear 42 pseudogene

IGHV3-43D Gene

immunoglobulin heavy variable 3-43D

RNU7-41P Gene

RNA, U7 small nuclear 41 pseudogene

RNU6-45P Gene

RNA, U6 small nuclear 45, pseudogene

RNU7-49P Gene

RNA, U7 small nuclear 49 pseudogene

RNU7-44P Gene

RNA, U7 small nuclear 44 pseudogene

RNU7-43P Gene

RNA, U7 small nuclear 43 pseudogene

CTC-436P18.1 Gene

uncharacterized LOC101928630

CTB-49A3.2 Gene

uncharacterized LOC105379181

RNU7-46P Gene

RNA, U7 small nuclear 46 pseudogene

RNU7-40P Gene

RNA, U7 small nuclear 40 pseudogene

CH507-42P11.6 Gene

putative uncharacterized protein C21orf125

CTB-41I6.1 Gene

uncharacterized LOC101928235

RNU7-45P Gene

RNA, U7 small nuclear 45 pseudogene

CH17-408M7.1 Gene

uncharacterized LOC102724558

RNU7-48P Gene

RNA, U7 small nuclear 48 pseudogene

RNU6-42P Gene

RNA, U6 small nuclear 42, pseudogene

HDLCQ6 Gene

High density lipoprotein cholesterol level QTL 6

HDLCQ1 Gene

high density lipoprotein cholesterol level QTL 1

HDLCQ4 Gene

High density lipoprotein cholesterol level QTL 4

HDLCQ5 Gene

High density lipoprotein cholesterol level QTL 5

HDLCQ2 Gene

High density lipoprotein cholesterol level QTL on chromosome 8

HDLC3 Gene

High density lipoprotein cholesterol, low serum, 3

HCHGQ1 Gene

Hematocrit/hemoglobin quantitative trait locus 1

HCHGQ3 Gene

Hematocrit/hemoglobin quantitative trait locus 3

HCHGQ2 Gene

Hematocrit/hemoglobin quantitative trait locus 2

BMIQ8 Gene

body mass index quantitative trait locus 8

HPCQTL19 Gene

Prostate cancer aggressiveness quantitative trait locus on chromosome 19

STQTL8 Gene

stature quantitative trait locus 8

STQTL4 Gene

stature quantitative trait locus 4

STQTL5 Gene

stature quantitative trait locus 5

STQTL2 Gene

stature quantitative trait locus 2

STQTL3 Gene

stature quantitative trait locus 3

STQTL6 Gene

stature quantitative trait locus 6

STQTL7 Gene

stature quantitative trait locus 7

MUSTQTL1 Gene

Muscle strength quantitative trait locus 1

SQTL2 Gene

Smoking as a quantitative trait locus 2

BSZQTL3 Gene

Bone size quantitative trait locus 3

SQTL1 Gene

Smoking as a quantitative trait locus 1

GEVQ1 Gene

gene expression, variation in, quantitative trait locus

GEVQ2 Gene

gene expression, variation in, quantitative trait locus

BMND8 Gene

bone mineral density quantiative trait locus 8

BMND7 Gene

bone mineral density quantiative trait locus 7

HDLBP Gene

high density lipoprotein binding protein

The protein encoded by this gene binds high density lipoprotein (HDL) and may function to regulate excess cholesterol levels in cells. The encoded protein also binds RNA and can induce heterochromatin formation. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]

GPIHBP1 Gene

glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1

This gene encodes a capillary endothelial cell protein that facilitates the lipolytic processing of triglyceride-rich lipoproteins. The encoded protein is a glycosylphosphatidylinositol-anchored protein that is a member of the lymphocyte antigen 6 (Ly6) family. This protein plays a major role in transporting lipoprotein lipase (LPL) from the subendothelial spaces to the capillary lumen. Mutations in this gene are the cause of hyperlipoproteinemia, type 1D. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Sep 2014]

LOC100421281 Gene

high density lipoprotein binding protein pseudogene

CLQTL2 Gene

Cholesterol level QTL 2

LDLRAD1 Gene

low density lipoprotein receptor class A domain containing 1

LDLRAD2 Gene

low density lipoprotein receptor class A domain containing 2

LDLRAD3 Gene

low density lipoprotein receptor class A domain containing 3

LRP2 Gene

low density lipoprotein receptor-related protein 2

The protein encoded by this gene, low density lipoprotein-related protein 2 (LRP2) or megalin, is a multi-ligand endocytic receptor that is expressed in many different tissues but primarily in absorptive epithilial tissues such as the kidney. This glycoprotein has a large amino-terminal extracellular domain, a single transmembrane domain, and a short carboxy-terminal cytoplasmic tail. The extracellular ligand-binding-domains bind diverse macromolecules including albumin, apolipoproteins B and E, and lipoprotein lipase. The LRP2 protein is critical for the reuptake of numerous ligands, including lipoproteins, sterols, vitamin-binding proteins, and hormones. This protein also has a role in cell-signaling; extracellular ligands include parathyroid horomones and the morphogen sonic hedgehog while cytosolic ligands include MAP kinase scaffold proteins and JNK interacting proteins. Recycling of this membrane receptor is regulated by phosphorylation of its cytoplasmic domain. Mutations in this gene cause Donnai-Barrow syndrome (DBS) and facio-oculoacoustico-renal syndrome (FOAR).[provided by RefSeq, Aug 2009]

LRP3 Gene

low density lipoprotein receptor-related protein 3

LRP1 Gene

low density lipoprotein receptor-related protein 1

The protein encoded by this gene is an endocytic receptor involved in several cellular processes, including intracellular signaling, lipid homeostasis, and clearance of apoptotic cells. In addition, the encoded protein is necessary for the A2M-mediated clearance of secreted amyloid precursor protein and beta-amyloid, the main component of amyloid plaques found in Alzheimer patients. Expression of this gene decreases with age and has been found to be lower than controls in brain tissue from Alzheimer patients. [provided by RefSeq, Jan 2010]

LRP6 Gene

low density lipoprotein receptor-related protein 6

This gene encodes a member of the low density lipoprotein (LDL) receptor gene family. LDL receptors are transmembrane cell surface proteins involved in receptor-mediated endocytosis of lipoprotein and protein ligands. The protein encoded by this gene functions as a receptor or, with Frizzled, a co-receptor for Wnt and thereby transmits the canonical Wnt/beta-catenin signaling cascade. Through its interaction with the Wnt/beta-catenin signaling cascade this gene plays a role in the regulation of cell differentiation, proliferation, and migration and the development of many cancer types. This protein undergoes gamma-secretase dependent RIP- (regulated intramembrane proteolysis) processing but the precise locations of the cleavage sites have not been determined.[provided by RefSeq, Dec 2009]

LRP4 Gene

low density lipoprotein receptor-related protein 4

This gene encodes a member of the low-density lipoprotein receptor-related protein family. The encoded protein may be a regulator of Wnt signaling. Mutations in this gene are associated with Cenani-Lenz syndrome. [provided by RefSeq, May 2010]

LRP5 Gene

low density lipoprotein receptor-related protein 5

This gene encodes a transmembrane low-density lipoprotein receptor that binds and internalizes ligands in the process of receptor-mediated endocytosis. This protein also acts as a co-receptor with Frizzled protein family members for transducing signals by Wnt proteins and was originally cloned on the basis of its association with type 1 diabetes mellitus in humans. This protein plays a key role in skeletal homeostasis and many bone density related diseases are caused by mutations in this gene. Mutations in this gene also cause familial exudative vitreoretinopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2014]

LRP8 Gene

low density lipoprotein receptor-related protein 8, apolipoprotein e receptor

This gene encodes a member of the low density lipoprotein receptor (LDLR) family. Low density lipoprotein receptors are cell surface proteins that play roles in both signal transduction and receptor-mediated endocytosis of specific ligands for lysosomal degradation. The encoded protein plays a critical role in the migration of neurons during development by mediating Reelin signaling, and also functions as a receptor for the cholesterol transport protein apolipoprotein E. Expression of this gene may be a marker for major depressive disorder. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Jun 2011]

LRPAP1 Gene

low density lipoprotein receptor-related protein associated protein 1

This gene encodes a protein that interacts with the low density lipoprotein (LDL) receptor-related protein and facilitates its proper folding and localization by preventing the binding of ligands. Mutations in this gene have been identified in individuals with myopia 23. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]

OLR1 Gene

oxidized low density lipoprotein (lectin-like) receptor 1

This gene encodes a low density lipoprotein receptor that belongs to the C-type lectin superfamily. This gene is regulated through the cyclic AMP signaling pathway. The encoded protein binds, internalizes and degrades oxidized low-density lipoprotein. This protein may be involved in the regulation of Fas-induced apoptosis. This protein may play a role as a scavenger receptor. Mutations of this gene have been associated with atherosclerosis, risk of myocardial infarction, and may modify the risk of Alzheimer's disease. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Feb 2010]

LDLR Gene

low density lipoprotein receptor

The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. Low density lipoprotein (LDL) is normally bound at the cell membrane and taken into the cell ending up in lysosomes where the protein is degraded and the cholesterol is made available for repression of microsomal enzyme 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase, the rate-limiting step in cholesterol synthesis. At the same time, a reciprocal stimulation of cholesterol ester synthesis takes place. Mutations in this gene cause the autosomal dominant disorder, familial hypercholesterolemia. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Sep 2010]

LRP5L Gene

low density lipoprotein receptor-related protein 5-like

LDLRAD4 Gene

low density lipoprotein receptor class A domain containing 4

VLDLR Gene

very low density lipoprotein receptor

The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. This gene encodes a lipoprotein receptor that is a member of the LDLR family and plays important roles in VLDL-triglyceride metabolism and the reelin signaling pathway. Mutations in this gene cause VLDLR-associated cerebellar hypoplasia. Alternative splicing generates multiple transcript variants encoding distinct isoforms for this gene. [provided by RefSeq, Aug 2009]

LOC100421006 Gene

very low density lipoprotein receptor pseudogene

LDLRAP1 Gene

low density lipoprotein receptor adaptor protein 1

The protein encoded by this gene is a cytosolic protein which contains a phosphotyrosine binding (PTD) domain. The PTD domain has been found to interact with the cytoplasmic tail of the LDL receptor. Mutations in this gene lead to LDL receptor malfunction and cause the disorder autosomal recessive hypercholesterolaemia. [provided by RefSeq, Jul 2008]

LRP1B Gene

low density lipoprotein receptor-related protein 1B

LRP1B belongs to the low density lipoprotein (LDL) receptor gene family. These receptors play a wide variety of roles in normal cell function and development due to their interactions with multiple ligands (Liu et al., 2001 [PubMed 11384978]).[supplied by OMIM, Mar 2008]

LRP10 Gene

low density lipoprotein receptor-related protein 10

LRP11 Gene

low density lipoprotein receptor-related protein 11

LRP12 Gene

low density lipoprotein receptor-related protein 12

This gene encodes a member of the low-density lipoprotein receptor related protein family. The product of this gene is a transmembrane protein that is differentially expressed in many cancer cells. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]

CH25H Gene

cholesterol 25-hydroxylase

This is an intronless gene that is involved in cholesterol and lipid metabolism. The encoded protein is a membrane protein and contains clusters of histidine residues essential for catalytic activity. Unlike most other sterol hydroxylases, this enzyme is a member of a small family of enzymes that utilize diiron cofactors to catalyze the hydroxylation of hydrophobic substrates. [provided by RefSeq, Jul 2008]

CLQTL1 Gene

cholesterol-lowering factor

NCEH1 Gene

neutral cholesterol ester hydrolase 1

LIPA Gene

lipase A, lysosomal acid, cholesterol esterase

This gene encodes lipase A, the lysosomal acid lipase (also known as cholesterol ester hydrolase). This enzyme functions in the lysosome to catalyze the hydrolysis of cholesteryl esters and triglycerides. Mutations in this gene can result in Wolman disease and cholesteryl ester storage disease. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2014]

LCAT Gene

lecithin-cholesterol acyltransferase

This gene encodes the extracellular cholesterol esterifying enzyme, lecithin-cholesterol acyltransferase. The esterification of cholesterol is required for cholesterol transport. Mutations in this gene have been found to cause fish-eye disease as well as LCAT deficiency. [provided by RefSeq, Jul 2008]

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

ADIPQTL5 Gene

Adiponectin, serum level of, QTL5

ALPQTL3 Gene

Alkaline phosphatase, plasma level of, QTL3

ALPQTL2 Gene

Alkaline phosphatase, plasma level of, QTL 2

TSHQTL1 Gene

Thyroid-stimulating hormone level QTL 1

ALPQTL4 Gene

Alkaline phosphatase, plasma level of, QTL4

PURAQTL1 Gene

Polyunsaturated fatty acids plasma level QTL1

ADIPQTL4 Gene

Adiponectin, serum level of, QTL4

B6QTL1 Gene

Vitamin B6 plasma level QTL 1

ALPQTL1 Gene

Alkaline phosphatase, plasma level of, QTL1

SXGQTL1 Gene

Sex hormone-binding blobulin circulating level QTL 1

LPAL1 Gene

lipoprotein, Lp(a)-like 1

LPAL2 Gene

lipoprotein, Lp(a)-like 2, pseudogene

Apolipoprotein(a) is the distinguishing protein moiety of lipoprotein(a), of which elevated plasma levels are correlated with an increased risk of atherosclerosis. This gene is similar to the lipoprotein, Lp(a) gene, but all transcripts produced by this gene contain a truncated open reading frame and are candidates for nonsense-mediated decay. Consequently, this gene is considered to be a pseudogene. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]

LSR Gene

lipolysis stimulated lipoprotein receptor

LPL Gene

lipoprotein lipase

LPL encodes lipoprotein lipase, which is expressed in heart, muscle, and adipose tissue. LPL functions as a homodimer, and has the dual functions of triglyceride hydrolase and ligand/bridging factor for receptor-mediated lipoprotein uptake. Severe mutations that cause LPL deficiency result in type I hyperlipoproteinemia, while less extreme mutations in LPL are linked to many disorders of lipoprotein metabolism. [provided by RefSeq, Jul 2008]

LPA Gene

lipoprotein, Lp(a)

The protein encoded by this gene is a serine proteinase that inhibits the activity of tissue-type plasminogen activator I. The encoded protein constitutes a substantial portion of lipoprotein(a) and is proteolytically cleaved, resulting in fragments that attach to atherosclerotic lesions and promote thrombogenesis. Elevated plasma levels of this protein are linked to atherosclerosis. Depending on the individual, the encoded protein contains 2-43 copies of kringle-type domains. The allele represented here contains 15 copies of the kringle-type repeats and corresponds to that found in the reference genome sequence. [provided by RefSeq, Dec 2009]

TFPI Gene

tissue factor pathway inhibitor (lipoprotein-associated coagulation inhibitor)

This gene encodes a protease inhibitor that regulates the tissue factor (TF)-dependent pathway of blood coagulation. The coagulation process initiates with the formation of a factor VIIa-TF complex, which proteolytically activates additional proteases (factors IX and X) and ultimately leads to the formation of a fibrin clot. The product of this gene inhibits the activated factor X and VIIa-TF proteases in an autoregulatory loop. The encoded protein is glycosylated and predominantly found in the vascular endothelium and plasma in both free forms and complexed with plasma lipoproteins. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been confirmed. [provided by RefSeq, Jul 2008]

ATHS Gene

atherosclerosis susceptibility (lipoprotein associated)

LOC729557 Gene

density-regulated protein pseudogene

BMND9 Gene

Bone mineral density QTL 9

BMND6 Gene

Bone mineral density QTL 6

BMND5 Gene

Bone mineral density variation QTL 5

BMND2 Gene

Bone mineral density variation 2

BMND3 Gene

Bone mineral density variability 3

LOC100652897 Gene

density-regulated protein pseudogene

DENR Gene

density-regulated protein

This gene encodes a protein whose expression was found to increase in cultured cells at high density but not during growth arrest. This gene was also shown to have increased expression in cells overexpressing HER-2/neu proto-oncogene. The protein contains an SUI1 domain. In budding yeast, SUI1 is a translation initiation factor that along with eIF-2 and the initiator tRNA-Met, directs the ribosome to the proper translation start site. Proteins similar to SUI have been found in mammals, insects, and plants. [provided by RefSeq, Jul 2008]

BMND10 Gene

Bone mineral density QTL 10

BMND11 Gene

Bone mineral density QTL 11

BMND13 Gene

Bone mineral density QTL 13

BMND14 Gene

Bone mineral density QTL 14

BMND4 Gene

Bone mineral density variation QTL 4

LOC100420064 Gene

density-regulated protein pseudogene

LOC100419923 Gene

density-regulated protein pseudogene

LY6G6C Gene

lymphocyte antigen 6 complex, locus G6C

LY6G6C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]

LY6G6E Gene

lymphocyte antigen 6 complex, locus G6E (pseudogene)

LY6G6E belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]

LY6G6D Gene

lymphocyte antigen 6 complex, locus G6D

LY6G6D belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Apr 2009]

GCOM2 Gene

GRINL1B complex locus 2, pseudogene

GCOM1 Gene

GRINL1A complex locus 1

This locus represents naturally occurring readthrough transcription between the neighboring MYZAP (myocardial zonula adherens protein) and POLR2M (polymerase (RNA) II (DNA directed) polypeptide M) genes on chromosome 15. Alternative splicing results in multiple readthrough transcript variants. Readthrough variants may encode proteins that share sequence identity with the upstream gene product or with both the upstream and downstream gene products. Some readthrough transcript variants are also expected to be candidates for nonsense-mediated decay (NMD). [provided by RefSeq, Oct 2013]

MECOM Gene

MDS1 and EVI1 complex locus

The protein encoded by this gene is a transcriptional regulator and oncoprotein that may be involved in hematopoiesis, apoptosis, development, and cell differentiation and proliferation. The encoded protein can interact with CTBP1, SMAD3, CREBBP, KAT2B, MAPK8, and MAPK9. This gene can undergo translocation with the AML1 gene, resulting in overexpression of this gene and the onset of leukemia. Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Mar 2011]

NPAT Gene

nuclear protein, ataxia-telangiectasia locus

LCR-OPSIN Gene

opsin locus control region

The genes encoding the red (OPN1LW; MIM 300822) and green (OPN1MW; MIM 300821) photopigments are arranged in a head-to-tail tandem array on chromosome Xq28, with a single red pigment gene followed by 1 or more green pigment genes. A master switch for the genes of this locus, called the locus control region (LCR), is located between 3.1 kb and 3.7 kb 5-prime of the gene array and has been shown to be essential for expression of both the red and green pigment genes as well as cone-specific expression of the genes and their segregated expression in separate cones (summary by Deeb, 2005 [PubMed 15811001]).[supplied by OMIM, Mar 2011]

HBN1 Gene

Progressive familial heart block, type I, locus 1

LY6G5C Gene

lymphocyte antigen 6 complex, locus G5C

LY6G5C belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]

LY6G5B Gene

lymphocyte antigen 6 complex, locus G5B

LY6G5B belongs to a cluster of leukocyte antigen-6 (LY6) genes located in the major histocompatibility complex (MHC) class III region on chromosome 6. Members of the LY6 superfamily typically contain 70 to 80 amino acids, including 8 to 10 cysteines. Most LY6 proteins are attached to the cell surface by a glycosylphosphatidylinositol (GPI) anchor that is directly involved in signal transduction (Mallya et al., 2002 [PubMed 12079290]).[supplied by OMIM, Mar 2008]

FLJ32742 Gene

uncharacterized locus FLJ32742

SPEG Gene

SPEG complex locus

This gene encodes a protein with similarity to members of the myosin light chain kinase family. This protein family is required for myocyte cytoskeletal development. Studies in mouse have determined that a lack of this protein affected myocardial development. Multiple alternatively spliced transcript variants have been reported for this gene, but the full-length nature of only two variants that encode different protein isoforms has been defined. [provided by RefSeq, Mar 2010]

GNAS Gene

GNAS complex locus

This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Some transcripts contain a differentially methylated region (DMR) at their 5' exons, and this DMR is commonly found in imprinted genes and correlates with transcript expression. An antisense transcript is produced from an overlapping locus on the opposite strand. One of the transcripts produced from this locus, and the antisense transcript, are paternally expressed noncoding RNAs, and may regulate imprinting in this region. In addition, one of the transcripts contains a second overlapping ORF, which encodes a structurally unrelated protein - Alex. Alternative splicing of downstream exons is also observed, which results in different forms of the stimulatory G-protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors. [provided by RefSeq, Aug 2012]

TRG-AS1 Gene

T cell receptor gamma locus antisense RNA 1

LY6G6F Gene

lymphocyte antigen 6 complex, locus G6F

The human G6f protein is a type I transmembrane protein belonging to the immunoglobin (Ig) superfamily, which is comprised of cell-surface proteins involved in the immune system and cellular recognition (de Vet et al., 2003 [PubMed 12852788]).[supplied by OMIM, Mar 2008]

LCRB Gene

locus control region, beta

UGT1A Gene

UDP glucuronosyltransferase 1 family, polypeptide A complex locus

This RefSeq represents a complex locus that encodes several UDP-glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N-termini and identical C-termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. [provided by RefSeq, Jul 2008]

LOC100289568 Gene

UDP glucuronosyltransferase 2 family, polypeptide A1, complex locus pseudogene

LOC388221 Gene

NPIP-like locus

SCZD11 Gene

Schizophrenia susceptibility locus, chromosome 10q-related

TRA Gene

T cell receptor alpha locus

TRB Gene

T cell receptor beta locus

T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor beta locus. The beta locus includes V (variable), J (joining), diversity (D), and C (constant) segments. During T cell development, the beta chain is synthesized by a recombination event at the DNA level joining a D segment with a J segment; a V segment is then joined to the D-J gene. The C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase. Several V segments and one J segment of the beta locus are known to be incapable of encoding a protein and are considered pseudogenes. The beta locus also includes eight trypsinogen genes, three of which encode functional proteins and five of which are pseudogenes. Chromosomal abnormalities involving the T-cell receptor beta locus have been associated with T-cell lymphomas. [provided by RefSeq, Jul 2008]

TRD Gene

T cell receptor delta locus

TRG Gene

T cell receptor gamma locus

T cell receptors recognize foreign antigens which have been processed as small peptides and bound to major histocompatibility complex (MHC) molecules at the surface of antigen presenting cells (APC). Each T cell receptor is a dimer consisting of one alpha and one beta chain or one delta and one gamma chain. In a single cell, the T cell receptor loci are rearranged and expressed in the order delta, gamma, beta, and alpha. If both delta and gamma rearrangements produce functional chains, the cell expresses delta and gamma. If not, the cell proceeds to rearrange the beta and alpha loci. This region represents the germline organization of the T cell receptor gamma locus. The gamma locus includes V (variable), J (joining), and C (constant) segments. During T cell development, the gamma chain is synthesized by a recombination event at the DNA level joining a V segment with a J segment; the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random addition of nucleotides by terminal deoxynucleotidyltransferase. Several V segments of the gamma locus are known to be incapable of encoding a protein and are considered pseudogenes. Somatic rearrangement of the gamma locus has been observed in T cells derived from patients with T cell leukemia and ataxia telangiectasia. [provided by RefSeq, Jul 2008]

ESP33 Gene

uncharacterized locus ESP33

BDA1B Gene

Brachydactyly, type A1, locus B

DEFA1A3 Gene

defensin, alpha 1 and alpha 3, variable copy number locus

PCDHA@ Gene

protocadherin alpha cluster, complex locus

The protocadherin alpha gene cluster is one of three related clusters tandemly linked on chromosome five. The clusters have a genomic organization similar to that of B-cell and T-cell receptor gene clusters. The alpha gene cluster is composed of 15 genes and 1 pseudogene, which are members of the cadherin superfamily and related to the mouse CNR genes. The sequence of the 13 upstream genes and the pseudogene are highly similar to one another, while a subfamily (C) contains two more distantly related coding sequences. The alpha cluster genes are organized in a tandem array of 15 large, variable region exons followed by a constant region, which contains 3 exons shared by all genes in the cluster. Each variable region exon encodes an extracellular domain comprised of 6 cadherin ectodomains and a transmembrane region. The constant region exons encode a common cytoplasmic tail. These neural adhesion proteins most likely play a critical role in the establishment and function of specific cell-cell connections in the brain. Alternative splicing has been described for the alpha cluster genes. [provided by RefSeq, Jul 2008]

ITS Gene

Insulinoma tumor suppressor gene locus

BGLT3 Gene

beta globin locus transcript 3 (non-protein coding)

STIL Gene

SCL/TAL1 interrupting locus

This gene encodes a cytoplasmic protein implicated in regulation of the mitotic spindle checkpoint, a regulatory pathway that monitors chromosome segregation during cell division to ensure the proper distribution of chromosomes to daughter cells. The protein is phosphorylated in mitosis and in response to activation of the spindle checkpoint, and disappears when cells transition to G1 phase. It interacts with a mitotic regulator, and its expression is required to efficiently activate the spindle checkpoint. It is proposed to regulate Cdc2 kinase activity during spindle checkpoint arrest. Chromosomal deletions that fuse this gene and the adjacent locus commonly occur in T cell leukemias, and are thought to arise through illegitimate V-(D)-J recombination events. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

UGT2A1 Gene

UDP glucuronosyltransferase 2 family, polypeptide A1, complex locus

The protein encoded by this gene belongs to the UDP-glycosyltransferase family, members of which catalyze biotransformation reactions in which lipophilic substrates are conjugated with glucuronic acid to increase water solubility and enhance excretion. They are of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds. This enzyme is expressed in the olfactory neuroepithelium, which lines the posterior nasal cavity and is exposed to a wide range of odorants and airborne toxic compounds. Hence, this protein has been suggested to be involved in clearing lipophilic odorant molecules from the sensory epithelium. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. This gene shares exon structure with the UDP glucuronosyltransferase 2A2 family member, which encodes N-terminally distinct isoforms. [provided by RefSeq, Jul 2014]

LY6E Gene

lymphocyte antigen 6 complex, locus E

LY6D Gene

lymphocyte antigen 6 complex, locus D

LY6K Gene

lymphocyte antigen 6 complex, locus K

LY6H Gene

lymphocyte antigen 6 complex, locus H

IGL Gene

immunoglobulin lambda locus

Immunoglobulins recognize foreign antigens and initiate immune responses such as phagocytosis and the complement system. Each immunoglobulin molecule consists of two identical heavy chains and two identical light chains. There are two classes of light chains, kappa and lambda. This region represents the germline organization of the lambda light chain locus. The locus includes V (variable), J (joining), and C (constant) segments. During B cell development, a recombination event at the DNA level joins a single V segment with a J segment; the C segment is later joined by splicing at the RNA level. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase, and by somatic hypermutation, which occurs during B cell maturation in the spleen and lymph nodes. Several V segments and three C segments are known to be incapable of encoding a protein and are considered pseudogenes. The locus also includes several non-immunoglobulin genes, many of which are pseudogenes or are predicted by automated computational analysis or homology to other species. [provided by RefSeq, Jul 2008]

IGK Gene

immunoglobulin kappa locus

IGH Gene

immunoglobulin heavy locus

Immunoglobulins recognize foreign antigens and initiate immune responses such as phagocytosis and the complement system. Each immunoglobulin molecule consists of two identical heavy chains and two identical light chains. This region represents the germline organization of the heavy chain locus. The locus includes V (variable), D (diversity), J (joining), and C (constant) segments. During B cell development, a recombination event at the DNA level joins a single D segment with a J segment; this partially rearranged D-J gene is then joined to a V segment. The rearranged V-D-J is then transcribed with the IGHM constant region; this transcript encodes a mu heavy chain. Later in development B cells generate V-D-J-Cmu-Cdelta pre-messenger RNA, which is alternatively spliced to encode either a mu or a delta heavy chain. Mature B cells in the lymph nodes undergo switch recombination, so that the V-D-J gene is brought in proximity to one of the IGHG, IGHA, or IGHE genes and each cell expresses either the gamma, alpha, or epsilon heavy chain. Recombination of many different V segments with several J segments provides a wide range of antigen recognition. Additional diversity is attained by junctional diversity, resulting from the random additional of nucleotides by terminal deoxynucleotidyltransferase, and by somatic hypermutation, which occurs during B cell maturation in the spleen and lymph nodes. Due to polymorphism, the numbers of functional V, J, and D genes differ among individuals and some V, D, J, and C segments may be pseudogenes. [provided by RefSeq, Oct 2013]

HMGN2P31 Gene

high mobility group nucleosomal binding domain 2 pseudogene 31

HMGB3P5 Gene

high mobility group box 3 pseudogene 5

HMGN2P19 Gene

high mobility group nucleosomal binding domain 2 pseudogene 19

HMGN2P18 Gene

high mobility group nucleosomal binding domain 2 pseudogene 18

HMGN2P12 Gene

high mobility group nucleosomal binding domain 2 pseudogene 12

HMGN2P11 Gene

high mobility group nucleosomal binding domain 2 pseudogene 11

HMGN2P10 Gene

high mobility group nucleosomal binding domain 2 pseudogene10

HMGN2P17 Gene

high mobility group nucleosomal binding domain 2 pseudogene 17

HMGN2P16 Gene

high mobility group nucleosomal binding domain 2 pseudogene 16

HMGN2P15 Gene

high mobility group nucleosomal binding domain 2 pseudogene 15

HMGN2P14 Gene

high mobility group nucleosomal binding domain 2 pseudogene14

FCER1G Gene

Fc fragment of IgE, high affinity I, receptor for; gamma polypeptide

The high affinity IgE receptor is a key molecule involved in allergic reactions. It is a tetramer composed of 1 alpha, 1 beta, and 2 gamma chains. The gamma chains are also subunits of other Fc receptors. [provided by RefSeq, Jul 2008]

FCER1A Gene

Fc fragment of IgE, high affinity I, receptor for; alpha polypeptide

The immunoglobulin epsilon receptor (IgE receptor) is the initiator of the allergic response. When two or more high-affinity IgE receptors are brought together by allergen-bound IgE molecules, mediators such as histamine that are responsible for allergy symptoms are released. This receptor is comprised of an alpha subunit, a beta subunit, and two gamma subunits. The protein encoded by this gene represents the alpha subunit. [provided by RefSeq, Aug 2011]

HMGN1P9 Gene

high mobility group nucleosome binding domain 1 pseudogene

HMGN1P4 Gene

high mobility group nucleosome binding domain 1 pseudogene 4

HMGN1P5 Gene

high mobility group nucleosome binding domain 1 pseudogene 5

HMGN1P6 Gene

high mobility group nucleosome binding domain 1 pseudogene 6

HMGN1P7 Gene

high mobility group nucleosome binding domain 1 pseudogene 7

HMGN1P1 Gene

high mobility group nucleosome binding domain 1 pseudogene 1

HMGN1P2 Gene

high mobility group nucleosome binding domain 1 pseudogene 2

LOC100129956 Gene

high mobility group nucleosomal binding domain 2 pseudogene

HMGB3 Gene

high mobility group box 3

This gene encodes a member of a family of proteins containing one or more high mobility group DNA-binding motifs. The encoded protein plays an important role in maintaining stem cell populations, and may be aberrantly expressed in tumor cells. A mutation in this gene was associated with microphthalmia, syndromic 13. There are numerous pseudogenes of this gene on multiple chromosomes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]

HMGB4 Gene

high mobility group box 4

HMGN2P13 Gene

high mobility group nucleosomal binding domain 2 pseudogene 13

HMGB1P12 Gene

high mobility group box 1 pseudogene 12

HMGB1P10 Gene

high mobility group box 1 pseudogene 10

HMGB1P16 Gene

high mobility group box 1 pseudogene 16

HMGB1P17 Gene

high mobility group box 1 pseudogene 17

HMGB1P36 Gene

high mobility group box 1 pseudogene 36

HMGB3P22 Gene

high mobility group box 3 pseudogene 22

MYP18 Gene

myopia 18 (high grade, autosomal recessive)

This locus was identified by linkage in one consanguineous Chinese family to lie between D14S984 and D14S999. [provided by RefSeq, Feb 2010]

MYP11 Gene

myopia 11 (high grade, autosomal dominant)

HMGN1P8 Gene

high mobility group nucleosome binding domain 1 pseudogene 8

HMGN1P3 Gene

high mobility group nucleosome binding domain 1 pseudogene 3

HMGB1P1 Gene

high mobility group box 1 pseudogene 1

This gene may represent an evolving retropseudogene of the high-mobility group box 1 gene, which has multiple pseudogenes. This gene has an intact open reading frame, where the length of encoded protein is conserved, compared to the high-mobility group box 1 protein. However, due to the lack of conclusive evidence for specific transcription at this location, this locus is currently represented as a pseudogene. [provided by RefSeq, Jan 2010]

HMGB1P3 Gene

high mobility group box 1 pseudogene 3

HMGB1P4 Gene

high mobility group box 1 pseudogene 4

HMGB1P5 Gene

high mobility group box 1 pseudogene 5

HMGN1P16 Gene

high mobility group nucleosome binding domain 1 pseudogene 16

HMGN1P17 Gene

high mobility group nucleosome binding domain 1 pseudogene 17

HMGN1P13 Gene

high mobility group nucleosome binding domain 1 pseudogene 13

HMGN1P10 Gene

high mobility group nucleosome binding domain 1 pseudogene 10

HMGN1P11 Gene

high mobility group nucleosome binding domain 1 pseudogene 11

HMGN1P33 Gene

high mobility group nucleosome binding domain 1 pseudogene 33

HMGN1P34 Gene

high mobility group nucleosome binding domain 1 pseudogene 34

HMGB3P32 Gene

high mobility group box 3 pseudogene 32

HMGB3P30 Gene

high mobility group box 3 pseudogene 30

HMGB3P31 Gene

high mobility group box 3 pseudogene 31

HMGN2P33 Gene

high mobility group nucleosomal binding domain 2 pseudogene 33

HMGN2P32 Gene

high mobility group nucleosomal binding domain 2 pseudogene 32

HMGN2P35 Gene

high mobility group nucleosomal binding domain 2 pseudogene 35

HMGN2P34 Gene

high mobility group nucleosomal binding domain 2 pseudogene 34

HMGN2P37 Gene

high mobility group nucleosomal binding domain 2 pseudogene 37

HMGN2P36 Gene

high mobility group nucleosomal binding domain 2 pseudogene 36

HMGN2P39 Gene

high mobility group nucleosomal binding domain 2 pseudogene 39

HMGN2P38 Gene

high mobility group nucleosomal binding domain 2 pseudogene 38

HMGB1P27 Gene

high mobility group box 1 pseudogene 27

HMGB1P24 Gene

high mobility group box 1 pseudogene 24

HMGB1P22 Gene

high mobility group box 1 pseudogene 22

HMGB1P29 Gene

high mobility group box 1 pseudogene 29

NTSR1 Gene

neurotensin receptor 1 (high affinity)

Neurotensin receptor 1 belongs to the large superfamily of G-protein coupled receptors. NTSR1 mediates the multiple functions of neurotensin, such as hypotension, hyperglycemia, hypothermia, antinociception, and regulation of intestinal motility and secretion. [provided by RefSeq, Jul 2008]

HMGB1P18 Gene

high mobility group box 1 pseudogene 18

HMGB1P19 Gene

high mobility group box 1 pseudogene 19

HMGB1P11 Gene

high mobility group box 1 pseudogene 11

HMGB1P14 Gene

high mobility group box 1 pseudogene 14

HMGB1P15 Gene

high mobility group box 1 pseudogene 15

HMGB2 Gene

high mobility group box 2

This gene encodes a member of the non-histone chromosomal high mobility group protein family. The proteins of this family are chromatin-associated and ubiquitously distributed in the nucleus of higher eukaryotic cells. In vitro studies have demonstrated that this protein is able to efficiently bend DNA and form DNA circles. These studies suggest a role in facilitating cooperative interactions between cis-acting proteins by promoting DNA flexibility. This protein was also reported to be involved in the final ligation step in DNA end-joining processes of DNA double-strand breaks repair and V(D)J recombination. [provided by RefSeq, Jul 2008]

HMGB1 Gene

high mobility group box 1

HMGN3P1 Gene

high mobility group nucleosomal binding domain 3 pseudogene 1

HMGB1P45 Gene

high mobility group box 1 pseudogene 45

HMGA2 Gene

high mobility group AT-hook 2

This gene encodes a protein that belongs to the non-histone chromosomal high mobility group (HMG) protein family. HMG proteins function as architectural factors and are essential components of the enhancesome. This protein contains structural DNA-binding domains and may act as a transcriptional regulating factor. Identification of the deletion, amplification, and rearrangement of this gene that are associated with myxoid liposarcoma suggests a role in adipogenesis and mesenchymal differentiation. A gene knock out study of the mouse counterpart demonstrated that this gene is involved in diet-induced obesity. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]

HMGB1P41 Gene

high mobility group box 1 pseudogene 41

HMGB1P40 Gene

high mobility group box 1 pseudogene 40

HMGB1P44 Gene

high mobility group box 1 pseudogene 44

HMGB1P47 Gene

high mobility group box 1 pseudogene 47

HMGB1P49 Gene

high mobility group box 1 pseudogene 49

HMGB1P48 Gene

high mobility group box 1 pseudogene 48

HMGN1P23 Gene

high mobility group nucleosome binding domain 1 pseudogene 23

HMGN1P22 Gene

high mobility group nucleosome binding domain 1 pseudogene 22

HMGN1P21 Gene

high mobility group nucleosome binding domain 1 pseudogene 21

HMGN1P27 Gene

high mobility group nucleosome binding domain 1 pseudogene 27

HMGN1P26 Gene

high mobility group nucleosome binding domain 1 pseudogene 26

HMGN1P25 Gene

high mobility group nucleosome binding domain 1 pseudogene 25

HMGN1P24 Gene

high mobility group nucleosome binding domain 1 pseudogene 24

HMGN1P29 Gene

high mobility group nucleosome binding domain 1 pseudogene 29

HMGN1P28 Gene

high mobility group nucleosome binding domain 1 pseudogene 28

HMGB3P2 Gene

high mobility group box 3 pseudogene 2

HMGB3P3 Gene

high mobility group box 3 pseudogene 3

HMGB3P1 Gene

high mobility group box 3 pseudogene 1

HMGB3P6 Gene

high mobility group box 3 pseudogene 6

HMGB3P7 Gene

high mobility group box 3 pseudogene 7

HMGB3P4 Gene

high mobility group box 3 pseudogene 4

HMGB3P8 Gene

high mobility group box 3 pseudogene 8

HMGB3P9 Gene

high mobility group box 3 pseudogene 9

HMG20A Gene

high mobility group 20A

HMG20B Gene

high mobility group 20B

HMGA1P4 Gene

high mobility group AT-hook 1 pseudogene 4

HMGA1P6 Gene

high mobility group AT-hook 1 pseudogene 6

HMGB1P34 Gene

high mobility group box 1 pseudogene 34

HMGB1P37 Gene

high mobility group box 1 pseudogene 37

HMGB1P30 Gene

high mobility group box 1 pseudogene 30

HMGB1P38 Gene

high mobility group box 1 pseudogene 38

HMGB1P39 Gene

high mobility group box 1 pseudogene 39

HMGN1P35 Gene

high mobility group nucleosome binding domain 1 pseudogene 35

HMGB1P35 Gene

high mobility group box 1 pseudogene 35

HMGB1P31 Gene

high mobility group box 1 pseudogene 31

HMGB1P32 Gene

high mobility group box 1 pseudogene 32

HMGN5 Gene

high mobility group nucleosome binding domain 5

This gene encodes a nuclear protein with similarities to the high mobility group proteins, HMG14 and HMG17, which suggests that this protein may function as a nucleosomal binding and transcriptional activating protein. [provided by RefSeq, Sep 2009]

HMGN4 Gene

high mobility group nucleosomal binding domain 4

The protein encoded by this gene, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. [provided by RefSeq, Mar 2013]

HMGN3 Gene

high mobility group nucleosomal binding domain 3

Thyroid hormone receptors are hormone-dependent transcription factors that regulate expression of a variety of specific target genes. The protein encoded by this gene binds thyroid hormone receptor beta, but only in the presence of thyroid hormone. The encoded protein, a member of the HMGN protein family, is thought to reduce the compactness of the chromatin fiber in nucleosomes, thereby enhancing transcription from chromatin templates. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]

HMGN2 Gene

high mobility group nucleosomal binding domain 2

The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMGN1, the encoded protein may help maintain an open chromatin configuration around transcribable genes. The protein has also been found to have antimicrobial activity against bacteria, viruses and fungi. [provided by RefSeq, Oct 2014]

HMGN1 Gene

high mobility group nucleosome binding domain 1

The protein encoded by this gene binds nucleosomal DNA and is associated with transcriptionally active chromatin. Along with a similar protein, HMG17, the encoded protein may help maintain an open chromatin configuration around transcribable genes. [provided by RefSeq, Aug 2011]

HMGA1P8 Gene

high mobility group AT-hook 1 pseudogene 8 (functional)

HMGA1P5 Gene

high mobility group AT-hook 1 pseudogene 5

HMGA1P7 Gene

high mobility group AT-hook 1 pseudogene 7

HMGA1P1 Gene

high mobility group AT-hook 1 pseudogene 1

HMGA1P3 Gene

high mobility group AT-hook 1 pseudogene 3

HMGA1P2 Gene

high mobility group AT-hook 1 pseudogene 2

HMGB1P33 Gene

high mobility group box 1 pseudogene 33

MYP12 Gene

myopia 12 (high grade, autosomal dominant)

HMGA1 Gene

high mobility group AT-hook 1

This gene encodes a non-histone protein involved in many cellular processes, including regulation of inducible gene transcription, integration of retroviruses into chromosomes, and the metastatic progression of cancer cells. The encoded protein preferentially binds to the minor groove of A+T-rich regions in double-stranded DNA. It has little secondary structure in solution but assumes distinct conformations when bound to substrates such as DNA or other proteins. The encoded protein is frequently acetylated and is found in the nucleus. At least seven transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

HMGN2P30 Gene

high mobility group nucleosomal binding domain 2 pseudogene 30

HMGN2P26 Gene

high mobility group nucleosomal binding domain 2 pseudogene 26

HMGN2P27 Gene

high mobility group nucleosomal binding domain 2 pseudogene 27

HMGN2P22 Gene

high mobility group nucleosomal binding domain 2 pseudogene 22

HMGN2P23 Gene

high mobility group nucleosomal binding domain 2 pseudogene 23

HMGN2P20 Gene

high mobility group nucleosomal binding domain 2 pseudogene 20

HMGN2P21 Gene

high mobility group nucleosomal binding domain 2 pseudogene 21

HMGN2P7 Gene

high mobility group nucleosomal binding domain 2 pseudogene 7

HMGN2P6 Gene

high mobility group nucleosomal binding domain 2 pseudogene 6

HMGN2P5 Gene

high mobility group nucleosomal binding domain 2 pseudogene 5

HMGN2P3 Gene

high mobility group nucleosomal binding domain 2 pseudogene 3

HMGN2P2 Gene

high mobility group nucleosomal binding domain 2 pseudogene 2

HMGN2P1 Gene

high mobility group nucleosomal binding domain 2 pseudogene 1

HMGN2P9 Gene

high mobility group nucleosomal binding domain 2 pseudogene 9

HMGB1P26 Gene

high mobility group box 1 pseudogene 26

HMGB1P23 Gene

high mobility group box 1 pseudogene 23

HMGB1P28 Gene

high mobility group box 1 pseudogene 28

HMGB1P8 Gene

high mobility group box 1 pseudogene 8

HMGB1P9 Gene

high mobility group box 1 pseudogene 9

FCGR1C Gene

Fc fragment of IgG, high affinity Ic, receptor (CD64), pseudogene

The gene represents one of three related immunoglobulin gamma Fc receptor genes located on chromosome 1. This family member lacks the transmembrane and coiled-coiled domains found in other family members and is thought to be a pseudogene of Fc-gamma-receptor 1A. [provided by RefSeq, Apr 2009]

FCGR1B Gene

Fc fragment of IgG, high affinity Ib, receptor (CD64)

Three distinct, but closely related classes of receptors that bind the Fc portion of IgG have been identified (Fcgamma RI, II and III). The FcgammaRI family consists of three closely related genes termed A, B, and C. This gene encodes the low affinity FcgammaRIB receptor that may play an important role in humoral immune response. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Oct 2011]

FCGR1A Gene

Fc fragment of IgG, high affinity Ia, receptor (CD64)

This gene encodes a protein that plays an important role in the immune response. This protein is a high-affinity Fc-gamma receptor. The gene is one of three related gene family members located on chromosome 1. [provided by RefSeq, Jul 2008]

HMGN1P14 Gene

high mobility group nucleosome binding domain 1 pseudogene 14

HMGN1P15 Gene

high mobility group nucleosome binding domain 1 pseudogene 15

HMGN1P19 Gene

high mobility group nucleosome binding domain 1 pseudogene 19

HMGB1P25 Gene

high mobility group box 1 pseudogene 25

HMGB1P21 Gene

high mobility group box 1 pseudogene 21

HMGB1P20 Gene

high mobility group box 1 pseudogene 20

HTL Gene

high L-leucine transport

HMGB1P43 Gene

high mobility group box 1 pseudogene 43

HMGB1P42 Gene

high mobility group box 1 pseudogene 42

HMGB1P46 Gene

high mobility group box 1 pseudogene 46

HMGB2P1 Gene

high mobility group box 2 pseudogene 1

HMGN1P18 Gene

high mobility group nucleosome binding domain 1 pseudogene 18

HMGB1P13 Gene

high mobility group box 1 pseudogene 13

HMGB3P25 Gene

high mobility group box 3 pseudogene 25

HMGB3P24 Gene

high mobility group box 3 pseudogene 24

HMGB3P27 Gene

high mobility group box 3 pseudogene 27

HMGB3P26 Gene

high mobility group box 3 pseudogene 26

HMGB3P20 Gene

high mobility group box 3 pseudogene 20

HMGN2P28 Gene

high mobility group nucleosomal binding domain 2 pseudogene 28

HMGN2P29 Gene

high mobility group nucleosomal binding domain 2 pseudogene 29

HMGN2P25 Gene

high mobility group nucleosomal binding domain 2 pseudogene 25

HMGN2P24 Gene

high mobility group nucleosomal binding domain 2 pseudogene 24

HMGN1P30 Gene

high mobility group nucleosome binding domain 1 pseudogene 30

HMGN1P31 Gene

high mobility group nucleosome binding domain 1 pseudogene 31

HMGN1P32 Gene

high mobility group nucleosome binding domain 1 pseudogene 32

HMGN1P36 Gene

high mobility group nucleosome binding domain 1 pseudogene 36

HMGN1P37 Gene

high mobility group nucleosome binding domain 1 pseudogene 37

HMGN1P38 Gene

high mobility group nucleosome binding domain 1 pseudogene 38

TOX Gene

thymocyte selection-associated high mobility group box

The protein encoded by this gene contains a HMG box DNA binding domain. HMG boxes are found in many eukaryotic proteins involved in chromatin assembly, transcription and replication. This protein may function to regulate T-cell development.[provided by RefSeq, Apr 2009]

HMGB1P6 Gene

high mobility group box 1 pseudogene 6

HMGB1P7 Gene

high mobility group box 1 pseudogene 7

HMGN2P44 Gene

high mobility group nucleosomal binding domain 2 pseudogene 44

HMGN2P45 Gene

high mobility group nucleosomal binding domain 2 pseudogene 45

HMGN2P46 Gene

high mobility group nucleosomal binding domain 2 pseudogene 46

HMGN2P40 Gene

high mobility group nucleosomal binding domain 2 pseudogene 40

HMGN2P41 Gene

high mobility group nucleosomal binding domain 2 pseudogene 41

HMGN2P42 Gene

high mobility group nucleosomal binding domain 2 pseudogene 42

HMGN2P43 Gene

high mobility group nucleosomal binding domain 2 pseudogene 43

TOX4 Gene

TOX high mobility group box family member 4

TOX3 Gene

TOX high mobility group box family member 3

The protein encoded by this gene contains an HMG-box, indicating that it may be involved in bending and unwinding of DNA and alteration of chromatin structure. The C-terminus of the encoded protein is glutamine-rich due to CAG repeats in the coding sequence. A minor allele of this gene has been implicated in an elevated risk of breast cancer. Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2009]

TOX2 Gene

TOX high mobility group box family member 2

FCAMR Gene

Fc receptor, IgA, IgM, high affinity

HMGN1P20 Gene

high mobility group nucleosome binding domain 1 pseudogene 20

HMGB3P14 Gene

high mobility group box 3 pseudogene 14

HMGB3P15 Gene

high mobility group box 3 pseudogene 15

HMGB3P16 Gene

high mobility group box 3 pseudogene 16

HMGB3P17 Gene

high mobility group box 3 pseudogene 17

HMGB3P10 Gene

high mobility group box 3 pseudogene 10

HMGB3P11 Gene

high mobility group box 3 pseudogene 11

HMGB3P12 Gene

high mobility group box 3 pseudogene 12

HMGB3P13 Gene

high mobility group box 3 pseudogene 13

HMGB3P18 Gene

high mobility group box 3 pseudogene 18

HMGB3P19 Gene

high mobility group box 3 pseudogene 19

MYP2 Gene

myopia 2 (high grade, autosomal dominant)

MYP3 Gene

myopia 3 (high grade, autosomal dominant)

MYP4 Gene

myopia 4 (high grade, autosomal dominant)

MYP5 Gene

myopia 5 (high grade, autosomal dominant)

HMGB3P29 Gene

high mobility group box 3 pseudogene 29

HMGB3P28 Gene

high mobility group box 3 pseudogene 28

HMGB3P21 Gene

high mobility group box 3 pseudogene 21

HMGB3P23 Gene

high mobility group box 3 pseudogene 23

HMGN2P4 Gene

high mobility group nucleosomal binding domain 2 pseudogene 4

HMGN2P8 Gene

high mobility group nucleosomal binding domain 2 pseudogene 8

SLC1A6 Gene

solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6

SLC1A1 Gene

solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1

This gene encodes a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels. This transporter also transports aspartate, and mutations in this gene are thought to cause dicarboxylicamino aciduria, also known as glutamate-aspartate transport defect. [provided by RefSeq, Mar 2010]

SLC1A2 Gene

solute carrier family 1 (glial high affinity glutamate transporter), member 2

This gene encodes a member of a family of solute transporter proteins. The membrane-bound protein is the principal transporter that clears the excitatory neurotransmitter glutamate from the extracellular space at synapses in the central nervous system. Glutamate clearance is necessary for proper synaptic activation and to prevent neuronal damage from excessive activation of glutamate receptors. Mutations in and decreased expression of this protein are associated with amyotrophic lateral sclerosis. Alternatively spliced transcript variants of this gene have been identified. [provided by RefSeq, Sep 2010]

SLC1A3 Gene

solute carrier family 1 (glial high affinity glutamate transporter), member 3

This gene encodes a member of a member of a high affinity glutamate transporter family. This gene functions in the termination of excitatory neurotransmission in central nervous system. Mutations are associated with episodic ataxia, Type 6. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Feb 2014]

TOX4P1 Gene

TOX high mobility group box family member 4 pseudogene 1

CCHE1 Gene

cervical carcinoma high-expressed lncRNA 1

HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 4 from the curated CTD Gene-Disease Associations dataset.

HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 12 from the curated CTD Gene-Disease Associations dataset.

HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 14 from the curated CTD Gene-Disease Associations dataset.

HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1 from the curated CTD Gene-Disease Associations dataset.

HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 2 from the curated CTD Gene-Disease Associations dataset.

HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 3 from the curated CTD Gene-Disease Associations dataset.

HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 5 from the curated CTD Gene-Disease Associations dataset.

HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HIGH DENSITY LIPOPROTEIN CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 6 from the curated CTD Gene-Disease Associations dataset.

CHOLESTEROL LEVEL QUANTITATIVE TRAIT LOCUS 1 Gene Set

From CTD Gene-Disease Associations

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

BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BONE MINERAL DENSITY QUANTITATIVE TRAIT LOCUS 15 from the curated CTD Gene-Disease Associations dataset.

THYROID-STIMULATING HORMONE LEVEL QUANTITATIVE TRAIT LOCUS 1 Gene Set

From CTD Gene-Disease Associations

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

ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 3 from the curated CTD Gene-Disease Associations dataset.

ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ADIPONECTIN, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS 2 from the curated CTD Gene-Disease Associations 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.

SODIUM SERUM LEVEL QUANTITATIVE TRAIT LOCUS 1 Gene Set

From CTD Gene-Disease Associations

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

VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1 from the curated CTD 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.

high-density lipoprotein cholesterol level. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high-density lipoprotein cholesterol level. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high density lipoprotein cholesterol level Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high density lipoprotein cholesterol level in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl 4] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl 4] phenotype from the curated OMIM Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl 8] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl 8] phenotype from the curated OMIM Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl 12] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl 12] phenotype from the curated OMIM Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl 10] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl 10] phenotype from the curated OMIM Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl 5] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl 5] phenotype from the curated OMIM Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl 9] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl 9] phenotype from the curated OMIM Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl6] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl6] phenotype from the curated OMIM Gene-Disease Associations dataset.

high density lipoprotein cholesterol level qtl14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the high density lipoprotein cholesterol level qtl14 phenotype from the curated OMIM Gene-Disease Associations dataset.

[high density lipoprotein cholesterol level qtl 11] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high density lipoprotein cholesterol level qtl 11] phenotype from the curated OMIM Gene-Disease Associations dataset.

{high density lipoprotein cholesterol level qtl 7} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {high density lipoprotein cholesterol level qtl 7} phenotype from the curated OMIM Gene-Disease Associations dataset.

high plasma concentrations of high density lipoprotein ch Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high plasma concentrations of high density lipoprotein ch in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Fetal hemoglobin quantitative trait locus 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fetal hemoglobin quantitative trait locus 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Fetal hemoglobin quantitative trait locus 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Fetal hemoglobin quantitative trait locus 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 from the curated CTD Gene-Disease Associations dataset.

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9 from the curated CTD Gene-Disease Associations dataset.

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8 from the curated CTD Gene-Disease Associations dataset.

URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 4 from the curated CTD Gene-Disease Associations dataset.

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11 from the curated CTD Gene-Disease Associations dataset.

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13 from the curated CTD Gene-Disease Associations dataset.

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10 from the curated CTD Gene-Disease Associations dataset.

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 from the curated CTD Gene-Disease Associations dataset.

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14 from the curated CTD Gene-Disease Associations dataset.

BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7 from the curated CTD Gene-Disease Associations dataset.

[hematocrit/hemoglobin quantitative trait locus 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [hematocrit/hemoglobin quantitative trait locus 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

[hematocrit/hemoglobin quantitative trait locus 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [hematocrit/hemoglobin quantitative trait locus 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

[hematocrit/hemoglobin quantitative trait locus 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [hematocrit/hemoglobin quantitative trait locus 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone size quantitative trait locus 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone size quantitative trait locus 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

fetal hemoglobin quantitative trait locus 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fetal hemoglobin quantitative trait locus 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

fetal hemoglobin quantitative trait locus 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fetal hemoglobin quantitative trait locus 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

fetal hemoglobin quantitative trait locus 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the fetal hemoglobin quantitative trait locus 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

muscle strength quantitative trait locus 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the muscle strength quantitative trait locus 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

{smoking as a quantitative trait locus 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {smoking as a quantitative trait locus 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{smoking as a quantitative trait locus 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {smoking as a quantitative trait locus 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

[glycerol quantitative trait locus] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [glycerol quantitative trait locus] phenotype from the curated OMIM Gene-Disease Associations dataset.

plasma high density lipoprotein cholesterol and apolipoprotein ai Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma high density lipoprotein cholesterol and apolipoprotein ai in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high-density lipoprotein cholesterol Gene Set

From GAD Gene-Disease Associations

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

increased circulating high density lipoprotein cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased circulating high density lipoprotein cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low high-density lipoprotein cholesterol concentration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low high-density lipoprotein cholesterol concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased plasma triglyceride and lower high-density lipoprotein cholesterol concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased plasma triglyceride and lower high-density lipoprotein cholesterol concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease elevated serum apolipoprotein ai and high density lipoprotein cholesterol concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma high-density lipoprotein cholesterol levels Gene Set

From GAD Gene-Disease Associations

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

high-density lipoprotein-cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high-density lipoprotein-cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

plasma apolipoprotein ai (apoai) and high-density lipoprotein cholesterol (hdl) levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma apolipoprotein ai (apoai) and high-density lipoprotein cholesterol (hdl) levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

{high density lipoprotein cholesterol, low serum, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {high density lipoprotein cholesterol, low serum, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

cholesterol; cholesterol, hdl; triglycerides; cholesterol, ldl; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

{low density lipoprotein cholesterol level qtl 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {low density lipoprotein cholesterol level qtl 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

[low density lipoprotein cholesterol level qtl 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [low density lipoprotein cholesterol level qtl 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

[low density lipoprotein cholesterol level qtl6] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [low density lipoprotein cholesterol level qtl6] phenotype from the curated OMIM Gene-Disease Associations dataset.

quantitative variation in plasma high-density lipoproteins and triacylglycerides Gene Set

From GAD Gene-Disease Associations

genes associated with the disease quantitative variation in plasma high-density lipoproteins and triacylglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high-density lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the high-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

spherical high-density lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the spherical high-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

discoidal high-density lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the discoidal high-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

high-density lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the high-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

spherical high-density lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the spherical high-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

discoidal high-density lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the discoidal high-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

high density lipoprotein. Gene Set

From GAD Gene-Disease Associations

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

high density lipoprotein levels. Gene Set

From GAD Gene-Disease Associations

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

positive regulation of high-density lipoprotein particle assembly Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations dataset.

high-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

positive regulation of high-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

high-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the high-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

cellular response to high density lipoprotein particle stimulus Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to high density lipoprotein particle stimulus biological process from the curated GO Biological Process Annotations dataset.

high-density lipoprotein particle assembly Gene Set

From GO Biological Process Annotations

genes participating in the high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations dataset.

regulation of high-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

regulation of high-density lipoprotein particle assembly Gene Set

From GO Biological Process Annotations

genes participating in the regulation of high-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations dataset.

response to high density lipoprotein particle Gene Set

From GO Biological Process Annotations

genes participating in the response to high density lipoprotein particle biological process from the curated GO Biological Process Annotations dataset.

negative regulation of high-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of high-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

high-density lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

spherical high-density lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the spherical high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

discoidal high-density lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the discoidal high-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

high-density lipoprotein particle receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the high-density lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

high-density lipoprotein particle receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the high-density lipoprotein particle receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

high-density lipoprotein particle binding Gene Set

From GO Molecular Function Annotations

genes performing the high-density lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations dataset.

plasma apob and low density lipoprotein (ldl) cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease plasma apob and low density lipoprotein (ldl) cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total and low-density lipoprotein cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease total and low-density lipoprotein cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low-density lipoprotein cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low-density lipoprotein cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

receptor-mediated endocytosis of low-density lipoprotein particle involved in cholesterol transport Gene Set

From GO Biological Process Annotations

genes participating in the receptor-mediated endocytosis of low-density lipoprotein particle involved in cholesterol transport biological process from the curated GO Biological Process Annotations dataset.

increased circulating very-low-density lipoprotein cholesterol Gene Set

From HPO Gene-Disease Associations

genes associated with the increased circulating very-low-density lipoprotein cholesterol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

protein quantitative trait loci Gene Set

From GAD Gene-Disease Associations

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

Protein quantitative trait loci Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Protein quantitative trait loci phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Depression (quantitative trait) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Depression (quantitative trait) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

body mass; cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides Gene Set

From GAD Gene-Disease Associations

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

cholesterol; cholesterol, hdl; lipoprotein; lipids Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

cholesterol, hdl; triglycerides; cholesterol, ldl; lipoprotein; fatty acid; uric acid Gene Set

From GAD Gene-Disease Associations

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

cholesterol, ldl; cholesterol, total; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; cholesterol, ldl; cholesterol, total; apoa1; apoe; apob-100 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; cholesterol, ldl; cholesterol, total; apoa1; apoe; apob-100 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; cholesterol, hdl; cholesterol, ldl; hypertension; lipoproteins; obesity Gene Set

From GAD Gene-Disease Associations

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

cholesterol; cholesterol, hdl; atherosclerosis, coronary; cholesterol, ldl Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; cholesterol, hdl; atherosclerosis, coronary; cholesterol, ldl 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.

cholesterol, hdl; triglycerides; coronary heart disease; cholesterol, ldl; cholesterol, total Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; triglycerides; coronary heart disease; cholesterol, ldl; cholesterol, total 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.

cholesterol; cholesterol, hdl; cholesterol, ldl Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; cholesterol, hdl; cholesterol, ldl 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.

cholesterol; cholesterol, hdl; triglycerides; diabetes, type 2; ulcerative colitis; cholesterol, ldl; liver disease; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; cholesterol, hdl; triglycerides; diabetes, type 2; ulcerative colitis; cholesterol, ldl; liver disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol; cholesterol, hdl; cholesterol, ldl; triacylglycerol Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; cholesterol, ldl; cholesterol, vldl Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

abnormality of the level of lipoprotein cholesterol Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of the level of lipoprotein cholesterol phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of the level of lipoprotein cholesterol Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of the level of lipoprotein cholesterol phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

bone mineral density (bmd) / quantitative ultra sound (qus) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density (bmd) / quantitative ultra sound (qus) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

quantitative variation in lipid and lipoprotein traits Gene Set

From GAD Gene-Disease Associations

genes associated with the disease quantitative variation in lipid and lipoprotein traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; triglycerides; personality trait Gene Set

From GAD Gene-Disease Associations

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

high triglyceride/ low hdl cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high triglyceride/ low hdl cholesterol levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high and low levels of cholesterol Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high and low levels of cholesterol in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

low-density lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the low-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

intermediate-density lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the intermediate-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

very-low-density lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the very-low-density lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

low-density lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the low-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

intermediate-density lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the intermediate-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

very-low-density lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the very-low-density lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

very low density lipoprotein triglyceride Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical very low density lipoprotein triglyceride from the curated CTD Gene-Chemical Interactions dataset.

serum low-density lipoprotein metabolism Gene Set

From GAD Gene-Disease Associations

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

oxidized low-density lipoprotein and cardiolipin autoantibodies Gene Set

From GAD Gene-Disease Associations

genes associated with the disease oxidized low-density lipoprotein and cardiolipin autoantibodies in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

reduced low-density lipoprotein particle size Gene Set

From GAD Gene-Disease Associations

genes associated with the disease reduced low-density lipoprotein particle size in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

intermediate density lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

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

low-density lipoprotein receptor particle metabolic process Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein receptor particle metabolic process biological process from the curated GO Biological Process Annotations dataset.

negative regulation of low-density lipoprotein particle receptor catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of low-density lipoprotein particle receptor catabolic process biological process from the curated GO Biological Process Annotations dataset.

regulation of very-low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the regulation of very-low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

regulation of very-low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of very-low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

very-low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the very-low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

positive regulation of low-density lipoprotein particle receptor catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of low-density lipoprotein particle receptor catabolic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of very-low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of very-low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

response to low-density lipoprotein particle Gene Set

From GO Biological Process Annotations

genes participating in the response to low-density lipoprotein particle biological process from the curated GO Biological Process Annotations dataset.

positive regulation of low-density lipoprotein particle receptor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of low-density lipoprotein particle receptor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

intermediate-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the intermediate-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

negative regulation of low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

negative regulation of very-low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of very-low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle mediated signaling Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle mediated signaling biological process from the curated GO Biological Process Annotations dataset.

cellular response to low-density lipoprotein particle stimulus Gene Set

From GO Biological Process Annotations

genes participating in the cellular response to low-density lipoprotein particle stimulus biological process from the curated GO Biological Process Annotations dataset.

regulation of low-density lipoprotein particle receptor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of low-density lipoprotein particle receptor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

very-low-density lipoprotein particle assembly Gene Set

From GO Biological Process Annotations

genes participating in the very-low-density lipoprotein particle assembly biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle receptor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle receptor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

regulation of low-density lipoprotein particle receptor catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the regulation of low-density lipoprotein particle receptor catabolic process biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle receptor catabolic process Gene Set

From GO Biological Process Annotations

genes participating in the low-density lipoprotein particle receptor catabolic process biological process from the curated GO Biological Process Annotations dataset.

negative regulation of very-low-density lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of very-low-density lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

very-low-density lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the very-low-density lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

negative regulation of low-density lipoprotein particle receptor biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of low-density lipoprotein particle receptor biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

low-density lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the low-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

intermediate-density lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the intermediate-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

very-low-density lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the very-low-density lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

low-density lipoprotein particle binding Gene Set

From GO Molecular Function Annotations

genes performing the low-density lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations dataset.

very-low-density lipoprotein particle binding Gene Set

From GO Molecular Function Annotations

genes performing the very-low-density lipoprotein particle binding molecular function from the curated GO Molecular Function Annotations dataset.

very-low-density lipoprotein particle receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the very-low-density lipoprotein particle receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

low-density lipoprotein particle receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the low-density lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

very-low-density lipoprotein particle receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the very-low-density lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

low-density lipoprotein receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the low-density lipoprotein receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

Low-density lipoprotein (LDL) receptor class A, conserved site Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Low-density lipoprotein (LDL) receptor class A, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Low density lipoprotein receptor-related protein, 5/6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Low density lipoprotein receptor-related protein, 5/6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Low-density lipoprotein (LDL) receptor class A repeat Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Low-density lipoprotein (LDL) receptor class A repeat protein domain from the InterPro Predicted Protein Domain Annotations 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.

cholesterol, hdl; lipoprotein, ldl Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; triglycerides; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

cholesterol; triglycerides; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

cholesterol; lipoprotein, ldl; atherosclerosis, coronary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; lipoprotein, ldl; atherosclerosis, coronary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, ldl; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

lipoprotein, ldl; cholesterol, ldl Gene Set

From GAD Gene-Disease Associations

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

cholesterol, ldl; cholesterol, total; apolipoproteins Gene Set

From GAD Gene-Disease Associations

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

cholesterol; triglycerides; diabetes, type 2; cholesterol, ldl; lipoproteins; indulinh Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; triglycerides; diabetes, type 2; cholesterol, ldl; lipoproteins; indulinh in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; cholesterol, ldl; cholesterol, total; insulin; apob Gene Set

From GAD Gene-Disease Associations

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

cholesterol; cholesterol, hdl; triglycerides Gene Set

From GAD Gene-Disease Associations

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

cholesterol; triglycerides; cholesterol, ldl Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; triglycerides; cholesterol, ldl in GWAS and other genetic association datasets from the GAD 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.

cholesterol; cholesterol, ldl; campesterol; sitosterol Gene Set

From GAD Gene-Disease Associations

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

diabetes, type 2; cholesterol, ldl; cholesterol, total; insulin Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl Gene Set

From GAD Gene-Disease Associations

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

cholesterol, ldl; cholesterol, total Gene Set

From GAD Gene-Disease Associations

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

cholesterol; hypercholesterolemia; cholesterol, ldl; hypertriglyceridemia Gene Set

From GAD Gene-Disease Associations

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

cholesterol; cholesterol, ldl; lipoproteins; fatty acid Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol; cholesterol, ldl; lipoproteins; fatty acid in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; cholesterol, total; insulin; cortisol Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; cholesterol, ldl; lathosterol Gene Set

From GAD Gene-Disease Associations

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

cholesterol; cholesterol, ldl; carotid atherosclerosis Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; cholesterol, ldl; apoa1; apob Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; cholesterol, ldl; apoa1; apob in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

total cholesterol and ldl-cholesterol Gene Set

From GAD Gene-Disease Associations

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

body mass; cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl; hypertension; atherosclerosis Gene Set

From GAD Gene-Disease Associations

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

cholesterol, ldl; cholesterol, total; insulin sensitivity; hyperinsulinemia Gene Set

From GAD Gene-Disease Associations

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

cholesterol, ldl; cholesterol, total; apob; apoai Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; triglycerides; cholesterol, ldl Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; cholesterol, ldl Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; cholesterol, ldl; breast cancer Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; cholesterol, ldl; leukemia; 9-hydroxyrisperidone; risperidone Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, hdl; cholesterol, ldl; leukemia; 9-hydroxyrisperidone; risperidone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; cholesterol, ldl; lipids Gene Set

From GAD Gene-Disease Associations

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

cholesterol; cholesterol, ldl Gene Set

From GAD Gene-Disease Associations

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

cholesterol, hdl; cholesterol, vldl Gene Set

From GAD Gene-Disease Associations

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

cholesterol, ldl; cholesterol, total; c-reactive protein; apoa2; apob Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cholesterol, ldl; cholesterol, total; c-reactive protein; apoa2; apob in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cholesterol, hdl; arterial-wall changes; cholesterol efflux Gene Set

From GAD Gene-Disease Associations

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

serum cholesterol and ldl-cholesterol levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum cholesterol and ldl-cholesterol levels 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.

cholesterol, hdl; triglycerides; cholesterol, total Gene Set

From GAD Gene-Disease Associations

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

cholesterol; cholesterol, ldl; insulin; apob Gene Set

From GAD Gene-Disease Associations

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

lipoprotein level Gene Set

From GAD Gene-Disease Associations

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

abnormal circulating lipoprotein level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal lipoprotein level Gene Set

From MPO Gene-Phenotype Associations

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

hdl-cholesterol level Gene Set

From GAD Gene-Disease Associations

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

abnormal liver cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

increased cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

increased circulating vldl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

decreased circulating hdl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

decreased liver cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

increased brain cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

increased circulating hdl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

increased circulating ldl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating vldl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating ldl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

decreased cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating hdl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating non-hdl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

decreased circulating cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

decreased circulating vldl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

increased liver cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal brain cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

decreased brain cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

decreased circulating ldl cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

increased circulating cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

abnormal circulating cholesterol level Gene Set

From MPO Gene-Phenotype Associations

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

ldl cholesterol level qtl2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ldl cholesterol level qtl2 phenotype from the curated OMIM Gene-Disease Associations dataset.

[cholesterol level qtl 1] Gene Set

From OMIM Gene-Disease Associations

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

[cholesterol level qtl 2] Gene Set

From OMIM Gene-Disease Associations

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

quantitative calcaneal ultrasound Gene Set

From GAD Gene-Disease Associations

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

quantitative traits Gene Set

From GAD Gene-Disease Associations

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

quantitative calcaneal ultrasounds Gene Set

From GAD Gene-Disease Associations

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

biomedical quantitative traits Gene Set

From GAD Gene-Disease Associations

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

quantitative Gene Set

From GeneRIF Biological Term Annotations

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

Biomedical quantitative traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Biomedical quantitative traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Quantitative traits Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

locus ceruleus, right Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in locus ceruleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

locus ceruleus, left Gene Set

From Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles

genes with high or low expression in locus ceruleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.

locus coeruleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in locus coeruleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

Locus ceruleus Gene Set

From Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles

genes with high or low expression in Locus ceruleus relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.

histone locus body Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the histone locus body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

histone locus body Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

bcli restriction fragment length polymorphism at the glucocorticoid receptor gene locus Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bcli restriction fragment length polymorphism at the glucocorticoid receptor gene locus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cd3 epsilon locus on chromosome 11 Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cd3 epsilon locus on chromosome 11 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

locus Gene Set

From GeneRIF Biological Term Annotations

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

somatic diversification of immune receptors via germline recombination within a single locus Gene Set

From GO Biological Process Annotations

genes participating in the somatic diversification of immune receptors via germline recombination within a single locus biological process from the curated GO Biological Process Annotations dataset.

locus ceruleus development Gene Set

From GO Biological Process Annotations

genes participating in the locus ceruleus development biological process from the curated GO Biological Process Annotations dataset.

histone locus body Gene Set

From GO Cellular Component Annotations

proteins localized to the histone locus body cellular component from the curated GO Cellular Component Annotations dataset.

MDS1-EVI1 complex locus protein MDS1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the MDS1-EVI1 complex locus protein MDS1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

SCL-interrupting locus protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the SCL-interrupting locus protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lymphocyte antigen 6 complex locus protein G6d/G6f Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lymphocyte antigen 6 complex locus protein G6d/G6f protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Surfeit locus 6 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Surfeit locus 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Surfeit locus 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Surfeit locus 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neurogenic locus Notch 1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neurogenic locus Notch 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neurogenic locus Notch 3 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neurogenic locus Notch 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neurogenic locus Notch 2 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neurogenic locus Notch 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Surfeit locus 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Surfeit locus 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Ribosomal RNA-processing protein 14/surfeit locus protein 6, C-terminal domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Lymphocyte antigen 6 complex locus protein G5c Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lymphocyte antigen 6 complex locus protein G5c protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Surfeit locus 1/Shy1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Surfeit locus 1/Shy1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Neurogenic locus Notch 4 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Neurogenic locus Notch 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

abnormal locus ceruleus morphology Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal locus ceruleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

locus ceruleus Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue locus ceruleus in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

Alpha trait thalassemia Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha trait thalassemia phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

NOVELTY SEEKING PERSONALITY TRAIT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease NOVELTY SEEKING PERSONALITY TRAIT from the curated CTD Gene-Disease Associations dataset.

PREMATURE CHROMATID SEPARATION TRAIT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PREMATURE CHROMATID SEPARATION TRAIT from the curated CTD Gene-Disease Associations dataset.

anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; beta-thalassemia; sickle cell trait; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; anemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

malaria, falciparum; parasitemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease malaria, falciparum; parasitemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

beta thalassemia; beta-thalassemia; heterozygous haemoglobin s; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; heterozygous haemoglobin s; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heterozygous haemoglobin s; malaria; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heterozygous haemoglobin s; malaria; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nicotine; personality trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease nicotine; personality trait 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.

anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia; anemia, sickle cell; hemoglobin c disease; hemoglobin sc disease; heterozygous haemoglobin s; malaria, falciparum; parasitemia; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

personality trait Gene Set

From GAD Gene-Disease Associations

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

personality trait, 'novelty seeking' Gene Set

From GAD Gene-Disease Associations

genes associated with the disease personality trait, 'novelty seeking' in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

personality trait detachment Gene Set

From GAD Gene-Disease Associations

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

anemia, sickle cell; heterozygous haemoglobin s; malaria; sickle cell anemia; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anemia, sickle cell; heterozygous haemoglobin s; malaria; sickle cell anemia; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alpha-thalassemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alpha-thalassemia; glucosephosphate dehydrogenase deficiency; malaria, falciparum; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

personality trait and intelligence Gene Set

From GAD Gene-Disease Associations

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

personality trait of spritual acceptance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease personality trait of spritual acceptance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cognitive trait Gene Set

From GAD Gene-Disease Associations

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

impulsive trait Gene Set

From GAD Gene-Disease Associations

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

adaptability trait Gene Set

From GAD Gene-Disease Associations

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

beta thalassemia; beta-thalassemia; hemoglobin sc disease; heterozygous haemoglobin s; sickle cell trait Gene Set

From GAD Gene-Disease Associations

genes associated with the disease beta thalassemia; beta-thalassemia; hemoglobin sc disease; heterozygous haemoglobin s; sickle cell trait in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

trait Gene Set

From GeneRIF Biological Term Annotations

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

obsessive-compulsive trait Gene Set

From HPO Gene-Disease Associations

genes associated with the obsessive-compulsive trait phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Sickle Cell Trait Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Sickle Cell Trait phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

[premature chromatid separation trait] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [premature chromatid separation trait] phenotype from the curated OMIM Gene-Disease Associations dataset.

Deafness, high-frequency sensorineural, X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, high-frequency sensorineural, X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

High bone mass Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the High bone mass phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopia, high, with cataract and vitreoretinal degeneration Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

high-affinity iron permease complex Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the high-affinity iron permease complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

DJ-1-SNCA complex, high molecular weight complex Gene Set

From CORUM Protein Complexes

proteins in the DJ-1-SNCA complex, high molecular weight complex protein complex from the CORUM Protein Complexes dataset.

ultra-high molecular weight polyethylene Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical ultra-high molecular weight polyethylene from the curated CTD Gene-Chemical Interactions dataset.

Cardiac Output, High Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cardiac Output, High from the curated CTD Gene-Disease Associations dataset.

high pressure neurological syndrome Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease high pressure neurological syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

high serum ige concentrations Gene Set

From GAD Gene-Disease Associations

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

glioma (high-grade) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease glioma (high-grade) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high insulin concentrations in non-diabetic mexican ameri Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high insulin concentrations in non-diabetic mexican ameri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high ethanol tolerance Gene Set

From GAD Gene-Disease Associations

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

high plasma cetp activity. Gene Set

From GAD Gene-Disease Associations

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

hearing impairment; hearing loss; hearing loss, high-frequency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; hearing loss, high-frequency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma; candidiasis; high-altitude illness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma; candidiasis; high-altitude illness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high tnf levels is not a risk factor for venous thromboem Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high tnf levels is not a risk factor for venous thromboem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neuroblastoma (high-risk) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neuroblastoma (high-risk) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing disorders; hearing loss, high-frequency; hearing problem Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing disorders; hearing loss, high-frequency; hearing problem in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high plasma factor viii: c levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high plasma factor viii: c levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high interleukin-1 beta plasma levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high interleukin-1 beta plasma levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high neuroticism and low agreeableness Gene Set

From GAD Gene-Disease Associations

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

high altitude performance Gene Set

From GAD Gene-Disease Associations

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

lymph node involvement and other histopathological indicators of high metastatic potential Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymph node involvement and other histopathological indicators of high metastatic potential in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high frequency of factor v leiden mutation. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high frequency of factor v leiden mutation. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high coronary heart disease risk particularly affects ser Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high coronary heart disease risk particularly affects ser in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high-grade soft tissue sarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high-grade soft tissue sarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high exposure to aflatoxin b1. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high exposure to aflatoxin b1. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high-altitude illness Gene Set

From GAD Gene-Disease Associations

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

high-monounsaturated fatty acid diet Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high-monounsaturated fatty acid diet in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high or low factor xiii specific activity. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high or low factor xiii specific activity. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

high-altitude pulmonary edema. Gene Set

From GAD Gene-Disease Associations

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

high total ige Gene Set

From GAD Gene-Disease Associations

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

high inducibility of cytochrome p450 1a1 gene transcription Gene Set

From GAD Gene-Disease Associations

genes associated with the disease high inducibility of cytochrome p450 1a1 gene transcription in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

AIRE_KO_GDS2274_246_mouse_Medullary thymic epithelial cells (with high CD80 expression) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the AIRE_KO_GDS2274_246_mouse_Medullary thymic epithelial cells (with high CD80 expression) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

regulation of high voltage-gated calcium channel activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of high voltage-gated calcium channel activity biological process from the curated GO Biological Process Annotations dataset.

response to high light intensity Gene Set

From GO Biological Process Annotations

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

lymphocyte chemotaxis across high endothelial venule Gene Set

From GO Biological Process Annotations

genes participating in the lymphocyte chemotaxis across high endothelial venule biological process from the curated GO Biological Process Annotations dataset.

b cell chemotaxis across high endothelial venule Gene Set

From GO Biological Process Annotations

genes participating in the b cell chemotaxis across high endothelial venule biological process from the curated GO Biological Process Annotations dataset.

high-affinity l-ornithine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity l-ornithine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity lysine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity lysine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity sodium:dicarboxylate symporter activity Gene Set

From GO Molecular Function Annotations

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

high voltage-gated calcium channel activity Gene Set

From GO Molecular Function Annotations

genes performing the high voltage-gated calcium channel activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity basic amino acid transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity basic amino acid transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high molecular weight b cell growth factor receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the high molecular weight b cell growth factor receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity inorganic phosphate:sodium symporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity inorganic phosphate:sodium symporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity arginine transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity arginine transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity glutamate transmembrane transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity glutamate transmembrane transporter activity molecular function from the curated GO Molecular Function Annotations dataset.

high-affinity oligopeptide transporter activity Gene Set

From GO Molecular Function Annotations

genes performing the high-affinity oligopeptide transporter activity molecular function from the curated GO Molecular Function Annotations 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.

Neuroblastoma (high-risk) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Neuroblastoma (high-risk) 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.

Glioma (high-grade) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Glioma (high-grade) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

high-frequency hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the high-frequency hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high iliac wings Gene Set

From HPO Gene-Disease Associations

genes associated with the high iliac wings phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high palate Gene Set

From HPO Gene-Disease Associations

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

high axial triradius Gene Set

From HPO Gene-Disease Associations

genes associated with the high axial triradius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high nonceruloplasmin-bound serum copper Gene Set

From HPO Gene-Disease Associations

genes associated with the high nonceruloplasmin-bound serum copper phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high maternal serum alpha-fetoprotein Gene Set

From HPO Gene-Disease Associations

genes associated with the high maternal serum alpha-fetoprotein phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high, narrow palate Gene Set

From HPO Gene-Disease Associations

genes associated with the high, narrow palate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high-frequency sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the high-frequency sensorineural hearing impairment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high-output congestive heart failure Gene Set

From HPO Gene-Disease Associations

genes associated with the high-output congestive heart failure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high anterior hairline Gene Set

From HPO Gene-Disease Associations

genes associated with the high anterior hairline phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high pitched voice Gene Set

From HPO Gene-Disease Associations

genes associated with the high pitched voice phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

high forehead Gene Set

From HPO Gene-Disease Associations

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

high-grade hypermetropia Gene Set

From HPO Gene-Disease Associations

genes associated with the high-grade hypermetropia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Hearing Loss, High-Frequency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Hearing Loss, High-Frequency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

High affinity immunoglobulin epsilon receptor subunit beta Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High affinity immunoglobulin epsilon receptor subunit beta protein domain from the InterPro Predicted Protein Domain Annotations dataset.

T-cell surface glycoprotein CD3 zeta/eta subunit/High affinity IgE receptor gamma subunit Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the T-cell surface glycoprotein CD3 zeta/eta subunit/High affinity IgE receptor gamma subunit protein domain from the InterPro Predicted Protein Domain Annotations dataset.

Keratin, high-sulphur matrix protein Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Keratin, high-sulphur matrix protein protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group box domain Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group box domain protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group, HMG-I/HMG-Y Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group, HMG-I/HMG-Y protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group nucleosome-binding domain-containing family Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group nucleosome-binding domain-containing family protein domain from the InterPro Predicted Protein Domain Annotations dataset.

High mobility group box domain 5 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the High mobility group box domain 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

high palate Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the high palate phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

high mean erythrocyte cell number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the high mean erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal ly6c high monocyte number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal ly6c high monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased ly6c high monocyte number Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased ly6c high monocyte number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

myopia, high, with cataract and vitreoretinal degeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopia, high, with cataract and vitreoretinal degeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

[hemoglobin, high altitude adaptation] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [hemoglobin, high altitude adaptation] phenotype from the curated OMIM Gene-Disease Associations dataset.

[high molecular weight kininogen deficiency] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [high molecular weight kininogen deficiency] phenotype from the curated OMIM Gene-Disease Associations dataset.

[gamma-glutamyltransferase, familial high serum] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [gamma-glutamyltransferase, familial high serum] phenotype from the curated OMIM Gene-Disease Associations dataset.

b-cell non-hodgkin lymphoma, high-grade Gene Set

From OMIM Gene-Disease Associations

genes associated with the b-cell non-hodgkin lymphoma, high-grade phenotype from the curated OMIM Gene-Disease Associations dataset.

high endothelial venule Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue high endothelial venule in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

high vocal center Gene Set

From TISSUES Text-mining Tissue Protein Expression Evidence Scores

proteins co-occuring with the tissue high vocal center in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset.

postsynaptic density Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the postsynaptic density cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

postsynaptic density Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

Bone Density Gene Set

From dbGAP Gene-Trait Associations

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

calcium homeostasis and peripheral bone density Gene Set

From GAD Gene-Disease Associations

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

bone density Gene Set

From GAD Gene-Disease Associations

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

spinal bone mineral density Gene Set

From GAD Gene-Disease Associations

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

bone density; fractures, vertebral Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fractures, vertebral in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mammographic density Gene Set

From GAD Gene-Disease Associations

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

bone density; muscle strength Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; muscle strength in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; osteopenia Gene Set

From GAD Gene-Disease Associations

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

osteoporosis, postmenopausal; bone density; hormone disturbance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis, postmenopausal; bone density; hormone disturbance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mamographic density Gene Set

From GAD Gene-Disease Associations

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

colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease colorectal cancer; tourette syndrome; bone density; pregnancy loss, recurrent; cleft lip without cleft palate; juvenile polyposis; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; bone responsiveness Gene Set

From GAD Gene-Disease Associations

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

bone density but not spondylosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density but not spondylosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; bone mineral density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity; bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

platelet receptor density and the response to sfllrn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease platelet receptor density and the response to sfllrn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; fracture risk Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fracture risk in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

breast density Gene Set

From GAD Gene-Disease Associations

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

bone mineral density (spine) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density (spine) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

platelet alpha2 beta1 density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease platelet alpha2 beta1 density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dopamine d2 receptor density; monoamine metabolite concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dopamine d2 receptor density; monoamine metabolite concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

verbal learning, verbal memory, and regional cortical gray matter density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease verbal learning, verbal memory, and regional cortical gray matter density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; spondylosis, lumbar Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; spondylosis, lumbar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body mass; bone density Gene Set

From GAD Gene-Disease Associations

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

bone mineral density (bmd) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density (bmd) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; osteoporosis Gene Set

From GAD Gene-Disease Associations

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

bone density and spondylosis Gene Set

From GAD Gene-Disease Associations

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

bone density; fractures; osteocalcin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; fractures; osteocalcin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; calcium; fractures, nonvertebral; milk intolerance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; calcium; fractures, nonvertebral; milk intolerance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density dehydroepiandrosterone sulphate osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density dehydroepiandrosterone sulphate osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; fractures Gene Set

From GAD Gene-Disease Associations

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

variation in platelet integrin alpha 2 beta 1 density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease variation in platelet integrin alpha 2 beta 1 density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; height Gene Set

From GAD Gene-Disease Associations

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

low bone-mineral density and rapid postmenopausal bone loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease low bone-mineral density and rapid postmenopausal bone loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

coronary heart disease and serum very low density lipopro Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary heart disease and serum very low density lipopro in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammatory bowel disease; bone density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease inflammatory bowel disease; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; coronary calcification Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; coronary calcification in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone density; tricho-dento-osseous syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; tricho-dento-osseous syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineral density (hip) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density (hip) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

testosterone; bone density; stature Gene Set

From GAD Gene-Disease Associations

genes associated with the disease testosterone; bone density; stature in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone mineral density ; osteoporosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone mineral density ; osteoporosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

osteoporosis, postmenopausal; bone density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease osteoporosis, postmenopausal; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mammographic breast density Gene Set

From GAD Gene-Disease Associations

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

bone mineral density Gene Set

From GAD Gene-Disease Associations

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

bone density; height; pth; pyridinoline, urinary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone density; height; pth; pyridinoline, urinary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

leukemia ; bone mineral density Gene Set

From GAD Gene-Disease Associations

genes associated with the disease leukemia ; bone mineral density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

density Gene Set

From GeneRIF Biological Term Annotations

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

postsynaptic density protein 95 clustering Gene Set

From GO Biological Process Annotations

genes participating in the postsynaptic density protein 95 clustering biological process from the curated GO Biological Process Annotations dataset.

postsynaptic density organization Gene Set

From GO Biological Process Annotations

genes participating in the postsynaptic density organization biological process from the curated GO Biological Process Annotations dataset.

detection of cell density Gene Set

From GO Biological Process Annotations

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

detection of cell density by contact stimulus involved in contact inhibition Gene Set

From GO Biological Process Annotations

genes participating in the detection of cell density by contact stimulus involved in contact inhibition biological process from the curated GO Biological Process Annotations dataset.

postsynaptic density assembly Gene Set

From GO Biological Process Annotations

genes participating in the postsynaptic density assembly biological process from the curated GO Biological Process Annotations dataset.

regulation of postsynaptic density protein 95 clustering Gene Set

From GO Biological Process Annotations

genes participating in the regulation of postsynaptic density protein 95 clustering biological process from the curated GO Biological Process Annotations dataset.

detection of cell density by contact stimulus Gene Set

From GO Biological Process Annotations

genes participating in the detection of cell density by contact stimulus biological process from the curated GO Biological Process Annotations dataset.

neuronal postsynaptic density Gene Set

From GO Cellular Component Annotations

proteins localized to the neuronal postsynaptic density cellular component from the curated GO Cellular Component Annotations dataset.

postsynaptic density Gene Set

From GO Cellular Component Annotations

proteins localized to the postsynaptic density cellular component from the curated GO Cellular Component Annotations dataset.

Mammographic density Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

Bone mineral density (paediatric, upper limb) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, upper limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (hip) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (hip) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (paediatric, total body less head) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, total body less head) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (paediatric, skull) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, skull) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (paediatric, lower limb) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (paediatric, lower limb) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density (spine) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density (spine) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Bone mineral density Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Bone mineral density phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

increased density of long bones Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the increased density of long bones phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

reduced bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the reduced bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

patchy changes of bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the patchy changes of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

abnormality of bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the abnormality of bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

increased bone mineral density Gene Set

From GWASdb SNP-Phenotype Associations

genes associated with the increased bone mineral density phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

increased bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the increased bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patchy changes of bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy changes of bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased density of long bones Gene Set

From HPO Gene-Disease Associations

genes associated with the increased density of long bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the abnormality of bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

increased density of long bone diaphyses Gene Set

From HPO Gene-Disease Associations

genes associated with the increased density of long bone diaphyses phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

reduced bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the reduced bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

patchy variation in bone mineral density Gene Set

From HPO Gene-Disease Associations

genes associated with the patchy variation in bone mineral density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

abnormality of hair density Gene Set

From HPO Gene-Disease Associations

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

Density-regulated protein DRP1 Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Density-regulated protein DRP1 protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased bone mineral density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased bone mineral density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone mineral density of femur Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone mineral density of femur phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased trabecular bone connectivity density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased trabecular bone connectivity density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased skeletal muscle fiber density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased skeletal muscle fiber density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased bone mineral density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased bone mineral density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal bone mineral density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal bone mineral density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased trabecular bone connectivity density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased trabecular bone connectivity density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal trabecular bone connectivity density Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal trabecular bone connectivity density phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

bone mineral density qtl18, osteoporosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the bone mineral density qtl18, osteoporosis phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density variability 1] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density variability 1] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 11] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 11] phenotype from the curated OMIM Gene-Disease Associations dataset.

{bone mineral density qtl 12, osteoporosis} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bone mineral density qtl 12, osteoporosis} phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 13] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 13] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 15] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 15] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 3] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 3] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 5] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 5] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 9] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 9] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 6] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 6] phenotype from the curated OMIM Gene-Disease Associations dataset.

dopamine receptor d2, reduced brain density of Gene Set

From OMIM Gene-Disease Associations

genes associated with the dopamine receptor d2, reduced brain density of phenotype from the curated OMIM Gene-Disease Associations dataset.

{bone mineral density, low, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bone mineral density, low, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 10] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 10] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 2] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 2] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 14] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 14] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density variation qtl] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density variation qtl] phenotype from the curated OMIM Gene-Disease Associations dataset.

[bone mineral density qtl 4] Gene Set

From OMIM Gene-Disease Associations

genes associated with the [bone mineral density qtl 4] phenotype from the curated OMIM Gene-Disease Associations dataset.

LIPOPROTEIN(a) DEFICIENCY, CONGENITAL Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the LIPOPROTEIN(a) DEFICIENCY, CONGENITAL phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

triglyceride-rich lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the triglyceride-rich lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

plasma lipoprotein particle Gene Set

From COMPARTMENTS Curated Protein Localization Evidence Scores

proteins localized to the plasma lipoprotein particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.

plasma lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

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

triglyceride-rich lipoprotein particle Gene Set

From COMPARTMENTS Text-mining Protein Localization Evidence Scores

proteins co-occuring with the triglyceride-rich lipoprotein particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.

FSL-1 lipoprotein, synthetic Gene Set

From CTD Gene-Chemical Interactions

genes/proteins interacting with the chemical FSL-1 lipoprotein, synthetic from the curated CTD Gene-Chemical Interactions dataset.

Lipoprotein Glomerulopathy Gene Set

From CTD Gene-Disease Associations

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

lipoprotein A-I [Supplementary Concept] Gene Set

From dbGAP Gene-Trait Associations

genes associated with the trait lipoprotein A-I [Supplementary Concept] in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset.

Lipoprotein(a) Gene Set

From dbGAP Gene-Trait Associations

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

familial lipoprotein lipase deficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease familial lipoprotein lipase deficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

familial lipoprotein lipase deficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease familial lipoprotein lipase deficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

OspA lipoprotein Gene Set

From DrugBank Drug Targets

interacting proteins for the OspA lipoprotein drug from the curated DrugBank Drug Targets dataset.

postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene Set

From GAD Gene-Disease Associations

genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipoprotein distribution of apoc-i Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipoprotein distribution of apoc-i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipoprotein(a) Gene Set

From GAD Gene-Disease Associations

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

heart disease, ischemic; lipoprotein Gene Set

From GAD Gene-Disease Associations

genes associated with the disease heart disease, ischemic; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, coronary; lipoprotein; lipids Gene Set

From GAD Gene-Disease Associations

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

coronary artery reactivity; lipoprotein oxidation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease coronary artery reactivity; lipoprotein oxidation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, coronary; diabetes, type 2; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

serum lipoprotein lipid and apolipoprotein levels Gene Set

From GAD Gene-Disease Associations

genes associated with the disease serum lipoprotein lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

differential plasma lipoprotein response to simvastatin Gene Set

From GAD Gene-Disease Associations

genes associated with the disease differential plasma lipoprotein response to simvastatin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipoprotein (a) concentration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipoprotein (a) concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

myocardial infarct; lipoprotein; cerebral infarct Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; lipoprotein; cerebral infarct in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipoprotein(a) concentration Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipoprotein(a) concentration in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypolipoproteinemias; lipoprotein; deficiency Gene Set

From GAD Gene-Disease Associations

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

lipoprotein Gene Set

From GAD Gene-Disease Associations

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

diabetes, type 2; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

lower lipoprotein lipase activity Gene Set

From GAD Gene-Disease Associations

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

lipoprotein a-i Gene Set

From GAD Gene-Disease Associations

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

lipoprotein; antiphospholipid syndrome Gene Set

From GAD Gene-Disease Associations

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

plasma lipoprotein(a) levels Gene Set

From GAD Gene-Disease Associations

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

myocardial infarct; lipoprotein; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease myocardial infarct; lipoprotein; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

lipoprotein, ldl Gene Set

From GAD Gene-Disease Associations

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

insulin; lipoprotein; lipids Gene Set

From GAD Gene-Disease Associations

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

lipoprotein; lipids Gene Set

From GAD Gene-Disease Associations

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

lipoprotein subclass profiles Gene Set

From GAD Gene-Disease Associations

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

anti-atherogenic lipoprotein profile Gene Set

From GAD Gene-Disease Associations

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

triglycerides; diabetes, type 2; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

lipoprotein, ldl; lipids; preeclampsia; apolipoproteins Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lipoprotein, ldl; lipids; preeclampsia; apolipoproteins in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

triglycerides; atherosclerosis, coronary; lipoprotein Gene Set

From GAD Gene-Disease Associations

genes associated with the disease triglycerides; atherosclerosis, coronary; lipoprotein in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

atherosclerosis, coronary; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

lipoprotein levels Gene Set

From GAD Gene-Disease Associations

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

lipoprotein glomerulopathy Gene Set

From GAD Gene-Disease Associations

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

plasma lipoprotein traits Gene Set

From GAD Gene-Disease Associations

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

triglycerides; lipoprotein Gene Set

From GAD Gene-Disease Associations

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

lipoprotein Gene Set

From GeneRIF Biological Term Annotations

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

negative regulation of lipoprotein oxidation Gene Set

From GO Biological Process Annotations

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

positive regulation of lipoprotein lipase activity Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations dataset.

regulation of lipoprotein metabolic process Gene Set

From GO Biological Process Annotations

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

lipoprotein particle mediated signaling Gene Set

From GO Biological Process Annotations

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

lipoprotein metabolic process Gene Set

From GO Biological Process Annotations

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

plasma lipoprotein particle assembly Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle assembly biological process from the curated GO Biological Process Annotations dataset.

negative regulation of lipoprotein lipase activity Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations dataset.

regulation of lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

lipoprotein modification Gene Set

From GO Biological Process Annotations

genes participating in the lipoprotein modification biological process from the curated GO Biological Process Annotations dataset.

negative regulation of plasma lipoprotein particle oxidation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations dataset.

regulation of lipoprotein oxidation Gene Set

From GO Biological Process Annotations

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

response to bacterial lipoprotein Gene Set

From GO Biological Process Annotations

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

regulation of lipoprotein lipase activity Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lipoprotein lipase activity biological process from the curated GO Biological Process Annotations dataset.

regulation of lipoprotein lipid oxidation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations dataset.

lipoprotein localization Gene Set

From GO Biological Process Annotations

genes participating in the lipoprotein localization biological process from the curated GO Biological Process Annotations dataset.

lipoprotein biosynthetic process Gene Set

From GO Biological Process Annotations

genes participating in the lipoprotein biosynthetic process biological process from the curated GO Biological Process Annotations dataset.

positive regulation of lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

regulation of plasma lipoprotein particle levels Gene Set

From GO Biological Process Annotations

genes participating in the regulation of plasma lipoprotein particle levels biological process from the curated GO Biological Process Annotations dataset.

plasma lipoprotein particle organization Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle organization biological process from the curated GO Biological Process Annotations dataset.

positive regulation of lipoprotein metabolic process Gene Set

From GO Biological Process Annotations

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

triglyceride-rich lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the triglyceride-rich lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

regulation of plasma lipoprotein particle oxidation Gene Set

From GO Biological Process Annotations

genes participating in the regulation of plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

lipoprotein transport Gene Set

From GO Biological Process Annotations

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

plasma lipoprotein particle clearance Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle clearance biological process from the curated GO Biological Process Annotations dataset.

cellular response to bacterial lipoprotein Gene Set

From GO Biological Process Annotations

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

lipoprotein catabolic process Gene Set

From GO Biological Process Annotations

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

triglyceride-rich lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the triglyceride-rich lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

negative regulation of lipoprotein lipid oxidation Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations dataset.

lipoprotein oxidation Gene Set

From GO Biological Process Annotations

genes participating in the lipoprotein oxidation biological process from the curated GO Biological Process Annotations dataset.

detection of bacterial lipoprotein Gene Set

From GO Biological Process Annotations

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

plasma lipoprotein particle remodeling Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle remodeling biological process from the curated GO Biological Process Annotations dataset.

response to lipoprotein particle Gene Set

From GO Biological Process Annotations

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

negative regulation of lipoprotein metabolic process Gene Set

From GO Biological Process Annotations

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

plasma lipoprotein particle oxidation Gene Set

From GO Biological Process Annotations

genes participating in the plasma lipoprotein particle oxidation biological process from the curated GO Biological Process Annotations dataset.

cellular response to lipoprotein particle stimulus Gene Set

From GO Biological Process Annotations

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

plasma lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the plasma lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

triglyceride-rich lipoprotein particle Gene Set

From GO Cellular Component Annotations

proteins localized to the triglyceride-rich lipoprotein particle cellular component from the curated GO Cellular Component Annotations dataset.

lipoprotein particle receptor activity Gene Set

From GO Molecular Function Annotations

genes performing the lipoprotein particle receptor activity molecular function from the curated GO Molecular Function Annotations dataset.

lipoprotein transporter activity Gene Set

From GO Molecular Function Annotations

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

lipoprotein lipase activator activity Gene Set

From GO Molecular Function Annotations

genes performing the lipoprotein lipase activator activity molecular function from the curated GO Molecular Function Annotations dataset.

lipoprotein particle binding Gene Set

From GO Molecular Function Annotations

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

lipoprotein particle receptor binding Gene Set

From GO Molecular Function Annotations

genes performing the lipoprotein particle receptor binding molecular function from the curated GO Molecular Function Annotations dataset.

lipoprotein lipase activity Gene Set

From GO Molecular Function Annotations

genes performing the lipoprotein lipase activity molecular function from the curated GO Molecular Function Annotations dataset.

Lipoprotein-associated phospholipase A2 activity change in response to statin therapy Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Lipoprotein-associated phospholipase A2 activity change in response to statin therapy phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Lipoprotein-associated phospholipase A2 activity and mass Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Lipoprotein-associated phospholipase A2 activity and mass phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Lipoprotein lipase Gene Set

From InterPro Predicted Protein Domain Annotations

proteins predicted to have the Lipoprotein lipase protein domain from the InterPro Predicted Protein Domain Annotations dataset.

increased lipoprotein lipase activity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased lipoprotein lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased lipoprotein lipase activity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased lipoprotein lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal lipoprotein lipase activity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal lipoprotein lipase activity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

lipoprotein lipase deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipoprotein lipase deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

lipoprotein glomerulopathy Gene Set

From OMIM Gene-Disease Associations

genes associated with the lipoprotein glomerulopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

Lipoprotein metabolism Gene Set

From Reactome Pathways

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

Cholesterol monooxygenase (side-chain cleaving) deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cholesterol monooxygenase (side-chain cleaving) deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cholesterol, HDL Gene Set

From CTD Gene-Chemical Interactions

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

Cholesterol Gene Set

From CTD Gene-Chemical Interactions

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