Name

CIHL Gene

hearing loss, cisplatin-induced, susceptibility to

MCDR4 Gene

macular dystrophy, retinal, 4 (North Carolina type with progressive sensorineural hearing loss)

ARHI1 Gene

Age-related hearing impairment 1

ARHI2 Gene

Age-related hearing impairment 2

RDPA Gene

refsum disease, adult, with increased pipecolicacidemia

LOC105375354 Gene

postmeiotic segregation increased 2-like protein 5

IST1 Gene

increased sodium tolerance 1 homolog (yeast)

This gene encodes a protein with MIT-interacting motifs that interacts with components of endosomal sorting complexes required for transport (ESCRT). ESCRT functions in vesicle budding, such as that which occurs during membrane abscission in cytokinesis. There is a pseudogene for this gene on chromosome 19. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Aug 2012]

PMS2P8 Gene

postmeiotic segregation increased 2 pseudogene 8

PMS2P9 Gene

postmeiotic segregation increased 2 pseudogene 9

PMS2P2 Gene

postmeiotic segregation increased 2 pseudogene 2

PMS2P3 Gene

postmeiotic segregation increased 2 pseudogene 3

PMS2P4 Gene

postmeiotic segregation increased 2 pseudogene 4

PMS2P5 Gene

postmeiotic segregation increased 2 pseudogene 5

PMS2P6 Gene

postmeiotic segregation increased 2 pseudogene 6

PMS2P7 Gene

postmeiotic segregation increased 2 pseudogene 7

PMS1 Gene

PMS1 postmeiotic segregation increased 1 (S. cerevisiae)

This gene encodes a protein belonging to the DNA mismatch repair mutL/hexB family. This protein is thought to be involved in the repair of DNA mismatches, and it can form heterodimers with MLH1, a known DNA mismatch repair protein. Mutations in this gene cause hereditary nonpolyposis colorectal cancer type 3 (HNPCC3) either alone or in combination with mutations in other genes involved in the HNPCC phenotype, which is also known as Lynch syndrome. [provided by RefSeq, Jul 2008]

PMS2 Gene

PMS2 postmeiotic segregation increased 2 (S. cerevisiae)

This gene is one of the PMS2 gene family members found in clusters on chromosome 7. The product of this gene is involved in DNA mismatch repair. It forms a heterodimer with MLH1 and this complex interacts with other complexes bound to mismatched bases. Mutations in this gene are associated with hereditary nonpolyposis colorectal cancer, Turcot syndrome, and are a cause of supratentorial primitive neuroectodermal tumors. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Jul 2008]

PMS2P12 Gene

postmeiotic segregation increased 2 pseudogene 12

PMS2P1 Gene

postmeiotic segregation increased 2 pseudogene 1

LOC441259 Gene

postmeiotic segregation increased 2 pseudogene

PMS2P10 Gene

postmeiotic segregation increased 2 pseudogene 10

LOC391020 Gene

interferon induced transmembrane protein 3 pseudogene

SIPA1L1 Gene

signal-induced proliferation-associated 1 like 1

SIPA1L2 Gene

signal-induced proliferation-associated 1 like 2

SIPA1 Gene

signal-induced proliferation-associated 1

The product of this gene is a mitogen induced GTPase activating protein (GAP). It exhibits a specific GAP activity for Ras-related regulatory proteins Rap1 and Rap2, but not for Ran or other small GTPases. This protein may also hamper mitogen-induced cell cycle progression when abnormally or prematurely expressed. It is localized to the perinuclear region. Two alternatively spliced variants encoding the same isoform have been characterized to date. [provided by RefSeq, Jul 2008]

IFITM8P Gene

interferon induced transmembrane protein 8 pseudogene

IFI35 Gene

interferon-induced protein 35

IFIT1P1 Gene

interferon-induced protein with tetratricopeptide repeats 1 pseudogene 1

STIP1 Gene

stress-induced phosphoprotein 1

STIP1 is an adaptor protein that coordinates the functions of HSP70 (see HSPA1A; MIM 140550) and HSP90 (see HSP90AA1; MIM 140571) in protein folding. It is thought to assist in the transfer of proteins from HSP70 to HSP90 by binding both HSP90 and substrate-bound HSP70. STIP1 also stimulates the ATPase activity of HSP70 and inhibits the ATPase activity of HSP90, suggesting that it regulates both the conformations and ATPase cycles of these chaperones (Song and Masison, 2005 [PubMed 16100115]).[supplied by OMIM, Jul 2009]

PIH2 Gene

pregnancy-induced hypertension syndrome-related protein

PIP Gene

prolactin-induced protein

PIDD1 Gene

p53-induced death domain protein 1

The protein encoded by this gene contains a leucine-rich repeat and a death domain. This protein has been shown to interact with other death domain proteins, such as Fas (TNFRSF6)-associated via death domain (FADD) and MAP-kinase activating death domain-containing protein (MADD), and thus may function as an adaptor protein in cell death-related signaling processes. The expression of the mouse counterpart of this gene has been found to be positively regulated by the tumor suppressor p53 and to induce cell apoptosis in response to DNA damage, which suggests a role for this gene as an effector of p53-dependent apoptosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2010]

AICDA Gene

activation-induced cytidine deaminase

This gene encodes a RNA-editing deaminase that is a member of the cytidine deaminase family. The protein is involved in somatic hypermutation, gene conversion, and class-switch recombination of immunoglobulin genes. Defects in this gene are the cause of autosomal recessive hyper-IgM immunodeficiency syndrome type 2 (HIGM2). [provided by RefSeq, Feb 2009]

PMAIP1 Gene

phorbol-12-myristate-13-acetate-induced protein 1

GDAP2 Gene

ganglioside induced differentiation associated protein 2

GDAP1 Gene

ganglioside induced differentiation associated protein 1

This gene encodes a member of the ganglioside-induced differentiation-associated protein family, which may play a role in a signal transduction pathway during neuronal development. Mutations in this gene have been associated with various forms of Charcot-Marie-Tooth Disease and neuropathy. Two transcript variants encoding different isoforms and a noncoding variant have been identified for this gene. [provided by RefSeq, Feb 2012]

TGFB1I1 Gene

transforming growth factor beta 1 induced transcript 1

This gene encodes a coactivator of the androgen receptor, a transcription factor which is activated by androgen and has a key role in male sexual differentiation. The encoded protein is thought to regulate androgen receptor activity and may have a role to play in the treatment of prostate cancer. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

TNFAIP8L2 Gene

tumor necrosis factor, alpha-induced protein 8-like 2

TNFAIP8L1 Gene

tumor necrosis factor, alpha-induced protein 8-like 1

LOC442017 Gene

interferon induced transmembrane protein 3 pseudogene

IFITM5 Gene

interferon induced transmembrane protein 5

This gene encodes a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195). [provided by RefSeq, Aug 2012]

PINK1 Gene

PTEN induced putative kinase 1

This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease. [provided by RefSeq, Jul 2008]

MNRI Gene

meningioma, radiation-induced

IFI44 Gene

interferon-induced protein 44

PARTICL Gene

promoter of MAT2A antisense radiation-induced circulating long non-coding RNA

LSINCT5 Gene

long stress-induced non-coding transcript 5

TGIF2P1 Gene

TGFB-induced factor homeobox 2 pseudogene 1

AVPI1 Gene

arginine vasopressin-induced 1

PRINS Gene

psoriasis associated non-protein coding RNA induced by stress

STAT6 Gene

signal transducer and activator of transcription 6, interleukin-4 induced

The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein plays a central role in exerting IL4 mediated biological responses. It is found to induce the expression of BCL2L1/BCL-X(L), which is responsible for the anti-apoptotic activity of IL4. Knockout studies in mice suggested the roles of this gene in differentiation of T helper 2 (Th2) cells, expression of cell surface markers, and class switch of immunoglobulins. Alternative splicing results in multiple transcript variants.[provided by RefSeq, May 2010]

RAI1 Gene

retinoic acid induced 1

This gene is located within the Smith-Magenis syndrome region on chromosome 17. It is highly similar to its mouse counterpart and is expressed at high levels mainly in neuronal tissues. The protein encoded by this gene includes a polymorphic polyglutamine tract in the N-terminal domain. Expression of the mouse counterpart in neurons is induced by retinoic acid. This gene is associated with both the severity of the phenotype and the response to medication in schizophrenic patients. [provided by RefSeq, Jul 2008]

CIAPIN1P Gene

cytokine induced apoptosis inhibitor 1 pseudogene

SIPA1L3 Gene

signal-induced proliferation-associated 1 like 3

MINA Gene

MYC induced nuclear antigen

MINA is a c-Myc (MYC; MIM 190080) target gene that may play a role in cell proliferation or regulation of cell growth. (Tsuneoka et al., 2002 [PubMed 12091391]; Zhang et al., 2005 [PubMed 15897898]).[supplied by OMIM, May 2008]

EI24P2 Gene

etoposide induced 2.4 pseudogene 2

EI24P3 Gene

etoposide induced 2.4 pseudogene 3

EI24P1 Gene

etoposide induced 2.4 pseudogene 1

EI24P4 Gene

etoposide induced 2.4 pseudogene 4

IFIH1 Gene

interferon induced with helicase C domain 1

DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein that is upregulated in response to treatment with beta-interferon and a protein kinase C-activating compound, mezerein. Irreversible reprogramming of melanomas can be achieved by treatment with both these agents; treatment with either agent alone only achieves reversible differentiation. Genetic variation in this gene is associated with diabetes mellitus insulin-dependent type 19. [provided by RefSeq, Jul 2012]

PMEPA1 Gene

prostate transmembrane protein, androgen induced 1

This gene encodes a transmembrane protein that contains a Smad interacting motif (SIM). Expression of this gene is induced by androgens and transforming growth factor beta, and the encoded protein suppresses the androgen receptor and transforming growth factor beta signaling pathways though interactions with Smad proteins. Overexpression of this gene may play a role in multiple types of cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

TIGAR Gene

TP53 induced glycolysis regulatory phosphatase

This gene is regulated as part of the p53 tumor suppressor pathway and encodes a protein with sequence similarity to the bisphosphate domain of the glycolytic enzyme that degrades fructose-2,6-bisphosphate. The protein functions by blocking glycolysis and directing the pathway into the pentose phosphate shunt. Expression of this protein also protects cells from DNA damaging reactive oxygen species and provides some protection from DNA damage-induced apoptosis. The 12p13.32 region that includes this gene is paralogous to the 11q13.3 region. [provided by RefSeq, Jul 2008]

LOC100101247 Gene

interferon induced transmembrane protein pseudogene

LOC100101246 Gene

interferon induced transmembrane protein 3 pseudogene

LINC-PINT Gene

long intergenic non-protein coding RNA, p53 induced transcript

IFITM10 Gene

interferon induced transmembrane protein 10

LOC442389 Gene

interferon induced transmembrane protein pseudogene

RARRES2 Gene

retinoic acid receptor responder (tazarotene induced) 2

This gene encodes a secreted chemotactic protein that initiates chemotaxis via the ChemR23 G protein-coupled seven-transmembrane domain ligand. Expression of this gene is upregulated by the synthetic retinoid tazarotene and occurs in a wide variety of tissues. The active protein has several roles, including that as an adipokine and as an antimicrobial protein with activity against bacteria and fungi. [provided by RefSeq, Nov 2014]

RARRES3 Gene

retinoic acid receptor responder (tazarotene induced) 3

Retinoids exert biologic effects such as potent growth inhibitory and cell differentiation activities and are used in the treatment of hyperproliferative dermatological diseases. These effects are mediated by specific nuclear receptor proteins that are members of the steroid and thyroid hormone receptor superfamily of transcriptional regulators. RARRES1, RARRES2, and RARRES3 are genes whose expression is upregulated by the synthetic retinoid tazarotene. RARRES3 is thought act as a tumor suppressor or growth regulator. [provided by RefSeq, Jul 2008]

RARRES1 Gene

retinoic acid receptor responder (tazarotene induced) 1

This gene was identified as a retinoid acid (RA) receptor-responsive gene. It encodes a type 1 membrane protein. The expression of this gene is upregulated by tazarotene as well as by retinoic acid receptors. The expression of this gene is found to be downregulated in prostate cancer, which is caused by the methylation of its promoter and CpG island. Alternatively spliced transcript variant encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008]

EI24 Gene

etoposide induced 2.4

This gene encodes a putative tumor suppressor and has higher expression in p53-expressing cells than in control cells and is an immediate-early induction target of p53-mediated apoptosis. The encoded protein may suppress cell growth by inducing apoptotic cell death through the caspase 9 and mitochondrial pathways. This gene is located on human chromosome 11q24, a region frequently altered in cancers. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene have been defined on chromosomes 1, 3, 7, and 8. [provided by RefSeq, Feb 2014]

GDAP1L1 Gene

ganglioside induced differentiation associated protein 1-like 1

The ganglioside GD3 synthase causes cell differentiation with neurite sprouting when transfected into the mouse neuroblastoma cell line Neuro2a. After differentiation, the expression of several genes is upregulated, including one that encodes a protein termed ganglioside-induced differentiation-associated protein 1 (Gdap1). A similar gene was found in humans, and mutations in the human gene are associated with Charcot-Marie-Tooth type 4A disease. The protein encoded by this gene is similar in sequence to the human GDAP1 protein. Several transcript variants encoding different isoforms, as well as a noncoding transcript variant, have been found for this gene. [provided by RefSeq, Feb 2012]

IFITM9P Gene

interferon induced transmembrane protein 9 pseudogene

LOC442309 Gene

interferon induced transmembrane protein 3 pseudogene

LOC100187725 Gene

5-azacytidine induced 2 pseudogene

EBI3 Gene

Epstein-Barr virus induced 3

This gene was identified by its induced expression in B lymphocytes in response Epstein-Barr virus infection. It encodes a secreted glycoprotein belonging to the hematopoietin receptor family, and heterodimerizes with a 28 kDa protein to form interleukin 27 (IL-27). IL-27 regulates T cell and inflammatory responses, in part by activating the Jak/STAT pathway of CD4+ T cells. [provided by RefSeq, Sep 2008]

LOC728048 Gene

interferon induced transmembrane protein pseudogene

FGF8 Gene

fibroblast growth factor 8 (androgen-induced)

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth and invasion. This protein is known to be a factor that supports androgen and anchorage independent growth of mammary tumor cells. Overexpression of this gene has been shown to increase tumor growth and angiogensis. The adult expression of this gene is restricted to testes and ovaries. Temporal and spatial pattern of this gene expression suggests its function as an embryonic epithelial factor. Studies of the mouse and chick homologs revealed roles in midbrain and limb development, organogenesis, embryo gastrulation and left-right axis determination. The alternative splicing of this gene results in four transcript variants. [provided by RefSeq, Jul 2008]

ATRAID Gene

all-trans retinoic acid-induced differentiation factor

This gene is thought to be involved in apoptosis, and may also be involved in hematopoietic development and differentiation. The use of alternative splice sites and promotors result in multiple transcript variants encoding different isoforms.[provided by RefSeq, Dec 2009]

EPRPDC Gene

Epilepsy, rolandic, with paroxysmal exercise-induced dystonia and writer's cramp

OIT3 Gene

oncoprotein induced transcript 3

IFITM4P Gene

interferon induced transmembrane protein 4 pseudogene

INSIG1 Gene

insulin induced gene 1

Oxysterols regulate cholesterol homeostasis through the liver X receptor (LXR)- and sterol regulatory element-binding protein (SREBP)-mediated signaling pathways. This gene is an insulin-induced gene. It encodes an endoplasmic reticulum (ER) membrane protein that plays a critical role in regulating cholesterol concentrations in cells. This protein binds to the sterol-sensing domains of SREBP cleavage-activating protein (SCAP) and HMG CoA reductase, and is essential for the sterol-mediated trafficking of the two proteins. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jun 2009]

TNFAIP8 Gene

tumor necrosis factor, alpha-induced protein 8

LOC100533631 Gene

5-azacytidine induced 2 pseudogene

IFIT6P Gene

interferon-induced protein with tetratricopeptide repeats 6, pseudogene

TNFAIP6 Gene

tumor necrosis factor, alpha-induced protein 6

The protein encoded by this gene is a secretory protein that contains a hyaluronan-binding domain, and thus is a member of the hyaluronan-binding protein family. The hyaluronan-binding domain is known to be involved in extracellular matrix stability and cell migration. This protein has been shown to form a stable complex with inter-alpha-inhibitor (I alpha I), and thus enhance the serine protease inhibitory activity of I alpha I, which is important in the protease network associated with inflammation. This gene can be induced by proinflammatory cytokines such as tumor necrosis factor alpha and interleukin-1. Enhanced levels of this protein are found in the synovial fluid of patients with osteoarthritis and rheumatoid arthritis.[provided by RefSeq, Dec 2010]

TNFAIP1 Gene

tumor necrosis factor, alpha-induced protein 1 (endothelial)

This gene was identified as a gene whose expression can be induced by the tumor necrosis factor alpha (TNF) in umbilical vein endothelial cells. Studies of a similar gene in mouse suggest that the expression of this gene is developmentally regulated in a tissue-specific manner. [provided by RefSeq, Jul 2008]

TNFAIP3 Gene

tumor necrosis factor, alpha-induced protein 3

This gene was identified as a gene whose expression is rapidly induced by the tumor necrosis factor (TNF). The protein encoded by this gene is a zinc finger protein and ubiqitin-editing enzyme, and has been shown to inhibit NF-kappa B activation as well as TNF-mediated apoptosis. The encoded protein, which has both ubiquitin ligase and deubiquitinase activities, is involved in the cytokine-mediated immune and inflammatory responses. Several transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jul 2012]

TNFAIP2 Gene

tumor necrosis factor, alpha-induced protein 2

This gene was identified as a gene whose expression can be induced by the tumor necrosis factor alpha (TNF) in umbilical vein endothelial cells. The expression of this gene was shown to be induced by retinoic acid in a cell line expressing a oncogenic version of the retinoic acid receptor alpha fusion protein, which suggested that this gene may be a retinoic acid target gene in acute promyelocytic leukemia. [provided by RefSeq, Jul 2008]

TGFBI Gene

transforming growth factor, beta-induced, 68kDa

This gene encodes an RGD-containing protein that binds to type I, II and IV collagens. The RGD motif is found in many extracellular matrix proteins modulating cell adhesion and serves as a ligand recognition sequence for several integrins. This protein plays a role in cell-collagen interactions and may be involved in endochondrial bone formation in cartilage. The protein is induced by transforming growth factor-beta and acts to inhibit cell adhesion. Mutations in this gene are associated with multiple types of corneal dystrophy. [provided by RefSeq, Jul 2008]

TGIF1P1 Gene

TGFB-induced factor homeobox 1 pseudogene 1

DSPA2D Gene

interferon induced transmembrane protein 3 pseudogene

LITAF Gene

lipopolysaccharide-induced TNF factor

Lipopolysaccharide is a potent stimulator of monocytes and macrophages, causing secretion of tumor necrosis factor-alpha (TNF-alpha) and other inflammatory mediators. This gene encodes lipopolysaccharide-induced TNF-alpha factor, which is a DNA-binding protein and can mediate the TNF-alpha expression by direct binding to the promoter region of the TNF-alpha gene. The transcription of this gene is induced by tumor suppressor p53 and has been implicated in the p53-induced apoptotic pathway. Mutations in this gene cause Charcot-Marie-Tooth disease type 1C (CMT1C) and may be involved in the carcinogenesis of extramammary Paget's disease (EMPD). Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2014]

PERM1 Gene

PPARGC1 and ESRR induced regulator, muscle 1

IFI44L Gene

interferon-induced protein 44-like

TGIF2LY Gene

TGFB-induced factor homeobox 2-like, Y-linked

This gene encodes a member of the TALE/TGIF homeobox family of transcription factors. This gene lies within the male specific region of chromosome Y, in a block of sequence that is thought to be the result of a large X-to-Y transposition. The C-terminus of this protein is divergent from that of its chromosome X homolog (TGIF2LX), suggesting that this protein may act as a regulator of TGIF2LX. [provided by RefSeq, Jul 2008]

TGIF2LX Gene

TGFB-induced factor homeobox 2-like, X-linked

This gene encodes a member of the TALE/TGIF homeobox family of transcription factors. Testis-specific expression suggests that this gene may play a role in spermatogenesis. A homolog of this gene lies within the male specific region of chromosome Y, in a block of sequence that is thought to be the result of a large X-to-Y transposition. [provided by RefSeq, Jul 2008]

OSGIN2 Gene

oxidative stress induced growth inhibitor family member 2

OSGIN1 Gene

oxidative stress induced growth inhibitor 1

This gene encodes an oxidative stress response protein that regulates cell death. Expression of the gene is regulated by p53 and is induced by DNA damage. The protein regulates apoptosis by inducing cytochrome c release from mitochondria. It also appears to be a key regulator of both inflammatory and anti-inflammatory molecules. The loss of this protein correlates with uncontrolled cell growth and tumor formation. Naturally occurring read-through transcription exists between this gene and the neighboring upstream malonyl-CoA decarboxylase (MLYCD) gene, but the read-through transcripts are unlikely to produce a protein product. [provided by RefSeq, Aug 2011]

AIG1 Gene

androgen-induced 1

BREA2 Gene

breast cancer estrogen-induced apoptosis 2

RAI2 Gene

retinoic acid induced 2

Retinoic acid plays a critical role in development, cellular growth, and differentiation. The specific function of this retinoic acid-induced gene has not yet been determined but it may play a role in development. The chromosomal location of this gene designates it to be a candidate for diseases such as Nance-Horan syndrome, sensorineural deafness, non-specific X-linked mental retardation, oral-facial-digital syndrome, and Fried syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Feb 2010]

IFITM3 Gene

interferon induced transmembrane protein 3

The protein encoded by this gene is an interferon-induced membrane protein that helps confer immunity to influenza A H1N1 virus, West Nile virus, and dengue virus. Two transcript variants, only one of them protein-coding, have been found for this gene. Another variant encoding an N-terminally truncated isoform has been reported, but the full-length nature of this variant has not been determined. [provided by RefSeq, May 2012]

IFITM1 Gene

interferon induced transmembrane protein 1

GLCCI1 Gene

glucocorticoid induced 1

This gene encodes a protein of unknown function. Expression of this gene is induced by glucocorticoids and may be an early marker for glucocorticoid-induced apoptosis. Single nucleotide polymorphisms in this gene are associated with a decreased response to inhaled glucocorticoids in asthmatic patients. [provided by RefSeq, Feb 2012]

IL4I1 Gene

interleukin 4 induced 1

This gene encodes a protein with limited similarity to L-amino acid oxidase which contains the conserved amino acids thought to be involved in catalysis and binding of flavin adenine dinucleotide (FAD) cofactor. The expression of this gene can be induced by interleukin 4 in B cells, however, expression of transcripts containing the first two exons of the upstream gene is found in other cell types. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2012]

LOC123862 Gene

interferon induced transmembrane protein pseudogene

LOC101929989 Gene

lipopolysaccharide-induced tumor necrosis factor-alpha factor-like

RARRES2P8 Gene

retinoic acid receptor responder (tazarotene induced) 2 pseudogene 8

RARRES2P2 Gene

retinoic acid receptor responder (tazarotene induced) 2 pseudogene 2

RARRES2P1 Gene

retinoic acid receptor responder (tazarotene induced) 2 pseudogene 1

RARRES2P4 Gene

retinoic acid receptor responder (tazarotene induced) 2 pseudogene 4

IFITM2 Gene

interferon induced transmembrane protein 2

AZI2 Gene

5-azacytidine induced 2

AZI2, or NAP1, contributes to the activation of NFKB (see MIM 164011)-dependent gene expression by activating IKK-related kinases, such as NAK (TBK1; MIM 604834) (Fujita et al., 2003 [PubMed 14560022]).[supplied by OMIM, Mar 2008]

TIAF1 Gene

TGFB1-induced anti-apoptotic factor 1

IFIT5 Gene

interferon-induced protein with tetratricopeptide repeats 5

IFIT3 Gene

interferon-induced protein with tetratricopeptide repeats 3

IFIT2 Gene

interferon-induced protein with tetratricopeptide repeats 2

IFIT1 Gene

interferon-induced protein with tetratricopeptide repeats 1

This gene encodes a protein containing tetratricopeptide repeats that was originally identified as induced upon treatment with interferon. The encoded protein may inhibit viral replication and translational initiation. This gene is located in a cluster on chromosome 10 with five other closely related genes. There is a pseudogene for this gene on chromosome 13. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Aug 2012]

FIGF Gene

c-fos induced growth factor (vascular endothelial growth factor D)

The protein encoded by this gene is a member of the platelet-derived growth factor/vascular endothelial growth factor (PDGF/VEGF) family and is active in angiogenesis, lymphangiogenesis, and endothelial cell growth. This secreted protein undergoes a complex proteolytic maturation, generating multiple processed forms which bind and activate VEGFR-2 and VEGFR-3 receptors. This protein is structurally and functionally similar to vascular endothelial growth factor C. Read-through transcription has been observed between this locus and the upstream PIR (GeneID 8544) locus. [provided by RefSeq, Feb 2011]

LOC390600 Gene

cytokine induced apoptosis inhibitor 1 pseudogene

CIAPIN1 Gene

cytokine induced apoptosis inhibitor 1

CIAPIN1 is a cytokine-induced inhibitor of apoptosis with no relation to apoptosis regulatory molecules of the BCL2 (MIM 151430) or CASP (see MIM 147678) families. Expression of CIAPIN1 is dependent on growth factor stimulation (Shibayama et al., 2004 [PubMed 14970183]).[supplied by OMIM, Mar 2008]

STIP1P1 Gene

stress-induced phosphoprotein 1 pseudogene 1

STIP1P2 Gene

stress-induced phosphoprotein 1 pseudogene 2

STIP1P3 Gene

stress-induced phosphoprotein 1 pseudogene 3

LOC643058 Gene

interferon induced transmembrane protein 3 pseudogene

TNFAIP8L3 Gene

tumor necrosis factor, alpha-induced protein 8-like 3

EI24P5 Gene

etoposide induced 2.4 pseudogene 5

RAI14 Gene

retinoic acid induced 14

INSIG2 Gene

insulin induced gene 2

The protein encoded by this gene is highly similar to the protein product encoded by gene INSIG1. Both INSIG1 protein and this protein are endoplasmic reticulum proteins that block the processing of sterol regulatory element binding proteins (SREBPs) by binding to SREBP cleavage-activating protein (SCAP), and thus prevent SCAP from escorting SREBPs to the Golgi. [provided by RefSeq, Jul 2008]

RASD1 Gene

RAS, dexamethasone-induced 1

This gene encodes a member of the Ras superfamily of small GTPases and is induced by dexamethasone. The encoded protein is an activator of G-protein signaling and acts as a direct nucleotide exchange factor for Gi-Go proteins. This protein interacts with the neuronal nitric oxide adaptor protein CAPON, and a nuclear adaptor protein FE65, which interacts with the Alzheimer's disease amyloid precursor protein. This gene may play a role in dexamethasone-induced alterations in cell morphology, growth and cell-extracellular matrix interactions. Epigenetic inactivation of this gene is closely correlated with resistance to dexamethasone in multiple myeloma cells. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2011]

DDIAS Gene

DNA damage-induced apoptosis suppressor

IFIT1B Gene

interferon-induced protein with tetratricopeptide repeats 1B

LOC100129830 Gene

5-azacytidine induced 2 pseudogene

TGIF2 Gene

TGFB-induced factor homeobox 2

The protein encoded by this gene is a DNA-binding homeobox protein and a transcriptional repressor, which appears to repress transcription by recruiting histone deacetylases to TGF beta-responsive genes. This gene is amplified and over-expressed in some ovarian cancers. Alternative splicing results in multiple transcript variants. A related pseudogene has been identified on chromosome 1. Read-through transcription also exists between this gene and the neighboring downstream C20orf24 (chromosome 20 open reading frame 24) gene. [provided by RefSeq, Dec 2010]

TGIF1 Gene

TGFB-induced factor homeobox 1

The protein encoded by this gene is a member of the three-amino acid loop extension (TALE) superclass of atypical homeodomains. TALE homeobox proteins are highly conserved transcription regulators. This particular homeodomain binds to a previously characterized retinoid X receptor responsive element from the cellular retinol-binding protein II promoter. In addition to its role in inhibiting 9-cis-retinoic acid-dependent RXR alpha transcription activation of the retinoic acid responsive element, the protein is an active transcriptional co-repressor of SMAD2 and may participate in the transmission of nuclear signals during development and in the adult. Mutations in this gene are associated with holoprosencephaly type 4, which is a structural anomaly of the brain. Alternative splicing has been observed at this locus and multiple splice variants encoding distinct isoforms are described. [provided by RefSeq, Jul 2013]

BMIQ7 Gene

Obesity, susceptibility to, on chromosome 4

ASPG2 Gene

Asperger syndrome, susceptibility to, 2

ASPG3 Gene

Asperger syndrome, susceptibility to, 3

ASPG4 Gene

Asperger syndrome, susceptibility to, 4

ATOD7 Gene

Dermatitis, atopic, susceptibility to, 7

ENDO1 Gene

Endometriosis, susceptibility to, 1

HYT3 Gene

Hypertension, essential, susceptibility to, 3

HYT5 Gene

Hypertension, essential, susceptibility to, 5

HYT4 Gene

Hypertension, essential, susceptibility to, 4

HYT7 Gene

Hypertension, essential, susceptibility to, 7

HYT6 Gene

Hypertension, essential, susceptibility to, 6

HYT8 Gene

hypertension, essential, susceptibility to, 8

MGR7 Gene

Migraine with aura, susceptibility to, 7

MGR9 Gene

Migraine with aura, susceptibility to, 9

GRD2 Gene

Graves disease, susceptibility to, 2

GRDX Gene

Graves disease, susceptibility to, X-linked

EIG4 Gene

Epilepsy, idiopathic generalized, susceptibility to 4

PRAC2 Gene

prostate cancer susceptibility candidate 2

This gene is highly expressed in prostate, rectum, colon, and testis. This gene may produce a non-coding RNA or may encode a short protein that might localize to the nucleus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]

PRAC1 Gene

prostate cancer susceptibility candidate 1

This gene is reported to be specifically expressed in prostate, rectum and distal colon. Sequence analysis suggests that it may play a regulatory role in the nucleus. [provided by RefSeq, Jul 2008]

SS3 Gene

Sarcoidosis, susceptibility to, 3

BMIQ10 Gene

Obesity, susceptibility to, on chromosome 10q

PSORS9 Gene

psoriasis susceptibility 9

PSORS8 Gene

psoriasis susceptibility 8

PSORS7 Gene

psoriasis susceptibility 7

PSORS6 Gene

psoriasis susceptibility 6

PSORS5 Gene

psoriasis susceptibility 5

PSORS4 Gene

psoriasis susceptibility 4

PSORS3 Gene

psoriasis susceptibility 3

NKS1 Gene

natural killer cell susceptibility 1

CELIAC8 Gene

Celiac disease, susceptibility to, 8

CELIAC5 Gene

Celiac disease, susceptibility to, 5

CELIAC6 Gene

Celiac disease, susceptibility to, 6

CELIAC7 Gene

Celiac disease, susceptibility to, 7

AIS3 Gene

autoimmune susceptibility 3 (vitiligo specific)

AIS2 Gene

autoimmune susceptibility 2

AIS1 Gene

autoimmune susceptibility 1

AIS4 Gene

autoimmune disease, susceptibility to, 4

SLEB13 Gene

Systemic lupus erythematosus, susceptibility to, 13

SLEB12 Gene

Systemic lupus erythematosus, susceptibility to, 12

SLEB15 Gene

Systemic lupus erthematosus, susceptibility to, 15

IGAD1 Gene

immunoglobulin A (IgA) deficiency susceptibility 1

OS4 Gene

Osteoarthritis, generalized, without dysplasia, susceptibility to

OS6 Gene

Osteoarthritis susceptibility 6

CASC4P1 Gene

cancer susceptibility candidate 4 pseudogene 1

BCC5 Gene

Basal cell carcinoma, susceptibility to, 5

NBLST5 Gene

Neuroblastoma, susceptibility to, 5

NBLST4 Gene

Neuroblastoma, susceptibility to, 4

NBLST6 Gene

Neuroblastoma, susceptibility to, 6

MAFD9 Gene

Major affective disorder-9, susceptibility to

MAFD8 Gene

Major affective disorder-8, susceptibility to

IGAN2 Gene

IgA nephropathy, susceptibility to, 2

AUTS6 Gene

Autism, susceptibility to, 6

AUTS7 Gene

Autism, susceptibility to, 7

AUTS5 Gene

Autism, susceptibility to, 5

AUTS2 Gene

autism susceptibility candidate 2

This gene has been implicated in neurodevelopment and as a candidate gene for numerous neurological disorders, including autism spectrum disorders, intellectual disability, and developmental delay. Mutations in this gene have also been associated with non-neurological disorders, such as acute lymphoblastic leukemia, aging of the skin, early-onset androgenetic alopecia, and certain cancers. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, May 2014]

AUTS3 Gene

Autism, susceptibility to, 3

AUTS1 Gene

Autism, susceptibility to, 1

AUTS8 Gene

Autism, susceptibility to, 8

EIG3 Gene

Epilepsy, idiopathic generalized, susceptibility to 3

EIG2 Gene

Epilepsy, idiopathic generalized, susceptibility to 2

CASC2 Gene

cancer susceptibility candidate 2 (non-protein coding)

CASC1 Gene

cancer susceptibility candidate 1

CASC6 Gene

cancer susceptibility candidate 6 (non-protein coding)

CASC5 Gene

cancer susceptibility candidate 5

The protein encoded by this gene is a component of the multiprotein assembly that is required for creation of kinetochore-microtubule attachments and chromosome segregation. The encoded protein functions as a scaffold for proteins that influence the spindle assembly checkpoint during the eukaryotic cell cycle and it interacts with at least five different kinetochore proteins and two checkpoint kinases. In adults, this gene is predominantly expressed in normal testes, various cancer cell lines and primary tumors from other tissues and is ubiquitously expressed in fetal tissues. This gene was originally identified as a fusion partner with the mixed-lineage leukemia (MLL) gene in t(11;15)(q23;q14). Mutations in this gene cause autosomal recessive primary microcephaly-4 (MCPH4). Alternative splicing results in multiple transcript variants encoding different isoforms. Additional splice variants have been described but their biological validity has not been confirmed. [provided by RefSeq, Jan 2013]

CASC4 Gene

cancer susceptibility candidate 4

The increased expression level of this gene is associated with HER-2/neu proto-oncogene overexpression. Amplification and resulting overexpression of this proto-oncogene are found in approximately 30% of human breast and 20% of human ovarian cancers. Alternatively spliced variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Dec 2010]

CASC8 Gene

cancer susceptibility candidate 8 (non-protein coding)

HYT1 Gene

Hypertension, essential, susceptibility to, 1

HYT2 Gene

Hypertension, essential, susceptibility to, 2

BCC6 Gene

Basal cell carcinoma, susceptibility to, 6

CASC18 Gene

cancer susceptibility candidate 18 (non-protein coding)

ADHD2 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

CLLS1 Gene

Leukemia, chronic lymphocytic, susceptibility to, 1

LOC101930332 Gene

autism susceptibility gene 2 protein-like

ASRT8 Gene

Asthma-related traits, susceptibility to, 8

OVCAS1 Gene

Ovarian cancer, epithelial, susceptibility to

OMS Gene

otitis media, susceptibility to

EIG5 Gene

Epilepsy, idiopathic generalized, susceptibility to, 5

KAZA1 Gene

Kala-azar (visceral leishmaniasis), susceptibility to

KAZA2 Gene

Kala-azar, susceptibility to, 2

KAZA3 Gene

Kala-azar, susceptibility to, 3

DYX5 Gene

dyslexia susceptibility 5

PSORS1C1 Gene

psoriasis susceptibility 1 candidate 1

This gene is one of several genes thought to confer susceptibility to psoriasis and systemic sclerosis, located on chromosome 6 near the major histocompatibility complex (MHC) class I region. [provided by RefSeq, Sep 2011]

PSORS1C3 Gene

psoriasis susceptibility 1 candidate 3 (non-protein coding)

PSORS1C2 Gene

psoriasis susceptibility 1 candidate 2

AUTS11 Gene

Autism, susceptibility to, 11

AUTS12 Gene

autism, susceptibility to, 12

AUTS13 Gene

autism, susceptibility to, 13

HPC6 Gene

Prostate cancer, susceptibility to

MTBS3 Gene

Mycobacterium tuberculosis, susceptibility to, 3

MTBS2 Gene

Mycobacterium tuberculosis, susceptibility to, 2

MTBS1 Gene

mycobacterium tuberculosis, susceptibility to infection by, 1

MTBSX Gene

Mycobacterium tuberculosis, susceptibility to infection by

CASC3 Gene

cancer susceptibility candidate 3

The product of this gene is a core component of the exon junction complex (EJC), a protein complex that is deposited on spliced mRNAs at exon-exon junctions and functions in nonsense-mediated mRNA decay (NMD). The encoded protein binds RNA and interacts with two other EJC core components. It is predominantly located in the cytoplasm, but shuttles into the nucleus where it localizes to nuclear speckles. [provided by RefSeq, Jul 2008]

CASC7 Gene

cancer susceptibility candidate 7 (non-protein coding)

CASC9 Gene

cancer susceptibility candidate 9 (non-protein coding)

CHDS4 Gene

Coronary heart disease, susceptibility to, 4

CLLS3 Gene

Leukemia, chronic lymphocytic, susceptibility to, 3

CASC11 Gene

cancer susceptibility candidate 11 (non-protein coding)

CASC10 Gene

cancer susceptibility candidate 10

CASC17 Gene

cancer susceptibility candidate 17 (non-protein coding)

CASC16 Gene

cancer susceptibility candidate 16 (non-protein coding)

CASC15 Gene

cancer susceptibility candidate 15 (non-protein coding)

CASC19 Gene

cancer susceptibility candidate 19 (non-protein coding)

ADHD4 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 4

ADHD5 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 5

ADHD6 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 6

ADHD1 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 1

ADHD3 Gene

Attention deficit-hyperactivity disorder, susceptibility to, 2

ASOBS Gene

Asthma and obesity susceptibility, chromosome 16p11 inversion related

BULN Gene

Bulimia nervosa, susceptibility to

ALL2 Gene

Leukemia, acute lymphoblastic, susceptibility to, 2

GLM6 Gene

Glioma susceptibility 6

GLM7 Gene

Glioma susceptibility 7

GLM5 Gene

Glioma susceptibility 5

GLM8 Gene

Glioma susceptibility 8

STBMS1 Gene

Strabismus, susceptibility to, 1

IS5 Gene

scoliosis, idiopathic, susceptibility to, 5

IS4 Gene

Scoliosis, idiopathic, susceptibility to, 4

CRCS10 Gene

Colorectal cancer, susceptibility to, 10

CRCS11 Gene

Colorectal cancer, susceptibility to, 11

NPCA2 Gene

Nasopharyngeal carcinoma, susceptibility to, 2

SM2 Gene

Hepatic fibrosis susceptibility due to Schistosoma mansoni infection

SM1 Gene

Schistosoma mansoni, susceptibility/resistance to

PDCOS Gene

Podoconiosis, susceptibility to

CTEPH1 Gene

Pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to

DEL16P11.2 Gene

autism, susceptibility to, 14

BTS1 Gene

bladder tumor susceptibility 1

PTCSC1 Gene

papillary thyroid carcinoma susceptibility candidate 1 (non-protein coding)

PTCSC3 Gene

papillary thyroid carcinoma susceptibility candidate 3 (non-protein coding)

CASC23 Gene

cancer susceptibility candidate 23 (non-protein coding)

CASC22 Gene

cancer susceptibility candidate 22 (non-protein coding)

CASC20 Gene

cancer susceptibility candidate 20 (non-protein coding)

CASC21 Gene

cancer susceptibility candidate 21 (non-protein coding)

CRCS8 Gene

Colorectal cancer, susceptibility to, 8

CRCS9 Gene

colorectal cancer, susceptibility to, 9

CRCS2 Gene

Colorectal cancer, susceptibility to, 2

CRCS5 Gene

Colorectal cancer, susceptibility to, 5

MBNP Gene

?Membranous nephropathy, susceptibility to

NAFLD2 Gene

Fatty liver disease, nonalcoholic, susceptibility to, 2

ANON1 Gene

Anorexia nervosa, susceptibility to, 1

BCC4 Gene

Basal cell carcinoma, susceptibility to, 4

CMM7 Gene

Melanoma, cutaneous malignant, susceptibility to, 7

LNCR3 Gene

Lung cancer susceptibility 3

LNCR4 Gene

Lung cancer susceptibility 4

LNCR5 Gene

Lung cancer susceptibility 5

CLLS4 Gene

Leukemia, chronic lymphocytic susceptibility to, 4

AITD2 Gene

Autoimmune thyroid disease, susceptibility to, 2

AITD1 Gene

Autoimmune thyroid disease, susceptibility to, 1

AITD4 Gene

Autoimmune thyroid disease, susceptibility to, 4

ASRT6 Gene

Asthma-related traits, susceptibility to, 6

ASRT4 Gene

Asthma-related traits, susceptibility to, 4

MS3 Gene

Multiple sclerosis, susceptibility to, 3

MS2 Gene

Multiple sclerosis, susceptibility to, 2

DYX9 Gene

dyslexia susceptibility 9

DYX8 Gene

dyslexia susceptibility 8

MHS6 Gene

malignant hyperthermia susceptibility 6

MHS4 Gene

malignant hyperthermia susceptibility 4

MHS2 Gene

malignant hyperthermia susceptibility 2

MHS3 Gene

Malignant hyperthermia susceptibility 3

MGR2 Gene

Migraine, familial typical, susceptibility to

MGR3 Gene

Migraine, familial, with or without aura, susceptibility to

MGR1 Gene

Migraine with aura, susceptibility to

MGR5 Gene

Migraine with or without aura, susceptibility to, 5

MGR8 Gene

Migraine, susceptibility to, 8

TSG101 Gene

tumor susceptibility 101

The protein encoded by this gene belongs to a group of apparently inactive homologs of ubiquitin-conjugating enzymes. The gene product contains a coiled-coil domain that interacts with stathmin, a cytosolic phosphoprotein implicated in tumorigenesis. The protein may play a role in cell growth and differentiation and act as a negative growth regulator. In vitro steady-state expression of this tumor susceptibility gene appears to be important for maintenance of genomic stability and cell cycle regulation. Mutations and alternative splicing in this gene occur in high frequency in breast cancer and suggest that defects occur during breast cancer tumorigenesis and/or progression. [provided by RefSeq, Jul 2008]

HDPA Gene

Hodgkin disease, susceptibility, pseudoautosomal

ASPG1 Gene

Asperger syndrome, susceptibility to, 1

SCZD14 Gene

schizophrenia, susceptibility to, 14

SCZD11 Gene

Schizophrenia susceptibility locus, chromosome 10q-related

LOC100288160 Gene

esophagus cancer-related gene-2 interaction susceptibility protein

BCC1 Gene

Basal cell carcinoma, susceptibility to, 1

BCC2 Gene

Basal cell carcinoma, susceptibility to, 2

BCC3 Gene

Basal cell carcinoma, susceptibility to, 3

ODS1 Gene

Opioid dependence, susceptibility to, 1

PARK16 Gene

Parkinson disease 16 (susceptibility)

PARK10 Gene

Parkinson disease 10 (susceptibility)

PARK12 Gene

Parkinson disease 12 (susceptibility)

PDA1 Gene

Patent ductus arteriosus, susceptibility to

LPRS Gene

Leprosy, susceptibility to 1

CRCS6 Gene

colorectal cancer, susceptibility to, 6

MMS Gene

Malignant mesothelioma, susceptibility to

DYX1C1 Gene

dyslexia susceptibility 1 candidate 1

This gene encodes a tetratricopeptide repeat domain-containing protein. The encoded protein interacts with estrogen receptors and the heat shock proteins, Hsp70 and Hsp90. An homologous protein in rat has been shown to function in neuronal migration in the developing neocortex. A chromosomal translocation involving this gene is associated with a susceptibility to developmental dyslexia. Mutations in this gene are associated with deficits in reading and spelling. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream cell cycle progression 1 (CCPG1) gene. [provided by RefSeq, Mar 2011]

MGR4 Gene

Migraine, susceptibility to, 4

HSCR9 Gene

Hirschsprung disease, susceptibility to, 9

HSCR5 Gene

Hirschsprung disease, susceptibility to, 5

The disorder described by Hirschsprung (1888) and known as Hirschsprung disease or aganglionic megacolon is characterized by congenital absence of intrinsic ganglion cells in the myenteric (Auerbach) and submucosal (Meissner) plexuses of the gastrointestinal tract. Patients are diagnosed with the short-segment form (S-HSCR, approximately 80% of cases) when the aganglionic segment does not extend beyond the upper sigmoid, and with the long-segment form (L-HSCR) when aganglionosis extends proximal to the sigmoid. Total colonic aganglionosis and total intestinal HSCR also occur (Amiel et al., 2008 [PubMed 17965226]). Isolated HSCR appears to be of complex nonmendelian inheritance with low sex-dependent penetrance and variable expression according to the length of the aganglionic segment, suggestive of the involvement of one or more genes with low penetrance (Amiel et al., 2008 [PubMed 17965226]). For a general description and a discussion of genetic heterogeneity of Hirschsprung disease (HSCR), see MIM 142623.[supplied by OMIM, Feb 2011]

PTCSC2 Gene

papillary thyroid carcinoma susceptibility candidate 2 (non-protein coding)

DYX1 Gene

dyslexia susceptibility 1

DYX3 Gene

dyslexia susceptibility 3

DYX4 Gene

dyslexia susceptibility 4

DYX7 Gene

dyslexia susceptibility 7

DYX6 Gene

dyslexia susceptibility 6

FL1 Gene

Follicular lymphoma, susceptibility to, 1

TGCT1 Gene

testicular germ cell tumor susceptibility 1

DELXP22.11 Gene

Autism, X-linked, susceptibility to, 4

ASRT3 Gene

Asthma-related traits, susceptibility to, 3

RLS1 Gene

Restless legs syndrome, susceptibility to

RLS6 Gene

Restless legs syndrome, susceptibility to, 6

RLS5 Gene

Restless legs syndrome, susceptibility to, 5

RLS8 Gene

Restless legs syndrome, susceptibility to, 8

CELIAC9 Gene

Celiac disease, susceptibility to, 9

ALL1 Gene

Leukemia, acute lymphocytic, susceptibility to, 1

LOAS Gene

Leber optic atrophy, susceptibility to

SLEB4 Gene

systemic lupus erythematosus, susceptibility to, 4

UVM2 Gene

Melanoma, uveal, susceptibility to, 2

UVM1 Gene

Melanoma, uveal, susceptibility to, 1

ARMS2 Gene

age-related maculopathy susceptibility 2

This gene encodes a protein that is thought to play a role in diseases in the elderly. Mutations in this gene have been associated with age-related macular degeneration. [provided by RefSeq, Oct 2008]

ATHS Gene

atherosclerosis susceptibility (lipoprotein associated)

WM2 Gene

Macroglobulinemia, Waldenstrom, susceptibility to, 2

CMTS Gene

Chronic mountain sickness, susceptibility to

CHDS3 Gene

Coronary heart disease, susceptibility to, 3

CHDS2 Gene

Coronary heart disease, susceptibility to, 2

CHDS1 Gene

Coronary heart disease, susceptibility to, 1

CHDS8 Gene

Coronary heart disease, susceptibility to, 8

HHV8S Gene

Human herpesvirus 8, susceptibility to

IDDMX Gene

Diabetes mellitus, insulin-dependent, X-linked, susceptibility to

SLEB5 Gene

Systemic lupus erythematosus, susceptibility to, 5

SLEB8 Gene

Systemic lupus erythematosus, susceptibility to, 8

PSORS11 Gene

Psoriasis susceptibility 11

PSORS10 Gene

psoriasis susceptibility 10

SPDA3 Gene

Spondylarthropathy, susceptibility to, 3

SPDA2 Gene

Spondyloarthropathy, susceptibility to, 2

MGR12 Gene

Migraine, with or without aura, susceptibility to, 12

WM1 Gene

Macroglobulinemia, Waldenstrom, susceptibility to, 1

CRCS7 Gene

colorectal cancer, susceptibility to, 7

CELIAC12 Gene

Celiac disease, susceptibility to, 12

CELIAC13 Gene

Celiac disease, susceptibility to, 13

CELIAC10 Gene

Celiac disease, susceptibility to, 10

CELIAC11 Gene

Celiac disease, susceptibility to, 11

PVOP1 Gene

Pelvic organ prolapse, susceptibility to, 1

PVOP2 Gene

Pelvic organ prolapse, susceptibility to, 2

SLEB3 Gene

systemic lupus erythematosus susceptibility 3

SLEB7 Gene

Systemic lupus erythematosus, susceptibility to, 7

increased susceptibility to ototoxicity-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to ototoxicity-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; hearing loss, bilateral; hearing loss, sensorineural; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

complete hearing loss; deafness; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hearing loss, sudden; sensorineural hearing loss; vascular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing impairment; hearing loss; hearing loss, noise-induced; occupational diseases 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.

complete hearing loss; deafness; hearing impairment; hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; hearing impairment; hearing loss 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.

increased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hearing loss; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; sensorineural hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

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

complete hearing loss; deafness; hearing loss, bilateral Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; hemoglobin sc disease; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; learning disorders; melas syndrome; migraine disorders; mitochondrial diseases; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; hearing loss, sensorineural; hearing loss, sudden; thrombosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, bilateral; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

deafness; hearing loss; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; hypercholesterolemia; hyperhomocysteinemia; sensorineural hearing loss; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

cytomegalovirus infections; hearing loss, sensorineural; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease apraxias; hearing loss, sensorineural; language development disorders; mutism; sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, sensorineural; keratoderma, palmoplantar; palmoplantar keratosis; sensorineural hearing loss; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO from the curated CTD Gene-Disease Associations dataset.

decreased susceptibility to noise-induced hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to noise-induced hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{?hearing loss, cisplatin-induced, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {?hearing loss, cisplatin-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

increased susceptibility to age-related hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to age-related hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hearing impairment; hearing loss; otosclerosis Gene Set

From GAD Gene-Disease Associations

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

hearing impairment; hearing loss; infant, premature, diseases Gene Set

From GAD Gene-Disease Associations

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

genetic diseases, inborn; hearing impairment; hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing impairment; hearing loss; neoplasms, testis; testicular neoplasms Gene Set

From GAD Gene-Disease Associations

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

hearing impairment; hearing loss Gene Set

From GAD Gene-Disease Associations

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

eye diseases, hereditary; hearing impairment; hearing loss; hereditary nephritis; nephritis, hereditary Gene Set

From GAD Gene-Disease Associations

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

Hearing Loss, Noise-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hearing Loss, Noise-Induced from the curated CTD Gene-Disease Associations dataset.

hearing loss, noise-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss, noise-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, noise-induced Gene Set

From GAD Gene-Disease Associations

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

Hearing Loss, Noise-Induced Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

alveolar bone loss; periodontal attachment loss; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormal susceptibility to hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; dental plaque; disease susceptibility; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

ototoxicity Gene Set

From GAD Gene-Disease Associations

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

ototoxicity Gene Set

From GeneRIF Biological Term Annotations

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

increased susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

diabetes mellitus type ii; diabetes mellitus, type 2; hearing disorders; hearing problem Gene Set

From GAD Gene-Disease Associations

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

hearing disorders; hearing problem; syndrome Gene Set

From GAD Gene-Disease Associations

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

hearing disorders; hearing problem Gene Set

From GAD Gene-Disease Associations

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

diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease diabetes mellitus; hearing disorders; hearing problem; mitochondrial diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

increased susceptibility to induced choroid neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced choroid neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to bacterial infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced colitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced colitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to viral infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to parasitic infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to pharmacologically induced seizures Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced pancreatitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced pancreatitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induced arthritis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induced arthritis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to diet-induced obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to diet-induced obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

DFNA 2 Nonsyndromic Hearing Loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the DFNA 2 Nonsyndromic Hearing Loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Camptodactyly, tall stature, and hearing loss syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Camptodactyly, tall stature, and hearing loss syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hearing Loss, Sudden Gene Set

From CTD Gene-Disease Associations

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

Hearing Loss Gene Set

From CTD Gene-Disease Associations

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

Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polyneuropathy, Hearing Loss, Ataxia, Retinitis Pigmentosa, And Cataract from the curated CTD Gene-Disease Associations dataset.

Progressive hearing loss stapes fixation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive hearing loss stapes fixation from the curated CTD Gene-Disease Associations dataset.

Hearing Loss, Conductive Gene Set

From CTD Gene-Disease Associations

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

Hearing Loss, Sensorineural Gene Set

From CTD Gene-Disease Associations

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

Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Mitochondrial Progressive, With Congenital Cataract, Hearing Loss, And Developmental Delay from the curated CTD Gene-Disease Associations dataset.

Hearing Loss, Bilateral Gene Set

From CTD Gene-Disease Associations

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

Hearing Loss Gene Set

From dbGAP Gene-Trait Associations

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

sensorineural hearing loss Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing loss/deafness; osteogenesis imperfecta Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss/deafness; osteogenesis imperfecta in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss; syndrome Gene Set

From GAD Gene-Disease Associations

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

complete hearing loss; deafness; vestibular diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness; vestibular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, central Gene Set

From GAD Gene-Disease Associations

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

autosomal dominant hearing loss Gene Set

From GAD Gene-Disease Associations

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

bone neoplasms; hearing loss; osteosarcoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone neoplasms; hearing loss; osteosarcoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease deafness; diabetes mellitus; hearing loss, sensorineural; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

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

complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sensorineural nonsyndromic Gene Set

From GAD Gene-Disease Associations

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

goiter; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

dominant non-syndromic sensorineural hearing loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dominant non-syndromic sensorineural hearing loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss/deafness; retinal disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hearing loss/deafness; retinal disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

goiter; hearing loss, sensorineural; vertigo Gene Set

From GAD Gene-Disease Associations

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

deafness; hearing loss, sensorineural Gene Set

From GAD Gene-Disease Associations

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

hearing loss, unilateral Gene Set

From GAD Gene-Disease Associations

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

chromosome aberrations; chromosome abnormality; complete hearing loss; deafness Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chromosome aberrations; chromosome abnormality; complete hearing loss; deafness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hearing loss, sudden Gene Set

From GAD Gene-Disease Associations

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

hearing loss/deafness Gene Set

From GAD Gene-Disease Associations

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

nonsyndromic hearing loss Gene Set

From GAD Gene-Disease Associations

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

hearing loss, nonsyndromic sensorineural Gene Set

From GAD Gene-Disease Associations

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

hearing loss, bilateral Gene Set

From GAD Gene-Disease Associations

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

deafness; hearing loss Gene Set

From GAD Gene-Disease Associations

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

goiter; hearing loss, sensorineural; syndrome Gene Set

From GAD Gene-Disease Associations

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

hearing loss, sudden; thrombosis Gene Set

From GAD Gene-Disease Associations

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

hearing loss; noonan syndrome Gene Set

From GAD Gene-Disease Associations

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

presbycusis; hearing loss Gene Set

From GAD Gene-Disease Associations

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

low-frequency hearing loss Gene Set

From HPO Gene-Disease Associations

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

Hearing Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Central Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Unilateral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Functional Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Sensorineural Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Mixed Conductive-Sensorineural Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Bilateral Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Loss, Sudden Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

syndromic hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the syndromic hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

conductive hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the conductive hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

sensorineural hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sensorineural hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

nonsyndromic hearing loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the nonsyndromic hearing loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay phenotype from the curated OMIM Gene-Disease Associations dataset.

?split-hand/foot malformation 1 with sensorineural hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?split-hand/foot malformation 1 with sensorineural hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract Gene Set

From OMIM Gene-Disease Associations

genes associated with the polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.

congenital cataracts, hearing loss, and neurodegeneration Gene Set

From OMIM Gene-Disease Associations

genes associated with the congenital cataracts, hearing loss, and neurodegeneration phenotype from the curated OMIM Gene-Disease Associations dataset.

?peripheral neuropathy, myopathy, hoarseness, and hearing loss Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?peripheral neuropathy, myopathy, hoarseness, and hearing loss phenotype from the curated OMIM Gene-Disease Associations dataset.

alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; coronary disease; diabetes complications; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontal attachment loss; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontitis; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontitis; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontal diseases; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, recurrent; fetal loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; fetal loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; tooth loss Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; chronic periodontitis; dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal loss, late; pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal loss, late; pregnancy loss, recurrent in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; chronic periodontitis; gingival hemorrhage; periodontal attachment loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; chronic periodontitis; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced Gene Set

From CORUM Protein Complexes

proteins in the Death induced signaling complex DISC (FAS, FADD, CASP8, CFLAR), membrane-associated, CD95L induced protein complex from the CORUM Protein Complexes dataset.

Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced Gene Set

From CORUM Protein Complexes

proteins in the Death induced signaling complex II (FADD, CASP8, CFLAR), cytosolic, CD95L induced protein complex from the CORUM Protein Complexes dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pregnancy complications, hematologic; thrombophilia; venous thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced Gene Set

From GAD Gene-Disease Associations

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

fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease fetal diseases; fetal growth retardation; hypertension induced by pregnancy; hypertension, pregnancy-induced; intrauterine growth retardation; pre-eclampsia; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension induced by pregnancy; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

delirium tremens, alcohol withdrawal-induced; seizures, alcohol withdrawal-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease delirium tremens, alcohol withdrawal-induced; seizures, alcohol withdrawal-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acute coronary syndrome; alveolar bone loss; angina pectoris; disease susceptibility; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

decreased susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to weight loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to weight loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{pregnancy loss, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pregnancy loss, recurrent, susceptibility to, 3} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, recurrent, susceptibility to, 3} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pregnancy loss, recurrent, susceptibility to, 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, recurrent, susceptibility to, 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

{pregnancy loss, recurrent, susceptibility to, 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {pregnancy loss, recurrent, susceptibility to, 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 3 from the curated CTD Gene-Disease Associations dataset.

decreased susceptibility to induced joint inflammation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced joint inflammation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to bacterial infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to bacterial infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced pancreatitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced pancreatitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced colitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced colitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced arthritis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced arthritis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced muscular atrophy Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced muscular atrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced retinal damage Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced retinal damage phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to diet-induced obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to diet-induced obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to viral infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to viral infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to induced choroidal neovascularization Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to induced choroidal neovascularization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to parasitic infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to parasitic infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

altered susceptibility to infection induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the altered susceptibility to infection induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

decreased susceptibility to pharmacologically induced seizures Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the decreased susceptibility to pharmacologically induced seizures phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

abnormal susceptibility to induced colitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the abnormal susceptibility to induced colitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{encephalopathy, acute, infection-induced, susceptibility to, 6} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, susceptibility to, 6} phenotype from the curated OMIM Gene-Disease Associations dataset.

{encephalopathy, acute, infection-induced, 3, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, 3, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{angioedema induced by ace inhibitors, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {angioedema induced by ace inhibitors, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{encephalopathy, acute, infection-induced, 4, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {encephalopathy, acute, infection-induced, 4, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{hypersensitivity syndrome, carbamazepine-induced, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {hypersensitivity syndrome, carbamazepine-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

{asthma, aspirin-induced, susceptibility to} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {asthma, aspirin-induced, susceptibility to} phenotype from the curated OMIM Gene-Disease Associations dataset.

increased mortality induced by gamma-irradiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mortality induced by gamma-irradiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased response of heart to induced stress Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased response of heart to induced stress phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased mortality induced by ionizing radiation Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased mortality induced by ionizing radiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sensitivity to xenobiotic induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sensitivity to xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sensitivity to induced cell death Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sensitivity to induced cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased incidence of induced tumors Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased incidence of induced tumors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased sensitivity to induced morbidity/mortality Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased sensitivity to induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased response to stress-induced hyperthermia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased response to stress-induced hyperthermia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased activation-induced b cell apoptosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased activation-induced b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to fractures Gene Set

From HPO Gene-Disease Associations

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

increased susceptibility to systemic lupus erythematosus Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to systemic lupus erythematosus phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to kidney reperfusion injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to kidney reperfusion injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to atherosclerosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to atherosclerosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to type i hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to type i hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to experimental autoimmune uveoretinitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to experimental autoimmune uveoretinitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to autoimmune diabetes Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to autoimmune diabetes phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to autoimmune disorder Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to autoimmune disorder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to dystrophic cardiac calcinosis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to dystrophic cardiac calcinosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to weight gain Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to weight gain phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to experimental autoimmune myasthenia gravis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to experimental autoimmune myasthenia gravis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to dopaminergic neuron neurotoxicity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to dopaminergic neuron neurotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to neuronal excitotoxicity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to neuronal excitotoxicity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to age related obesity Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to age related obesity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to type iii hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to type iii hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to viral infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to viral infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to otitis media Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to otitis media phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to fungal infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to fungal infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to type iv hypersensitivity reaction Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to type iv hypersensitivity reaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to experimental autoimmune encephalomyelitis Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to experimental autoimmune encephalomyelitis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to parasitic infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to parasitic infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to bacterial infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to bacterial infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to autoimmune hemolytic anemia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to autoimmune hemolytic anemia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to graft versus host disease Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to graft versus host disease phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to endotoxin shock Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to endotoxin shock phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to ischemic brain injury Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to ischemic brain injury phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to induction of seizure by inducing agent Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to induction of seizure by inducing agent phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased susceptibility to prion infection Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the increased susceptibility to prion infection phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

increased fatty acid binding increased fat oxidation and insulin resistance Gene Set

From GAD Gene-Disease Associations

genes associated with the disease increased fatty acid binding increased fat oxidation and insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Microtia, hearing impairment, and cleft palate Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microtia, hearing impairment, and cleft palate phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hearing impairment Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hearing impairment phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microtia, Hearing Impairment, And Cleft Palate Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microtia, Hearing Impairment, And Cleft Palate from the curated CTD Gene-Disease Associations dataset.

Hearing Disorders Gene Set

From CTD Gene-Disease Associations

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

Age-Related Hearing Impairment 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Age-Related Hearing Impairment 1 from the curated CTD Gene-Disease Associations dataset.

hearing disorders Gene Set

From GAD Gene-Disease Associations

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

hearing impairment Gene Set

From GAD Gene-Disease Associations

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

nonsyndromic hearing impairment Gene Set

From GAD Gene-Disease Associations

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

hearing Gene Set

From GeneRIF Biological Term Annotations

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

Age-related hearing impairment (interaction) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related hearing impairment (interaction) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Age-related hearing impairment Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Age-related hearing impairment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

Hearing impairment Gene Set

From GWAS Catalog SNP-Phenotype Associations

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

hearing abnormality Gene Set

From GWASdb SNP-Phenotype Associations

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

hearing impairment Gene Set

From GWASdb SNP-Phenotype Associations

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

bilateral sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

progressive hearing impairment Gene Set

From HPO Gene-Disease Associations

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

hearing impairment Gene Set

From HPO Gene-Disease Associations

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

sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

low-frequency sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

hearing abnormality Gene Set

From HPO Gene-Disease Associations

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

conductive hearing impairment Gene Set

From HPO Gene-Disease Associations

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

congenital sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

prelingual sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

postlingual sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

bilateral conductive hearing impairment Gene Set

From HPO Gene-Disease Associations

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

mild hearing impairment Gene Set

From HPO Gene-Disease Associations

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

mild neurosensory hearing impairment Gene Set

From HPO Gene-Disease Associations

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

infantile sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

profound hearing impairment Gene Set

From HPO Gene-Disease Associations

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

progressive sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

childhood onset sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

severe hearing impairment Gene Set

From HPO Gene-Disease Associations

genes associated with the severe hearing impairment 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.

mixed hearing impairment Gene Set

From HPO Gene-Disease Associations

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

severe sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

adult onset sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

progressive conductive hearing impairment Gene Set

From HPO Gene-Disease Associations

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

profound sensorineural hearing impairment Gene Set

From HPO Gene-Disease Associations

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

Hearing Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Hearing Disorders Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

abnormal hearing physiology Gene Set

From MPO Gene-Phenotype Associations

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

sensorineural hearing impairment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the sensorineural hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

conductive hearing impairment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the conductive hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

hearing/vestibular/ear phenotype Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the hearing/vestibular/ear phenotype phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

nonsyndromic hearing impairment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the nonsyndromic hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

syndromic hearing impairment Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the syndromic hearing impairment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

impaired hearing Gene Set

From MPO Gene-Phenotype Associations

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

abnormal hearing electrophysiology Gene Set

From MPO Gene-Phenotype Associations

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

?microtia, hearing impairment, and cleft palate (ar) Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microtia, hearing impairment, and cleft palate (ar) phenotype from the curated OMIM Gene-Disease Associations dataset.

?microtia with or without hearing impairment (ad) Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microtia with or without hearing impairment (ad) phenotype from the curated OMIM Gene-Disease Associations dataset.

{age-related hearing impairment 2} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {age-related hearing impairment 2} phenotype from the curated OMIM Gene-Disease Associations dataset.

{age-related hearing impairment 1} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {age-related hearing impairment 1} phenotype from the curated OMIM Gene-Disease Associations dataset.

coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation Gene Set

From OMIM Gene-Disease Associations

genes associated with the coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation phenotype from the curated OMIM Gene-Disease Associations dataset.

Congenital sensory neuropathy with selective loss of small myelinated fibers Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital sensory neuropathy with selective loss of small myelinated fibers phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Blood Loss, Surgical Gene Set

From CTD Gene-Disease Associations

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

Tooth Loss Gene Set

From CTD Gene-Disease Associations

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

Weight Loss Gene Set

From CTD Gene-Disease Associations

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

Alveolar Bone Loss Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alveolar Bone Loss from the curated CTD Gene-Disease Associations dataset.

Embryo Loss Gene Set

From CTD Gene-Disease Associations

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

hypertension; overweight; weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

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

tooth loss Gene Set

From GAD Gene-Disease Associations

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

inflammation; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

hip bone loss and fracture Gene Set

From GAD Gene-Disease Associations

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

aggressive periodontitis; chronic periodontitis; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; chronic periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, second trimester Gene Set

From GAD Gene-Disease Associations

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

early postmenopausal bone loss at the spine. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early postmenopausal bone loss at the spine. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

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

From GAD Gene-Disease Associations

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

obesity; overweight; weight loss Gene Set

From GAD Gene-Disease Associations

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

mouth, edentulous; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease mouth, edentulous; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiovascular diseases; obesity, morbid; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease cardiovascular diseases; obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; dental plaque; periodontal attachment loss; periodontal diseases; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; dental plaque; periodontal attachment loss; periodontal diseases; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

embryo loss; fetal death Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; fetal death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity; weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

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

h-ras allele loss Gene Set

From GAD Gene-Disease Associations

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

arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri Gene Set

From GAD Gene-Disease Associations

genes associated with the disease arthritis; diabetes, type 1; pregnancy loss, recurrent; juvenile arthritis; pemphigus; il-1ri in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, recurrent; coagulation disorder Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; coagulation disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, recurrent; rhinitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; rhinitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

blood loss, surgical Gene Set

From GAD Gene-Disease Associations

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

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.

fetal loss, late Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss; chronic periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; chronic periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early marginal bone loss around endosseous dental implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous dental implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; weight loss Gene Set

From GAD Gene-Disease Associations

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

body weight; weight loss Gene Set

From GAD Gene-Disease Associations

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

dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dental plaque; gingival hemorrhage; gingival recession; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chronic periodontitis; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease chronic periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

protein loss Gene Set

From GAD Gene-Disease Associations

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

embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; genetic diseases, inborn; pregnancy complications, hematologic; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight loss Gene Set

From GAD Gene-Disease Associations

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

body weight; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

unresolved loss or trauma Gene Set

From GAD Gene-Disease Associations

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

pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

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

obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

polycystic ovary syndrome; pregnancy loss, recurrent Gene Set

From GAD Gene-Disease Associations

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

periodontal attachment loss; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease periodontal attachment loss; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dna damage; embryo loss; hyperhomocysteinemia; recurrence Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dna damage; embryo loss; hyperhomocysteinemia; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; dementia; memory disorders; tooth loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss, recurrent; in vitro fertilization success Gene Set

From GAD Gene-Disease Associations

genes associated with the disease pregnancy loss, recurrent; in vitro fertilization success in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension; obesity; weight loss Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; mandibular diseases; maxillary diseases; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fetal loss, early Gene Set

From GAD Gene-Disease Associations

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

obesity, morbid; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, morbid; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

recurrent early fetal loss Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenocarcinoma; anorexia; stomach neoplasms; syndrome; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; arthritis, rheumatoid; rheumatoid arthritis; sjogren's syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

periodontal attachment loss; periodontitis; tooth mobility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight gain; weight loss Gene Set

From GAD Gene-Disease Associations

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

fetal loss ; thrombophilia Gene Set

From GAD Gene-Disease Associations

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

dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dental occlusion, traumatic; periodontal attachment loss; periodontitis; tooth mobility in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

early marginal bone loss around endosseous implants. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease early marginal bone loss around endosseous implants. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

insulin resistance; overweight; weight loss Gene Set

From GAD Gene-Disease Associations

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

recurrent fetal loss Gene Set

From GAD Gene-Disease Associations

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

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

From GAD Gene-Disease Associations

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

fatty liver; insulin resistance; weight loss Gene Set

From GAD Gene-Disease Associations

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

abortion, habitual; embryo loss; infertility, female Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abortion, habitual; embryo loss; infertility, female in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; periodontitis Gene Set

From GAD Gene-Disease Associations

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

embryo loss; habitual aborter nos; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease embryo loss; habitual aborter nos; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

body weight; fatty liver; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease body weight; fatty liver; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

bone loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bone loss 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.

aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; alveolar bone loss; periodontitis; periodontitis, juvenile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alveolar bone loss; gram-negative bacterial infections; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; gram-negative bacterial infections; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

diabetes, type 2; weight loss; weight gain Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss; dental fistula; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alveolar bone loss; dental fistula; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

pregnancy loss Gene Set

From GAD Gene-Disease Associations

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

lumen loss, late Gene Set

From GAD Gene-Disease Associations

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

aggressive periodontitis; periodontal attachment loss; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; periodontal attachment loss; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, abdominal; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, abdominal; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antisense paternal transcript and loss of imprinting Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antisense paternal transcript and loss of imprinting in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

obesity, morbid; postoperative complications; weight loss Gene Set

From GAD Gene-Disease Associations

genes associated with the disease obesity, morbid; postoperative complications; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

gingival recession; gingivitis; periodontal attachment loss; periodontal diseases; periodontal pocket Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gingival recession; gingivitis; periodontal attachment loss; periodontal diseases; periodontal pocket in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease aggressive periodontitis; chronic periodontitis; dental plaque; gingival hemorrhage; periodontal attachment loss; periodontal pocket; periodontitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

unexplained foetal loss Gene Set

From GAD Gene-Disease Associations

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

alveolar bone loss Gene Set

From GAD Gene-Disease Associations

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

recurrent pregnancy loss Gene Set

From GAD Gene-Disease Associations

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

lossoffunction Gene Set

From GeneRIF Biological Term Annotations

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

lossdriven Gene Set

From GeneRIF Biological Term Annotations

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

lossinduced Gene Set

From GeneRIF Biological Term Annotations

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

lossof Gene Set

From GeneRIF Biological Term Annotations

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

lossofheterozygosity Gene Set

From GeneRIF Biological Term Annotations

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

losses Gene Set

From GeneRIF Biological Term Annotations

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

loss Gene Set

From GeneRIF Biological Term Annotations

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

lossofexpression Gene Set

From GeneRIF Biological Term Annotations

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

lossrelated Gene Set

From GeneRIF Biological Term Annotations

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

lossinactivation Gene Set

From GeneRIF Biological Term Annotations

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

regulation of water loss via skin Gene Set

From GO Biological Process Annotations

genes participating in the regulation of water loss via skin biological process from the curated GO Biological Process Annotations dataset.

Weight loss (gastric bypass surgery) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Weight loss (gastric bypass surgery) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

weight loss Gene Set

From GWASdb SNP-Phenotype Associations

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

loss of ability to walk Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of ability to walk phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of ability to walk in first decade Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of ability to walk in first decade phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of eyelashes Gene Set

From HPO Gene-Disease Associations

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

loss of facial expression Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature loss of teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature loss of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of voice Gene Set

From HPO Gene-Disease Associations

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

loss of subcutaneous adipose tissue in limbs Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of subcutaneous adipose tissue in limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

recurrent loss of toenails and fingernails Gene Set

From HPO Gene-Disease Associations

genes associated with the recurrent loss of toenails and fingernails phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

weight loss Gene Set

From HPO Gene-Disease Associations

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

loss of truncal subcutaneous adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of truncal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

axonal loss Gene Set

From HPO Gene-Disease Associations

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

scalp hair loss Gene Set

From HPO Gene-Disease Associations

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

sudden central visual loss Gene Set

From HPO Gene-Disease Associations

genes associated with the sudden central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive central visual loss Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive central visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

cranial nerve motor loss Gene Set

From HPO Gene-Disease Associations

genes associated with the cranial nerve motor loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of speech Gene Set

From HPO Gene-Disease Associations

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

nonprogressive visual loss Gene Set

From HPO Gene-Disease Associations

genes associated with the nonprogressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neuronal loss in the cerebral cortex Gene Set

From HPO Gene-Disease Associations

genes associated with the neuronal loss in the cerebral cortex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of retinal pigment epithelium Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of retinal pigment epithelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

neuronal loss in basal ganglia Gene Set

From HPO Gene-Disease Associations

genes associated with the neuronal loss in basal ganglia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature loss of permanent teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature loss of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

premature loss of primary teeth Gene Set

From HPO Gene-Disease Associations

genes associated with the premature loss of primary teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

spinal cord posterior columns myelin loss Gene Set

From HPO Gene-Disease Associations

genes associated with the spinal cord posterior columns myelin loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of ability to walk in early childhood Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of ability to walk in early childhood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

visual loss Gene Set

From HPO Gene-Disease Associations

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

loss of consciousness Gene Set

From HPO Gene-Disease Associations

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

neuronal loss in central nervous system Gene Set

From HPO Gene-Disease Associations

genes associated with the neuronal loss in central nervous system phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of facial adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of facial adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

peripheral visual field loss Gene Set

From HPO Gene-Disease Associations

genes associated with the peripheral visual field loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of gluteal subcutaneous adipose tissue Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of gluteal subcutaneous adipose tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

distal sensory loss of all modalities Gene Set

From HPO Gene-Disease Associations

genes associated with the distal sensory loss of all modalities phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

progressive visual loss Gene Set

From HPO Gene-Disease Associations

genes associated with the progressive visual loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

loss of purkinje cells in the cerebellar vermis Gene Set

From HPO Gene-Disease Associations

genes associated with the loss of purkinje cells in the cerebellar vermis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

adipose tissue loss Gene Set

From HPO Gene-Disease Associations

genes associated with the adipose tissue loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Blood Loss, Surgical Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Tooth Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Weight Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Periodontal Attachment Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Periodontal Attachment Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Embryo Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

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

Alveolar Bone Loss Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Alveolar Bone Loss phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

loss of gabaergic neurons Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of gabaergic neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of vibrissae Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of vibrissae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of glutamate neurons Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of glutamate neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of dopaminergic neurons Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of dopaminergic neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of hippocampal neurons Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of hippocampal neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

proximal convoluted tubule brush border loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the proximal convoluted tubule brush border loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

weight loss Gene Set

From MPO Gene-Phenotype Associations

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

partial loss of secondary muscle spindle Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the partial loss of secondary muscle spindle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of basal ganglia neurons Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of basal ganglia neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

premature hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the premature hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of eyelid cilia Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of eyelid cilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

focal dorsal hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

focal hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the focal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

progressive hair loss Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the progressive hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

loss of cortex neurons Gene Set

From MPO Gene-Phenotype Associations

gene mutations causing the loss of cortex neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

{bulimia nervosa, age of onset of weight loss in} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {bulimia nervosa, age of onset of weight loss in} phenotype from the curated OMIM Gene-Disease Associations dataset.

Loss of Function of SMAD4 in Cancer Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of SMAD4 in Cancer pathway from the Reactome Pathways dataset.

Loss of Function of TGFBR2 in Cancer Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of TGFBR2 in Cancer pathway from the Reactome Pathways dataset.

Loss of Nlp from mitotic centrosomes Gene Set

From Reactome Pathways

proteins participating in the Loss of Nlp from mitotic centrosomes pathway from the Reactome Pathways dataset.

Loss of Function of TGFBR1 in Cancer Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of TGFBR1 in Cancer pathway from the Reactome Pathways dataset.

Loss of proteins required for interphase microtubule organization from the centrosome Gene Set

From Reactome Pathways

proteins participating in the Loss of proteins required for interphase microtubule organization from the centrosome pathway from the Reactome Pathways dataset.

Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of FBXW7 in Cancer and NOTCH1 Signaling pathway from the Reactome Pathways dataset.

Loss of Function of SMAD2/3 in Cancer Gene Set

From Reactome Pathways

proteins participating in the Loss of Function of SMAD2/3 in Cancer pathway from the Reactome Pathways dataset.

double stranded rna induced gene expression Gene Set

From Biocarta Pathways

proteins participating in the double stranded rna induced gene expression pathway from the Biocarta Pathways dataset.

lectin induced complement pathway Gene Set

From Biocarta Pathways

proteins participating in the lectin induced complement pathway pathway from the Biocarta Pathways dataset.

cbl mediated ligand-induced downregulation of egf receptors pathway Gene Set

From Biocarta Pathways

proteins participating in the cbl mediated ligand-induced downregulation of egf receptors pathway pathway from the Biocarta Pathways dataset.

fmlp induced chemokine gene expression in hmc-1 cells Gene Set

From Biocarta Pathways

proteins participating in the fmlp induced chemokine gene expression in hmc-1 cells pathway from the Biocarta Pathways dataset.

bioactive peptide induced signaling pathway Gene Set

From Biocarta Pathways

proteins participating in the bioactive peptide induced signaling pathway pathway from the Biocarta Pathways dataset.

tsp-1 induced apoptosis in microvascular endothelial cell Gene Set

From Biocarta Pathways

proteins participating in the tsp-1 induced apoptosis in microvascular endothelial cell pathway from the Biocarta Pathways dataset.

oxidative stress induced gene expression via nrf2 Gene Set

From Biocarta Pathways

proteins participating in the oxidative stress induced gene expression via nrf2 pathway from the Biocarta Pathways dataset.

Cold-induced sweating syndrome 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cold-induced sweating syndrome 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

eNOS-HSP90-AKT complex, VEGF induced Gene Set

From CORUM Protein Complexes

proteins in the eNOS-HSP90-AKT complex, VEGF induced protein complex from the CORUM Protein Complexes dataset.

Bcl-xL-p53-PUMA complex, DNA damage induced Gene Set

From CORUM Protein Complexes

proteins in the Bcl-xL-p53-PUMA complex, DNA damage induced protein complex from the CORUM Protein Complexes dataset.

FAK-beta5 integrin complex, VEGF induced Gene Set

From CORUM Protein Complexes

proteins in the FAK-beta5 integrin complex, VEGF induced protein complex from the CORUM Protein Complexes dataset.

Ksr1-Mek-Braf-Erk complex, EGF induced Gene Set

From CORUM Protein Complexes

proteins in the Ksr1-Mek-Braf-Erk complex, EGF induced protein complex from the CORUM Protein Complexes dataset.

RAF1-RAS complex, EGF induced Gene Set

From CORUM Protein Complexes

proteins in the RAF1-RAS complex, EGF induced protein complex from the CORUM Protein Complexes dataset.

RNA-induced silencing complex, RISC Gene Set

From CORUM Protein Complexes

proteins in the RNA-induced silencing complex, RISC protein complex from the CORUM Protein Complexes dataset.

eNOS-HSP90 complex, VEGF induced Gene Set

From CORUM Protein Complexes

proteins in the eNOS-HSP90 complex, VEGF induced protein complex from the CORUM Protein Complexes dataset.

CRMP-MICAL-PlexinA1 complex, induced by SEMA3A Gene Set

From CORUM Protein Complexes

proteins in the CRMP-MICAL-PlexinA1 complex, induced by SEMA3A protein complex from the CORUM Protein Complexes dataset.

Wave1-Bcl-xl-Pancortin-2 complex, focal ischemic stroke induced Gene Set

From CORUM Protein Complexes

proteins in the Wave1-Bcl-xl-Pancortin-2 complex, focal ischemic stroke induced protein complex from the CORUM Protein Complexes dataset.

Ask1-Traf6 complex, LPS induced Gene Set

From CORUM Protein Complexes

proteins in the Ask1-Traf6 complex, LPS induced protein complex from the CORUM Protein Complexes dataset.

Ksr1-Mek-Braf complex, EGF induced Gene Set

From CORUM Protein Complexes

proteins in the Ksr1-Mek-Braf complex, EGF induced protein complex from the CORUM Protein Complexes dataset.

p53-Bcl-xL complex, DNA-damage induced Gene Set

From CORUM Protein Complexes

proteins in the p53-Bcl-xL complex, DNA-damage induced protein complex from the CORUM Protein Complexes dataset.

PUMA-Bcl-xL complex, DNA-damage induced Gene Set

From CORUM Protein Complexes

proteins in the PUMA-Bcl-xL complex, DNA-damage induced protein complex from the CORUM Protein Complexes dataset.

Neoplasms, Radiation-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neoplasms, Radiation-Induced from the curated CTD Gene-Disease Associations dataset.

Cold-Induced Sweating Syndrome 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cold-Induced Sweating Syndrome 1 from the curated CTD Gene-Disease Associations dataset.

Dyskinesia, Drug-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dyskinesia, Drug-Induced from the curated CTD Gene-Disease Associations dataset.

Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epilepsy, rolandic with paroxysmal exercise-induced dystonia and writer's cramp from the curated CTD Gene-Disease Associations dataset.

Alcohol-Induced Disorders, Nervous System Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alcohol-Induced Disorders, Nervous System from the curated CTD Gene-Disease Associations dataset.

Drug-Induced Liver Injury, Chronic Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug-Induced Liver Injury, Chronic from the curated CTD Gene-Disease Associations dataset.

Deafness, Aminoglycoside-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, Aminoglycoside-Induced from the curated CTD Gene-Disease Associations dataset.

Radiation induced meningioma Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Radiation induced meningioma from the curated CTD Gene-Disease Associations dataset.

Drug-Induced Liver Injury Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Drug-Induced Liver Injury from the curated CTD Gene-Disease Associations dataset.

Asthma, Aspirin-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Asthma, Aspirin-Induced from the curated CTD Gene-Disease Associations dataset.

Psychoses, Substance-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Psychoses, Substance-Induced from the curated CTD Gene-Disease Associations dataset.

Hypertension, Pregnancy-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Pregnancy-Induced from the curated CTD Gene-Disease Associations dataset.

Hypoglycemia, leucine-induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypoglycemia, leucine-induced from the curated CTD Gene-Disease Associations dataset.

Asthma, Exercise-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Asthma, Exercise-Induced from the curated CTD Gene-Disease Associations dataset.

Abnormalities, Drug-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Abnormalities, Drug-Induced from the curated CTD Gene-Disease Associations dataset.

Akathisia, Drug-Induced Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Akathisia, Drug-Induced from the curated CTD Gene-Disease Associations dataset.

Drug-Induced Liver Injury Gene Set

From dbGAP Gene-Trait Associations

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

drug-induced hepatitis Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease drug-induced hepatitis in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

drug-induced hepatitis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

substance-induced psychosis Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

alcohol-induced mental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease alcohol-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

drug-induced mental disorder Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease drug-induced mental disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

steroid-induced glaucoma Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

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

tpa-induced apoptosis Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; hematologic diseases; hepatitis, toxic; large-cell lymphomas; lymphoma, large b-cell, diffuse; mucositis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hematologic diseases; hepatitis, toxic; large-cell lymphomas; lymphoma, large b-cell, diffuse; mucositis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

adenosine diphosphate-induced platelet aggregation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease adenosine diphosphate-induced platelet aggregation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; precursor cell lymphoblastic leukemia-lymphoma Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; precursor cell lymphoblastic leukemia-lymphoma in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; cocarcinogenesis; neoplasms, radiation-induced; skin basal cell carcinoma; skin neoplasms; squamous cell carcinoma; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced Gene Set

From GAD Gene-Disease Associations

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

preeclampsia; hypertension, pregnancy induced Gene Set

From GAD Gene-Disease Associations

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

risperidone-induced extrapyramidal symptoms Gene Set

From GAD Gene-Disease Associations

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

erythropoietin induced hypertension Gene Set

From GAD Gene-Disease Associations

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

eclampsia; hypertension, pregnancy-induced; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease eclampsia; hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury, chronic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury, chronic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced; movement disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyskinesia, drug-induced; movement disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, papillary; lymphatic metastasis; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, papillary; lymphatic metastasis; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, radiation-induced; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, radiation-induced; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma, aspirin-induced; urticaria, aspirin-intolerant Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma, aspirin-induced; urticaria, aspirin-intolerant in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

psychoses, substance-induced; substance-related disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease psychoses, substance-induced; substance-related disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

phenytoin-induced congenital malformations Gene Set

From GAD Gene-Disease Associations

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

lupus erythematosus; nephrotic syndrome; agranulocytosis, drug induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus; nephrotic syndrome; agranulocytosis, drug induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chemotherapy-induced pulmonary fibrosis Gene Set

From GAD Gene-Disease Associations

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

akathisia, drug-induced; Gene Set

From GAD Gene-Disease Associations

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

antipsychotic-induced adverse reactions Gene Set

From GAD Gene-Disease Associations

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

pregnancy-induced chylomicronemia Gene Set

From GAD Gene-Disease Associations

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

bipolar disorder; mania, antidepressant-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease bipolar disorder; mania, antidepressant-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury (flucloxacillin) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury (flucloxacillin) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

basal ganglia diseases; dyskinesia, drug-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease basal ganglia diseases; dyskinesia, drug-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; pre-eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma (toluene diisocyanate-induced) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma (toluene diisocyanate-induced) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, papillary; dna damage; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, papillary; dna damage; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

agitation; dyskinesia, drug-induced; psychomotor agitation Gene Set

From GAD Gene-Disease Associations

genes associated with the disease agitation; dyskinesia, drug-induced; psychomotor agitation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

weight gain (antipsychotic-drug induced) Gene Set

From GAD Gene-Disease Associations

genes associated with the disease weight gain (antipsychotic-drug induced) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; graft vs host disease; inflammation; leukemia; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; graft vs host disease; inflammation; leukemia; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

radiation-induced ocular telangiectasia Gene Set

From GAD Gene-Disease Associations

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

amphetamine-related disorders; psychoses, substance-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease amphetamine-related disorders; psychoses, substance-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

heparin-induced thrombocytopenia Gene Set

From GAD Gene-Disease Associations

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

caffeine-induced anxiety. Gene Set

From GAD Gene-Disease Associations

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

hdac inhibitor-induced growth arrest. Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hdac inhibitor-induced growth arrest. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced long-qt syndrome Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced long-qt syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-induced disorders; esophageal neoplasms; liver cirrhosis, alcoholic; oesophageal neoplasm; pancreatitis, alcoholic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; pre-eclampsia; thrombophilia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hypertension, pregnancy-induced; pre-eclampsia; thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antipsychotic agent-induced weight gain Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antipsychotic agent-induced weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; latent tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; latent tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, radiation-induced; occupational diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, radiation-induced; occupational diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

cardiotoxicity, anthracycline-induced Gene Set

From GAD Gene-Disease Associations

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

marijuana abuse; psychoses, substance-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease marijuana abuse; psychoses, substance-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

antibiotic-induced cutaneous allergic reactions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease antibiotic-induced cutaneous allergic reactions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

abnormalities, drug-induced; epilepsy; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, drug-induced; epilepsy; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesias, levodopa-induced Gene Set

From GAD Gene-Disease Associations

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

methamphetamine induced psychosis Gene Set

From GAD Gene-Disease Associations

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

asthma, exercise-induced Gene Set

From GAD Gene-Disease Associations

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

gingival overgrowth, drug induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease gingival overgrowth, drug induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

nevirapine-induced rash-hiv Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; gastrointestinal diseases; psoriasis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; gastrointestinal diseases; psoriasis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

anticholinergic challenge-induced memory impairment Gene Set

From GAD Gene-Disease Associations

genes associated with the disease anticholinergic challenge-induced memory impairment in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; hepatitis, toxic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hepatitis, toxic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury Gene Set

From GAD Gene-Disease Associations

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

preeclampsia; hypertension, pregnancy induced; eclampsia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease preeclampsia; hypertension, pregnancy induced; eclampsia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

mania, antidepressant-induced Gene Set

From GAD Gene-Disease Associations

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

arsenic-induced hyperkeratosis Gene Set

From GAD Gene-Disease Associations

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

morphine-induced adverse drug reactions Gene Set

From GAD Gene-Disease Associations

genes associated with the disease morphine-induced adverse drug reactions in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

helicobacter pylori infection; gastritis, helicobacter pylori-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease helicobacter pylori infection; gastritis, helicobacter pylori-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

inflammatory response, trauma induced Gene Set

From GAD Gene-Disease Associations

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

akathisia, drug-induced Gene Set

From GAD Gene-Disease Associations

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

hodgkin disease; neoplasms, radiation-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease hodgkin disease; neoplasms, radiation-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

asthma, exercise-induced; bronchial hyperreactivity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease asthma, exercise-induced; bronchial hyperreactivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

exercise-induced changes in insulin Gene Set

From GAD Gene-Disease Associations

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

agranulocytosis, drug induced Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; hepatitis, toxic; tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hepatitis, toxic; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; liver diseases; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; liver diseases; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced; parkinsonian disorders Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyskinesia, drug-induced; parkinsonian disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, papillary; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, papillary; neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-induced disorders, nervous system; alcoholism Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-induced disorders, nervous system; alcoholism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-induced disorders; esophageal neoplasms; laryngeal neoplasms; oropharyngeal neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; epilepsy; hepatitis, toxic Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; epilepsy; hepatitis, toxic in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; tuberculosis Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; tuberculosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

fluvastatin induced cholesterol changes Gene Set

From GAD Gene-Disease Associations

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

lupus erythematosus; agranulocytosis, drug induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lupus erythematosus; agranulocytosis, drug induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcohol-induced disorders; prenatal exposure delayed effects Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcohol-induced disorders; prenatal exposure delayed effects in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

delirium tremens, alcohol withdrawal-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease delirium tremens, alcohol withdrawal-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; hematologic diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hematologic diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

aspirin-induced asthma Gene Set

From GAD Gene-Disease Associations

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

pollen-induced allergic rhinitis Gene Set

From GAD Gene-Disease Associations

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

akathisia, drug-induced; dystonia Gene Set

From GAD Gene-Disease Associations

genes associated with the disease akathisia, drug-induced; dystonia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease neoplasms, radiation-induced; thyroid neoplasm; thyroid neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

alcoholism; delirium tremens, alcohol-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alcoholism; delirium tremens, alcohol-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy-induced; proteinuria Gene Set

From GAD Gene-Disease Associations

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

radiation-induced damage to normal tissues Gene Set

From GAD Gene-Disease Associations

genes associated with the disease radiation-induced damage to normal tissues in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hcv-induced liver fibrosis Gene Set

From GAD Gene-Disease Associations

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

delirium tremens, alcohol-induced; alcohol withdrawal Gene Set

From GAD Gene-Disease Associations

genes associated with the disease delirium tremens, alcohol-induced; alcohol withdrawal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn Gene Set

From GAD Gene-Disease Associations

genes associated with the disease carcinoma, basal cell; carcinoma, squamous cell; neoplasms, radiation-induced; skin neoplasms; sunburn in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

clozapine-induced agranulocytosis Gene Set

From GAD Gene-Disease Associations

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

weight gain, antipsychotic drug-induced Gene Set

From GAD Gene-Disease Associations

genes associated with the disease weight gain, antipsychotic drug-induced in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced; Gene Set

From GAD Gene-Disease Associations

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

abnormalities, drug-induced; cleft lip; cleft palate Gene Set

From GAD Gene-Disease Associations

genes associated with the disease abnormalities, drug-induced; cleft lip; cleft palate in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

chemotherapy-induced leukemia Gene Set

From GAD Gene-Disease Associations

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

drug-induced liver injury; hepatitis, toxic; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; hepatitis, toxic; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

hypertension, pregnancy induced Gene Set

From GAD Gene-Disease Associations

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

alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases Gene Set

From GAD Gene-Disease Associations

genes associated with the disease alzheimer disease; alzheimer's disease; drug-induced liver injury; liver diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; tuberculosis, pulmonary Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; tuberculosis, pulmonary in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms Gene Set

From GAD Gene-Disease Associations

genes associated with the disease brill-symmers disease; lymphoma, follicular; lymphoma, large b-cell, diffuse; lymphoma, large-cell, diffuse; neoplasms, radiation-induced; skin neoplasms in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

drug-induced liver injury; liver failure, acute Gene Set

From GAD Gene-Disease Associations

genes associated with the disease drug-induced liver injury; liver failure, acute in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

dyskinesia, drug-induced; obesity Gene Set

From GAD Gene-Disease Associations

genes associated with the disease dyskinesia, drug-induced; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

the extent of exercise-induced left ventricular growth in endurance athletes Gene Set

From GAD Gene-Disease Associations

genes associated with the disease the extent of exercise-induced left ventricular growth in endurance athletes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

psychoses, substance-induced Gene Set

From GAD Gene-Disease Associations

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

induced Gene Set

From GeneRIF Biological Term Annotations

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

E2F3_KD_GDS4094_448_mouse_Mammary tumors (Myc-induced) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the E2F3_KD_GDS4094_448_mouse_Mammary tumors (Myc-induced) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

TGM2_KD_GSE23702_716_human_NB4 cells, 72h ATRA-induced differentiation Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the TGM2_KD_GSE23702_716_human_NB4 cells, 72h ATRA-induced differentiation gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

E2F2_KD_GDS4094_447_mouse_Mammary tumors (Myc-induced) Gene Set

From GEO Signatures of Differentially Expressed Genes for Gene Perturbations

genes differentially expressed following the E2F2_KD_GDS4094_447_mouse_Mammary tumors (Myc-induced) gene perturbation from the GEO Signatures of Differentially Expressed Genes for Gene Perturbations dataset.

negative regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

histamine-induced gastric acid secretion Gene Set

From GO Biological Process Annotations

genes participating in the histamine-induced gastric acid secretion biological process from the curated GO Biological Process Annotations dataset.

regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

activation-induced cell death of t cells Gene Set

From GO Biological Process Annotations

genes participating in the activation-induced cell death of t cells biological process from the curated GO Biological Process Annotations dataset.

gastrin-induced gastric acid secretion Gene Set

From GO Biological Process Annotations

genes participating in the gastrin-induced gastric acid secretion biological process from the curated GO Biological Process Annotations dataset.

regulation of hypoxia-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of hypoxia-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

mitochondrion degradation by induced vacuole formation Gene Set

From GO Biological Process Annotations

genes participating in the mitochondrion degradation by induced vacuole formation biological process from the curated GO Biological Process Annotations dataset.

negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of viral-induced cytoplasmic pattern recognition receptor signaling pathway biological process from the curated GO Biological Process Annotations dataset.

dna damage induced protein phosphorylation Gene Set

From GO Biological Process Annotations

genes participating in the dna damage induced protein phosphorylation biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

regulation of oxidative stress-induced intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the regulation of oxidative stress-induced intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-induced neuron intrinsic apoptotic signaling pathway Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of hydrogen peroxide-induced neuron intrinsic apoptotic signaling pathway biological process from the curated GO Biological Process Annotations dataset.

positive regulation of oxidative stress-induced cell death Gene Set

From GO Biological Process Annotations

genes participating in the positive regulation of oxidative stress-induced cell death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of oxidative stress-induced neuron death Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of oxidative stress-induced neuron death biological process from the curated GO Biological Process Annotations dataset.

negative regulation of hydrogen peroxide-induced cell death Gene Set