| Name |
|---|
TAM GeneMyeloproliferative syndrome, transient (transient abnormal |
ASPM Geneasp (abnormal spindle) homolog, microcephaly associated (Drosophila) This gene is the human ortholog of the Drosophila melanogaster 'abnormal spindle' gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts. Studies in mouse also suggest a role of this gene in mitotic spindle regulation, with a preferential role in regulating neurogenesis. Mutations in this gene are associated with microcephaly primary type 5. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011] |
HILPDA Genehypoxia inducible lipid droplet-associated Enables signaling receptor binding activity. Involved in several processes, including autocrine signaling; cellular response to hypoxia; and positive regulation of lipid storage. Located in several cellular components, including cell surface; lipid droplet; and secretory granule. Implicated in colorectal cancer and hepatocellular carcinoma. Biomarker of colorectal cancer and hepatocellular carcinoma. [provided by Alliance of Genome Resources, Mar 2025] |
LOC400927 GeneTPTE and PTEN homologous inositol lipid phosphatase pseudogene |
LDAH Genelipid droplet associated hydrolase Predicted to enable sterol ester esterase activity. Involved in cholesterol homeostasis and intracellular triglyceride homeostasis. Acts upstream of with a positive effect on lipid droplet fusion. Located in endoplasmic reticulum and lipid droplet. [provided by Alliance of Genome Resources, Mar 2025] |
STARD10 GeneStAR-related lipid transfer (START) domain containing 10 Predicted to enable lipid binding activity. Predicted to be involved in lipid transport. Predicted to act upstream of or within bile acid secretion and positive regulation of peroxisome proliferator activated receptor signaling pathway. Located in cytosol. [provided by Alliance of Genome Resources, Mar 2025] |
STARD13 GeneStAR-related lipid transfer (START) domain containing 13 This gene encodes a protein which contains an N-terminal sterile alpha motif (SAM) for protein-protein interactions, followed by an ATP/GTP-binding motif, a GTPase-activating protein (GAP) domain, and a C-terminal STAR-related lipid transfer (START) domain. It may be involved in regulation of cytoskeletal reorganization, cell proliferation, and cell motility, and acts as a tumor suppressor in hepatoma cells. The gene is located in a region of chromosome 13 that is associated with loss of heterozygosity in hepatocellular carcinomas. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Aug 2011] |
STARD9 GeneStAR-related lipid transfer (START) domain containing 9 Enables microtubule binding activity and microtubule motor activity. Involved in spindle assembly. Located in centriole; cytoplasm; and nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
STARD4 GeneStAR-related lipid transfer (START) domain containing 4 Cholesterol homeostasis is regulated, at least in part, by sterol regulatory element (SRE)-binding proteins (e.g., SREBP1; MIM 184756) and by liver X receptors (e.g., LXRA; MIM 602423). Upon sterol depletion, LXRs are inactive and SREBPs are cleaved, after which they bind promoter SREs and activate genes involved in cholesterol biosynthesis and uptake. Sterol transport is mediated by vesicles or by soluble protein carriers, such as steroidogenic acute regulatory protein (STAR; MIM 600617). STAR is homologous to a family of proteins containing a 200- to 210-amino acid STAR-related lipid transfer (START) domain, including STARD4 (Soccio et al., 2002 [PubMed 12011452]).[supplied by OMIM, Mar 2008] |
STARD5 GeneStAR-related lipid transfer (START) domain containing 5 Proteins containing a steroidogenic acute regulatory-related lipid transfer (START) domain are often involved in the trafficking of lipids and cholesterol between diverse intracellular membranes. This gene is a member of the StarD subfamily that encodes START-related lipid transfer proteins. The protein encoded by this gene is a cholesterol transporter and is also able to bind and transport other sterol-derived molecules related to the cholesterol/bile acid biosynthetic pathways such as 25-hydroxycholesterol. Its expression is upregulated during endoplasmic reticulum (ER) stress. The protein is thought to act as a cytosolic sterol transporter that moves cholesterol between intracellular membranes such as from the cytoplasm to the ER and from the ER to the Golgi apparatus. Alternative splicing of this gene produces multiple transcript variants. [provided by RefSeq, Jan 2016] |
ERLIN1 GeneER lipid raft associated 1 The protein encoded by this gene is part of a protein complex that mediates degradation of inositol 1,4,5-trisphosphate receptors in the endoplasmic reticulum. The encoded protein also binds cholesterol and regulates the SREBP signaling pathway, which promotes cellular cholesterol homeostasis. Defects in this gene have been associated with spastic paraplegia 62. [provided by RefSeq, Dec 2016] |
ERLIN2 GeneER lipid raft associated 2 This gene encodes a member of the SPFH domain-containing family of lipid raft-associated proteins. The encoded protein is localized to lipid rafts of the endoplasmic reticulum and plays a critical role in inositol 1,4,5-trisphosphate (IP3) signaling by mediating ER-associated degradation of activated IP3 receptors. Mutations in this gene are a cause of spastic paraplegia-18 (SPG18). Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2012] |
LPPR3 Genelipid phosphate phosphatase-related protein type 3 The proteins in the lipid phosphate phosphatase (LPP) family, including PRG2, are integral membrane proteins that modulate bioactive lipid phosphates including phosphatidate, lysophosphatidate, and sphingosine-1-phosphate in the context of cell migration, neurite retraction, and mitogenesis (Brauer et al., 2003 [PubMed 12730698]).[supplied by OMIM, Mar 2008] |
RFTN1 Generaftlin, lipid raft linker 1 Enables double-stranded RNA binding activity. Involved in B cell receptor signaling pathway; membrane raft assembly; and positive regulation of growth rate. Acts upstream of or within dsRNA transport; response to exogenous dsRNA; and toll-like receptor 3 signaling pathway. Located in endosome; membrane raft; and plasma membrane. Part of protein-containing complex. Biomarker of glaucoma. [provided by Alliance of Genome Resources, Mar 2025] |
RFTN1P1 Generaftlin, lipid raft linker 1 pseudogene 1 |
LPPR5 Genelipid phosphate phosphatase-related protein type 5 The protein encoded by this gene is a type 2 member of the phosphatidic acid phosphatase (PAP) family. All type 2 members of this protein family contain 6 transmembrane regions, and a consensus N-glycosylation site. PAPs convert phosphatidic acid to diacylglycerol, and function in de novo synthesis of glycerolipids as well as in receptor-activated signal transduction mediated by phospholipase D. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
LPPR4 Genelipid phosphate phosphatase-related protein type 4 The protein encoded by this gene belongs to the lipid phosphate phosphatase (LPP) family. LPPs catalyze the dephosphorylation of a number of bioactive lipid mediators that regulate a variety of cell functions. This protein is specifically expressed in neurons. It is located in the membranes of outgrowing axons and has been shown to be important for axonal outgrowth during development and regenerative sprouting. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009] |
LPPR2 Genelipid phosphate phosphatase-related protein type 2 Predicted to enable phosphatidate phosphatase activity. Predicted to be involved in phospholipid dephosphorylation; phospholipid metabolic process; and signal transduction. Predicted to be located in membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
LPPR1 Genelipid phosphate phosphatase-related protein type 1 This gene encodes a member of the plasticity-related gene (PRG) family. Members of the PRG family mediate lipid phosphate phosphatase activity in neurons and are known to be involved in neuronal plasticity. The protein encoded by this gene does not perform its function through enzymatic phospholipid degradation. This gene is strongly expressed in brain. It shows dynamic expression regulation during brain development and neuronal excitation. Alternatively spliced transcript variants encoding the same protein have been observed. [provided by RefSeq, Jul 2008] |
STARD8 GeneStAR-related lipid transfer (START) domain containing 8 This gene encodes a member of a subfamily of Rho GTPase activating proteins that contain a steroidogenic acute regulatory protein related lipid transfer domain. The encoded protein localizes to focal adhesions and may be involved in regulating cell morphology. This protein may also function as a tumor suppressor. [provided by RefSeq, Mar 2010] |
STARD3 GeneStAR-related lipid transfer (START) domain containing 3 This gene encodes a member of a subfamily of lipid trafficking proteins that are characterized by a C-terminal steroidogenic acute regulatory domain and an N-terminal metastatic lymph node 64 domain. The encoded protein localizes to the membranes of late endosomes and may be involved in exporting cholesterol. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009] |
STARD6 GeneStAR-related lipid transfer (START) domain containing 6 Cholesterol homeostasis is regulated, at least in part, by sterol regulatory element (SRE)-binding proteins (e.g., SREBP1; MIM 184756) and by liver X receptors (e.g., LXRA; MIM 602423). Upon sterol depletion, LXRs are inactive and SREBPs are cleaved, after which they bind promoter SREs and activate genes involved in cholesterol biosynthesis and uptake. Sterol transport is mediated by vesicles or by soluble protein carriers, such as steroidogenic acute regulatory protein (STAR; MIM 600617). STAR is homologous to a family of proteins containing a 200- to 210-amino acid STAR-related lipid transfer (START) domain, including STARD6 (Soccio et al., 2002 [PubMed 12011452]).[supplied by OMIM, Mar 2008] |
STARD7 GeneStAR-related lipid transfer (START) domain containing 7 Predicted to enable lipid transfer activity. Predicted to be involved in ubiquinone biosynthetic process. Predicted to act upstream of or within several processes, including establishment of skin barrier; mucociliary clearance; and myeloid dendritic cell activation. Located in mitochondrion. Implicated in familial adult myoclonic epilepsy 2. [provided by Alliance of Genome Resources, Mar 2025] |
LOC100131127 Genedegenerative spermatocyte homolog 1, lipid desaturase (Drosophila) pseudogene |
ILRUN Geneinflammation and lipid regulator with UBA-like and NBR1-like domains This gene encodes a protein with N-terminal ubiquitin-associated (UBA)-like and central neighbor of BRCA1 gene 1 (NBR1)-like domains. The protein acts an inhibitor of antiviral and proinflammatory cytokine transcription and as a regulator of the renin-angiotensin-aldosterone system (RAAS). [provided by RefSeq, Jul 2021] |
BLTP2 Genebridge-like lipid transfer protein family member 2 This gene was initially characterized in human as having high expression levels in breast carcinomas and breast cancer cell lines. This gene also has increased expression in prostrate cancer cells relative to normal prostrate tissues. Expression of this gene is negatively regulated by direct binding of the microRNA miR-195 to its 3' UTR. miR-195 has been shown to modulate the invasiveness of prostrate cancer cells and xenograft metastases by downgrading expression of this gene. In mouse, the protein encoded by this gene was identified as an antigen on acute monocytic leukemia cells. In human, alternative splicing results in multiple transcript variants encoding distinct isoforms; some of these isoforms are predicted to contain an RNA pol II promoter FMP27 protein domain and a Golgi-body-localization APT1 domain. [provided by RefSeq, Apr 2017] |
BLTP1 Genebridge-like lipid transfer protein family member 1 This gene is located on the long arm of chromosome 4 in a region that is associated with susceptibility to celiac disease. The encoded protein is similar to a Chinese hamster protein that is associated with spermatocyte and adipocyte differentiation. The C-terminus of the protein is also similar to a Caenorhabditis elegans protein that plays a role in lipid storage. In mammals, this protein is thought to function in the regulation of epithelial growth and differentiation, and in tumor development. [provided by RefSeq, Oct 2009] |
LDAF1 Genelipid droplet assembly factor 1 Involved in lipid droplet formation. Located in endoplasmic reticulum membrane and lipid droplet. [provided by Alliance of Genome Resources, Mar 2025] |
BLTP3B Genebridge-like lipid transfer protein family member 3B Enables GARP complex binding activity; lipid transfer activity; and protein homodimerization activity. Involved in early endosome to Golgi transport and intermembrane lipid transfer. Located in cytosol and early endosome. [provided by Alliance of Genome Resources, Mar 2025] |
HYCC2 Genehyccin PI4KA lipid kinase complex subunit 2 Predicted to be involved in phosphatidylinositol phosphate biosynthetic process and protein localization to plasma membrane. Predicted to be located in cytosol and membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Mar 2025] |
BLTP3A Genebridge-like lipid transfer protein family member 3A Enables histone deacetylase binding activity and identical protein binding activity. Located in late endosome. [provided by Alliance of Genome Resources, Mar 2025] |
HYCC1 Genehyccin PI4KA lipid kinase complex subunit 1 The protein encoded by this gene may play a part in the beta-catenin/Lef signaling pathway. Expression of this gene is down-regulated by beta-catenin. Defects in this gene are a cause of hypomyelination with congenital cataract (HCC). [provided by RefSeq, Oct 2008] |
LTAP1 Genelipid transport auxiliary protein 1 |
APOLTP Geneapolipoprotein lipid transfer particle homolog |
Abnormal Lipid Deposits Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Lipid Deposits in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
lipid transport involved in lipid storage Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid transport involved in lipid storage biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid transport involved in lipid storage Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid transport involved in lipid storage biological process from the curated GO Biological Process Annotations 2025 dataset. |
visceral fat deposits and the metabolic syndrome Gene SetFrom Biocarta Pathways proteins participating in the visceral fat deposits and the metabolic syndrome pathway from the Biocarta Pathways dataset. |
Glomerulopathy with fibronectin deposits 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Glomerulopathy with fibronectin deposits 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Glomerulopathy with fibronectin deposits Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Glomerulopathy with fibronectin deposits from the curated CTD Gene-Disease Associations dataset. |
deposits Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term deposits in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
conjunctival whitish salt-like deposits Gene SetFrom HPO Gene-Disease Associations genes associated with the conjunctival whitish salt-like deposits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
deposits immunoreactive to beta-amyloid protein Gene SetFrom HPO Gene-Disease Associations genes associated with the deposits immunoreactive to beta-amyloid protein phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
granular osmiophilic deposits (grod) in cells Gene SetFrom HPO Gene-Disease Associations genes associated with the granular osmiophilic deposits (grod) in cells phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
pigmentary retinal deposits Gene SetFrom HPO Gene-Disease Associations genes associated with the pigmentary retinal deposits phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
retinal deposits Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the retinal deposits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
corneal deposits Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the corneal deposits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
tau protein deposits Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the tau protein deposits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
amyloid beta deposits Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the amyloid beta deposits phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
glomerulopathy with fibronectin deposits 1 Gene SetFrom OMIM Gene-Disease Associations genes associated with the glomerulopathy with fibronectin deposits 1 phenotype from the curated OMIM Gene-Disease Associations dataset. |
glomerulopathy with fibronectin deposits 2 Gene SetFrom OMIM Gene-Disease Associations genes associated with the glomerulopathy with fibronectin deposits 2 phenotype from the curated OMIM Gene-Disease Associations dataset. |
Glomerulopathy With Fibronectin Deposits Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glomerulopathy With Fibronectin Deposits in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Glomerulopathy With Fibronectin Deposits 2 (Disorder) Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Glomerulopathy With Fibronectin Deposits 2 (Disorder) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Deposits Immunoreactive To Beta-Amyloid Protein Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Deposits Immunoreactive To Beta-Amyloid Protein in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sub-Rpe Deposits Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sub-Rpe Deposits in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Glomerular Subendothelial Electron-Dense Deposits Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Glomerular Subendothelial Electron-Dense Deposits in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Corneal Crystalline Deposits Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Corneal Crystalline Deposits in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Granular Osmiophilic Deposits (Grod) In Cells Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Granular Osmiophilic Deposits (Grod) In Cells in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Subretinal Deposits Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Subretinal Deposits in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Conjunctival Whitish Salt-Like Deposits Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Conjunctival Whitish Salt-Like Deposits in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
retina deposits Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the retina deposits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal glomerular immunoglobulin deposits Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerular immunoglobulin deposits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
renal glomerular protein deposits Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the renal glomerular protein deposits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
amyloid beta deposits Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the amyloid beta deposits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal deposits Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the corneal deposits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
tau protein deposits Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the tau protein deposits phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
corneal deposits Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the corneal deposits phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal lipid metabolism Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipid metabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sebaceous lipid secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sebaceous lipid secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown fat lipid droplet number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown fat lipid droplet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal stratum corneum lipid matrix formation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal stratum corneum lipid matrix formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestinal lipid absorption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestinal lipid absorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal white fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipid homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipid homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lipid level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lipid level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipid oxidation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lipid oxidation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lipid homeostasis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lipid homeostasis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal sebaceous lipid secretion Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal sebaceous lipid secretion phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal intestinal lipid absorption Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal intestinal lipid absorption phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal stratum corneum lipid matrix formation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal stratum corneum lipid matrix formation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal circulating lipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal circulating lipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lipid oxidation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lipid oxidation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal lipid metabolism Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal lipid metabolism phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal ether lipid level Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal ether lipid level phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Abnormal circulating lipid concentration Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Abnormal circulating lipid concentration phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
srebp control of lipid synthesis Gene SetFrom Biocarta Pathways proteins participating in the srebp control of lipid synthesis pathway from the Biocarta Pathways dataset. |
Neutral lipid storage disease with myopathy Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Neutral lipid storage disease with myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lipid proteinosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lipid proteinosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
lipid particle Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lipid particle cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
protein-lipid complex Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the protein-lipid complex cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
lipid tube Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lipid tube cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
organelle-enclosing lipid monolayer Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the organelle-enclosing lipid monolayer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
protein-lipid complex Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the protein-lipid complex cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
monolayer-surrounded lipid storage body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the monolayer-surrounded lipid storage body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
lipid particle Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lipid particle cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
lipid tube Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lipid tube cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
lipid mobilizing substance Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical lipid mobilizing substance from the curated CTD Gene-Chemical Interactions dataset. |
Lipid Peroxides Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Lipid Peroxides from the curated CTD Gene-Chemical Interactions dataset. |
lipid-linked oligosaccharides Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical lipid-linked oligosaccharides from the curated CTD Gene-Chemical Interactions dataset. |
monophosphoryl lipid A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical monophosphoryl lipid A from the curated CTD Gene-Chemical Interactions dataset. |
Lipid A Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Lipid A from the curated CTD Gene-Chemical Interactions dataset. |
Lipid Metabolism, Inborn Errors Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipid Metabolism, Inborn Errors from the curated CTD Gene-Disease Associations dataset. |
Neutral Lipid Storage Disease with Myopathy Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutral Lipid Storage Disease with Myopathy from the curated CTD Gene-Disease Associations dataset. |
Lipid Metabolism Disorders Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lipid Metabolism Disorders from the curated CTD Gene-Disease Associations dataset. |
Lipid Metabolism Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Lipid Metabolism in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
lipid storage disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease lipid storage disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
neutral lipid storage disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease neutral lipid storage disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
lipid metabolism disorder Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease lipid metabolism disorder from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
lipid storage disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease lipid storage disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
lipid metabolism disorder Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease lipid metabolism disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
lipid metabolism disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lipid metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lipid pneumonia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lipid pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lipid-rich carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lipid-rich carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lipid storage disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lipid storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
neutral lipid storage disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease neutral lipid storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lipid metabolism disorders; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease postheparin plasma lipase activities body fat and plasma lipid and lipoprotein concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid profile Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid profile in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
quantitative variation in lipid and lipoprotein traits Gene SetFrom GAD Gene-Disease Associations genes associated with the disease quantitative variation in lipid and lipoprotein traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid variables Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid variables in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cardiovascular disease; lipid metabolism disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cardiovascular disease; lipid metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
bile lipid composition and cholesterol gallstone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease bile lipid composition and cholesterol gallstone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes, type 2; body fat; lipid metabolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes, type 2; body fat; lipid metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
biliary calculi; cholecystolithiasis; gallstones; lipid metabolism disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease biliary calculi; cholecystolithiasis; gallstones; lipid metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma lipid levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma lipid levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
serum lipoprotein lipid and apolipoprotein levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease serum lipoprotein lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease disorder of muscle, unspec; lipid metabolism, inborn errors; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
atherosclerosis, coronary; lipid metabolism disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease atherosclerosis, coronary; lipid metabolism disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
altered lipid oxidation and early insulin secretion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease altered lipid oxidation and early insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
serum lipid levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease serum lipid levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism disorders; muscular diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders; muscular diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
serum lipid parameters Gene SetFrom GAD Gene-Disease Associations genes associated with the disease serum lipid parameters in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease adipose tissue lipoprotein lipase activity and lipoprotein lipid and glucose concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid levels; depression Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid levels; depression in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid response to rosuvastatin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid response to rosuvastatin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma lipid and apolipoprotein levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid response Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid response in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma lipid levels and body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma lipid levels and body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
alzheimer disease; dementia; dementia, vascular; lipid metabolism disorders; neurodegenerative diseases Gene SetFrom GAD Gene-Disease Associations genes associated with the disease alzheimer disease; dementia; dementia, vascular; lipid metabolism disorders; neurodegenerative diseases in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose tolerance; lipid metabolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose tolerance; lipid metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesterol, hdl; blood pressure, arterial; acetaldehyde; lipid peroxide Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesterol, hdl; blood pressure, arterial; acetaldehyde; lipid peroxide in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism disorders; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary heart disease and plasma lipid levels. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary heart disease and plasma lipid levels. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid profiles Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid profiles in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cholesteryl ester transfer protein plasma lipid levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cholesteryl ester transfer protein plasma lipid levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gonadal steroids and lipid levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gonadal steroids and lipid levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease diabetes mellitus type ii; diabetes mellitus, type 2; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
igf-i activity and lipid parameters Gene SetFrom GAD Gene-Disease Associations genes associated with the disease igf-i activity and lipid parameters in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma lipid traits Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma lipid traits in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism, inborn errors; sudden infant death Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism, inborn errors; sudden infant death in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid concentrations Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid concentrations in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
altered lipid levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease altered lipid levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism and adiposity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism and adiposity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid and apolipoprotein levels Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid and apolipoprotein levels in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid metabolism disorders; hyperlipidemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lipid metabolism disorders; hyperlipidemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
coronary disease; coronary heart disease; lipid metabolism, inborn errors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease coronary disease; coronary heart disease; lipid metabolism, inborn errors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lipid Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term lipid in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
positive regulation of lipid storage Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipid storage biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
antigen processing and presentation, endogenous lipid antigen via mhc class ib Gene SetFrom GO Biological Process Annotations 2015 genes participating in the antigen processing and presentation, endogenous lipid antigen via mhc class ib biological process from the curated GO Biological Process Annotations 2015 dataset. |
ether lipid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ether lipid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lipid transport across blood brain barrier Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid glycosylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid glycosylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lipid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid binding Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid binding biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipid binding Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipid binding biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
chemokine receptor transport within lipid bilayer Gene SetFrom GO Biological Process Annotations 2015 genes participating in the chemokine receptor transport within lipid bilayer biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid kinase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid kinase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to lipid Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to lipid biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipid storage Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipid storage biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
membrane lipid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the membrane lipid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
neutral lipid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neutral lipid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid digestion Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid digestion biological process from the curated GO Biological Process Annotations 2015 dataset. |
neutral lipid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neutral lipid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid storage Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid storage biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid translocation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid translocation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid transport across blood brain barrier Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular lipid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular lipid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
antigen processing and presentation of lipid antigen via mhc class ib Gene SetFrom GO Biological Process Annotations 2015 genes participating in the antigen processing and presentation of lipid antigen via mhc class ib biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid transport by regulation of transcription from rna polymerase ii promoter Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid transport by regulation of transcription from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations 2015 dataset. |
multicellular organismal lipid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the multicellular organismal lipid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of intracellular lipid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of intracellular lipid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular lipid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular lipid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid modification Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid modification biological process from the curated GO Biological Process Annotations 2015 dataset. |
intracellular lipid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the intracellular lipid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid particle organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid particle organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein-lipid complex assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein-lipid complex assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein-lipid complex subunit organization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein-lipid complex subunit organization biological process from the curated GO Biological Process Annotations 2015 dataset. |
membrane lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the membrane lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
oligosaccharide-lipid intermediate biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the oligosaccharide-lipid intermediate biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to lipid hydroperoxide Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to lipid hydroperoxide biological process from the curated GO Biological Process Annotations 2015 dataset. |
inositol lipid-mediated signaling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the inositol lipid-mediated signaling biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid storage Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid storage biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid transport by negative regulation of transcription from rna polymerase ii promoter Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid transport by negative regulation of transcription from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
membrane lipid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the membrane lipid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid transport by positive regulation of transcription from rna polymerase ii promoter Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid transport by positive regulation of transcription from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations 2015 dataset. |
response to lipid Gene SetFrom GO Biological Process Annotations 2015 genes participating in the response to lipid biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein transport within lipid bilayer Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein transport within lipid bilayer biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid phosphorylation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid phosphorylation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lipid kinase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipid kinase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid homeostasis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid homeostasis biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lipid metabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipid metabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
ether lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the ether lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of membrane lipid distribution Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of membrane lipid distribution biological process from the curated GO Biological Process Annotations 2015 dataset. |
cellular response to lipid hydroperoxide Gene SetFrom GO Biological Process Annotations 2015 genes participating in the cellular response to lipid hydroperoxide biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid transport across blood brain barrier Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid transport across blood brain barrier biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of intracellular lipid transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of intracellular lipid transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid hydroperoxide transport Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid hydroperoxide transport biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of lipid kinase activity Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of lipid kinase activity biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid localization Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid localization biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid tube assembly Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid tube assembly biological process from the curated GO Biological Process Annotations 2015 dataset. |
lipid oxidation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the lipid oxidation biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein-lipid complex remodeling Gene SetFrom GO Biological Process Annotations 2015 genes participating in the protein-lipid complex remodeling biological process from the curated GO Biological Process Annotations 2015 dataset. |
b cell receptor transport within lipid bilayer Gene SetFrom GO Biological Process Annotations 2015 genes participating in the b cell receptor transport within lipid bilayer biological process from the curated GO Biological Process Annotations 2015 dataset. |
neutral lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the neutral lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of lipid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of lipid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
antigen processing and presentation, exogenous lipid antigen via mhc class ib Gene SetFrom GO Biological Process Annotations 2015 genes participating in the antigen processing and presentation, exogenous lipid antigen via mhc class ib biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of lipid catabolic process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of lipid catabolic process biological process from the curated GO Biological Process Annotations 2015 dataset. |
protein-lipid complex Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the protein-lipid complex cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
lipid particle Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the lipid particle cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
lipid tube Gene SetFrom GO Cellular Component Annotations 2015 proteins localized to the lipid tube cellular component from the curated GO Cellular Component Annotations 2015 dataset. |
protein-lipid complex binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the protein-lipid complex binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
endogenous lipid antigen binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the endogenous lipid antigen binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipid phosphatase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipid phosphatase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipid kinase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipid kinase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
bioactive lipid receptor activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the bioactive lipid receptor activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
exogenous lipid antigen binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the exogenous lipid antigen binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipid transporter activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipid transporter activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipid-transporting atpase activity Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipid-transporting atpase activity molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipid binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipid binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
lipid antigen binding Gene SetFrom GO Molecular Function Annotations 2015 genes performing the lipid antigen binding molecular function from the curated GO Molecular Function Annotations 2015 dataset. |
Lipid metabolism phenotypes Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Lipid metabolism phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Lipid traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Lipid traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
lipid storage disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease lipid storage disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
lipid metabolism disorder Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease lipid metabolism disorder in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
lipid accumulation in hepatocytes Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the lipid accumulation in hepatocytes phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormality of lipid metabolism Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of lipid metabolism phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
increased intramyocellular lipid droplets Gene SetFrom HPO Gene-Disease Associations genes associated with the increased intramyocellular lipid droplets phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased hepatocellular lipid droplets Gene SetFrom HPO Gene-Disease Associations genes associated with the increased hepatocellular lipid droplets phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
lipid accumulation in hepatocytes Gene SetFrom HPO Gene-Disease Associations genes associated with the lipid accumulation in hepatocytes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of lipid metabolism Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of lipid metabolism phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
increased muscle lipid content Gene SetFrom HPO Gene-Disease Associations genes associated with the increased muscle lipid content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Lipid Metabolism, Inborn Errors Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lipid Metabolism, Inborn Errors phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lipid Metabolism Disorders Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Lipid Metabolism Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Lipid-binding serum glycoprotein, conserved site Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid-binding serum glycoprotein, conserved site protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid transport, open beta-sheet Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid transport, open beta-sheet protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
MD-2-related lipid-recognition domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the MD-2-related lipid-recognition domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Tensin phosphatase, lipid phosphatase domain Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Tensin phosphatase, lipid phosphatase domain protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid-binding serum glycoprotein, C-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid-binding serum glycoprotein, C-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid transport protein, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid transport protein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid-binding serum glycoprotein, N-terminal Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid-binding serum glycoprotein, N-terminal protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
StAR-related lipid transfer protein 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the StAR-related lipid transfer protein 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Hypoxia-inducible lipid droplet-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Hypoxia-inducible lipid droplet-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid phosphate phosphatase-related protein type 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid phosphate phosphatase-related protein type 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid phosphate phosphatase-related protein type 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid phosphate phosphatase-related protein type 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid phosphate phosphatase-related protein type 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid phosphate phosphatase-related protein type 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid phosphate phosphatase-related protein type 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid phosphate phosphatase-related protein type 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid phosphate phosphatase-related protein type 4 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid phosphate phosphatase-related protein type 4 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid transport protein, beta-sheet shell Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid transport protein, beta-sheet shell protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
StAR-related lipid transfer protein 5 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the StAR-related lipid transfer protein 5 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid phosphate phosphohydrolase 1 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid phosphate phosphohydrolase 1 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid phosphate phosphohydrolase 2 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid phosphate phosphohydrolase 2 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Lipid phosphate phosphohydrolase 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Lipid phosphate phosphohydrolase 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
ether lipid metabolism Gene SetFrom KEGG Pathways proteins participating in the ether lipid metabolism pathway from the KEGG Pathways dataset. |
lipid particle Gene SetFrom LOCATE Curated Protein Localization Annotations proteins localized to the lipid particle cellular component in low- or high-throughput protein localization assays from the LOCATE Curated Protein Localization Annotations dataset. |
increased white fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brown fat lipid droplet number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat lipid droplet number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased brown fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased brown fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased brown fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased white fat cell lipid droplet size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
neutral lipid storage disease with myopathy Gene SetFrom OMIM Gene-Disease Associations genes associated with the neutral lipid storage disease with myopathy phenotype from the curated OMIM Gene-Disease Associations dataset. |
lipid Gene SetFrom Phosphosite Textmining Biological Term Annotations proteins co-occuring with the biological term lipid in abstracts of publications describing phosphosites from the Phosphosite Textmining Biological Term Annotations dataset. |
Class IB PI3K non-lipid kinase events Gene SetFrom PID Pathways proteins participating in the Class IB PI3K non-lipid kinase events pathway from the PID Pathways dataset. |
HDL-mediated lipid transport Gene Setproteins participating in the HDL-mediated lipid transport pathway from the Reactome Pathways dataset. |
Regulation of lipid metabolism by Peroxisome proliferator-activated receptor alpha (PPARalpha) Gene Setproteins participating in the Regulation of lipid metabolism by Peroxisome proliferator-activated receptor alpha (PPARalpha) pathway from the Reactome Pathways dataset. |
ABCA transporters in lipid homeostasis Gene Setproteins participating in the ABCA transporters in lipid homeostasis pathway from the Reactome Pathways dataset. |
LDL-mediated lipid transport Gene Setproteins participating in the LDL-mediated lipid transport pathway from the Reactome Pathways dataset. |
Digestion of dietary lipid Gene Setproteins participating in the Digestion of dietary lipid pathway from the Reactome Pathways dataset. |
Chylomicron-mediated lipid transport Gene Setproteins participating in the Chylomicron-mediated lipid transport pathway from the Reactome Pathways dataset. |
Peroxisomal lipid metabolism Gene Setproteins participating in the Peroxisomal lipid metabolism pathway from the Reactome Pathways dataset. |
Lipid digestion, mobilization, and transport Gene Setproteins participating in the Lipid digestion, mobilization, and transport pathway from the Reactome Pathways dataset. |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Gene Setproteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein pathway from the Reactome Pathways dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
Nuclear receptors in lipid metabolism and toxicity(Mus musculus) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Nuclear receptors in lipid metabolism and toxicity(Mus musculus) pathway from the WikiPathways Pathways 2014 dataset. |
Nuclear Receptors in Lipid Metabolism and Toxicity(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Nuclear Receptors in Lipid Metabolism and Toxicity(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
Neutral Lipid Storage Disease With Myopathy Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Neutral Lipid Storage Disease With Myopathy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipid Cell Tumor Of Ovary Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipid Cell Tumor Of Ovary in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipid-Rich Breast Carcinoma Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipid-Rich Breast Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Lipid Storage Myopathy Due To Flavin Adenine Dinucleotide Synthetase Deficiency in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Increased Intramyocellular Lipid Droplets Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Intramyocellular Lipid Droplets in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Muscle Lipid Content Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Muscle Lipid Content in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Lipid Metabolism Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Lipid Metabolism in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lipid-Rich Carcinoma Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lipid-Rich Carcinoma in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Increased Hepatocellular Lipid Droplets Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Increased Hepatocellular Lipid Droplets in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Lipid Accumulation In Hepatocytes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Lipid Accumulation In Hepatocytes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
intermembrane lipid transfer Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intermembrane lipid transfer biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid droplet organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid droplet organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid droplet formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid droplet formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
ether lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the ether lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid tube assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid tube assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipid storage Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid storage biological process from the curated GO Biological Process Annotations 2023 dataset. |
membrane lipid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the membrane lipid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid droplet fusion Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid droplet fusion biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid droplet disassembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid droplet disassembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to lipid Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to lipid biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid phosphorylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid phosphorylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipid kinase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid kinase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipid storage Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid storage biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipid transport across blood-brain barrier Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid transport across blood-brain barrier biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid hydroxylation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid hydroxylation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
intracellular lipid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intracellular lipid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid kinase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid kinase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
response to lipid hydroperoxide Gene SetFrom GO Biological Process Annotations 2023 genes participating in the response to lipid hydroperoxide biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein-lipid complex assembly Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein-lipid complex assembly biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to lipid hydroperoxide Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to lipid hydroperoxide biological process from the curated GO Biological Process Annotations 2023 dataset. |
intestinal lipid absorption Gene SetFrom GO Biological Process Annotations 2023 genes participating in the intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
antigen processing and presentation, endogenous lipid antigen via MHC class Ib Gene SetFrom GO Biological Process Annotations 2023 genes participating in the antigen processing and presentation, endogenous lipid antigen via MHC class Ib biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid transport across blood-brain barrier Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid transport across blood-brain barrier biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular response to lipid Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular response to lipid biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid hydroperoxide transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid hydroperoxide transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular lipid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular lipid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipid binding Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid binding biological process from the curated GO Biological Process Annotations 2023 dataset. |
ether lipid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the ether lipid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein localization to lipid droplet Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein localization to lipid droplet biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipid kinase activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid kinase activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipid transporter activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid transporter activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
membrane lipid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the membrane lipid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
inositol lipid-mediated signaling Gene SetFrom GO Biological Process Annotations 2023 genes participating in the inositol lipid-mediated signaling biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid ubiquitination Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid ubiquitination biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of intestinal lipid absorption Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid import into cell Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid import into cell biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of intracellular lipid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of intracellular lipid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid storage Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid storage biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of intestinal lipid absorption Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipid metabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid metabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
antigen processing and presentation, exogenous lipid antigen via MHC class Ib Gene SetFrom GO Biological Process Annotations 2023 genes participating in the antigen processing and presentation, exogenous lipid antigen via MHC class Ib biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid modification Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid modification biological process from the curated GO Biological Process Annotations 2023 dataset. |
oligosaccharide-lipid intermediate biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the oligosaccharide-lipid intermediate biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
cellular lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the cellular lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
membrane lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the membrane lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid localization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid localization biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of lipid localization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of lipid localization biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid translocation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid translocation biological process from the curated GO Biological Process Annotations 2023 dataset. |
neutral lipid catabolic process Gene SetFrom GO Biological Process Annotations 2023 genes participating in the neutral lipid catabolic process biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipid localization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid localization biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid transport across blood-brain barrier Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid transport across blood-brain barrier biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of lipid transporter activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of lipid transporter activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein-lipid complex organization Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein-lipid complex organization biological process from the curated GO Biological Process Annotations 2023 dataset. |
antigen processing and presentation of lipid antigen via MHC class Ib Gene SetFrom GO Biological Process Annotations 2023 genes participating in the antigen processing and presentation of lipid antigen via MHC class Ib biological process from the curated GO Biological Process Annotations 2023 dataset. |
B cell receptor transport within lipid bilayer Gene SetFrom GO Biological Process Annotations 2023 genes participating in the B cell receptor transport within lipid bilayer biological process from the curated GO Biological Process Annotations 2023 dataset. |
chemokine receptor transport within lipid bilayer Gene SetFrom GO Biological Process Annotations 2023 genes participating in the chemokine receptor transport within lipid bilayer biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid transporter activity Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid transporter activity biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of lipid binding Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of lipid binding biological process from the curated GO Biological Process Annotations 2023 dataset. |
protein transport within lipid bilayer Gene SetFrom GO Biological Process Annotations 2023 genes participating in the protein transport within lipid bilayer biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the lipid modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of intracellular lipid transport Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of intracellular lipid transport biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of intestinal lipid absorption Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2023 dataset. |
retrograde trans-synaptic signaling by lipid Gene SetFrom GO Biological Process Annotations 2023 genes participating in the retrograde trans-synaptic signaling by lipid biological process from the curated GO Biological Process Annotations 2023 dataset. |
trans-synaptic signaling by lipid, modulating synaptic transmission Gene SetFrom GO Biological Process Annotations 2023 genes participating in the trans-synaptic signaling by lipid, modulating synaptic transmission biological process from the curated GO Biological Process Annotations 2023 dataset. |
lipid droplet Gene SetFrom GO Cellular Component Annotations 2023 proteins localized to the lipid droplet cellular component from the curated GO Cellular Component Annotations 2023 dataset. |
lipid phosphatase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the lipid phosphatase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
bioactive lipid receptor activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the bioactive lipid receptor activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
exogenous lipid antigen binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the exogenous lipid antigen binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
endogenous lipid antigen binding Gene SetFrom GO Molecular Function Annotations 2023 genes performing the endogenous lipid antigen binding molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
lipid kinase activity Gene SetFrom GO Molecular Function Annotations 2023 genes performing the lipid kinase activity molecular function from the curated GO Molecular Function Annotations 2023 dataset. |
increased brown fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brown fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased white fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased white fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brown fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brown fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased brown fat lipid droplet number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased brown fat lipid droplet number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased white fat cell lipid droplet size Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased white fat cell lipid droplet size phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased brown fat lipid droplet number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased brown fat lipid droplet number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Lipid-associated macrophage(LAM)_Liver_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Lipid-associated macrophage(LAM)_Liver_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Lipid-associated macrophage(LAM)_Lung_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Lipid-associated macrophage(LAM)_Lung_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
SREBF and miR33 in cholesterol and lipid homeostasis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the SREBF and miR33 in cholesterol and lipid homeostasis pathway from the WikiPathways Pathways 2024 dataset. |
Nuclear receptors in lipid metabolism and toxicity Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Nuclear receptors in lipid metabolism and toxicity pathway from the WikiPathways Pathways 2024 dataset. |
Lipid particles composition Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Lipid particles composition pathway from the WikiPathways Pathways 2024 dataset. |
Lipid metabolism pathway Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Lipid metabolism pathway pathway from the WikiPathways Pathways 2024 dataset. |
Lipid metabolism in senescent cells Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Lipid metabolism in senescent cells pathway from the WikiPathways Pathways 2024 dataset. |
Ether lipid biosynthesis Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Ether lipid biosynthesis pathway from the WikiPathways Pathways 2024 dataset. |
ABC transporters in lipid homeostasis Gene Setproteins participating in the ABC transporters in lipid homeostasis pathway from the Reactome Pathways 2024 dataset. |
Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein Gene Setproteins participating in the Biosynthesis of the N-glycan precursor (dolichol lipid-linked oligosaccharide, LLO) and transfer to a nascent protein pathway from the Reactome Pathways 2024 dataset. |
Digestion of dietary lipid Gene Setproteins participating in the Digestion of dietary lipid pathway from the Reactome Pathways 2024 dataset. |
Intestinal lipid absorption Gene Setproteins participating in the Intestinal lipid absorption pathway from the Reactome Pathways 2024 dataset. |
Lipid particle organization Gene Setproteins participating in the Lipid particle organization pathway from the Reactome Pathways 2024 dataset. |
Peroxisomal lipid metabolism Gene Setproteins participating in the Peroxisomal lipid metabolism pathway from the Reactome Pathways 2024 dataset. |
Regulation of lipid metabolism by PPARalpha Gene Setproteins participating in the Regulation of lipid metabolism by PPARalpha pathway from the Reactome Pathways 2024 dataset. |
intermembrane lipid transfer Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intermembrane lipid transfer biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid droplet organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid droplet organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid droplet formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid droplet formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
ether lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the ether lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid tube assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid tube assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipid metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
intracellular lipid transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intracellular lipid transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipid transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipid transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipid storage Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid storage biological process from the curated GO Biological Process Annotations 2025 dataset. |
membrane lipid metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the membrane lipid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid droplet fusion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid droplet fusion biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid droplet disassembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid droplet disassembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid phosphorylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid phosphorylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid storage Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid storage biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipid catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid transport across blood-brain barrier Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid transport across blood-brain barrier biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipid transport across blood-brain barrier Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid transport across blood-brain barrier biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid glycosylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid glycosylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid hydroxylation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid hydroxylation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipid kinase activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipid kinase activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
response to lipid hydroperoxide Gene SetFrom GO Biological Process Annotations 2025 genes participating in the response to lipid hydroperoxide biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein-lipid complex assembly Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein-lipid complex assembly biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to lipid hydroperoxide Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to lipid hydroperoxide biological process from the curated GO Biological Process Annotations 2025 dataset. |
intestinal lipid absorption Gene SetFrom GO Biological Process Annotations 2025 genes participating in the intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2025 dataset. |
antigen processing and presentation, endogenous lipid antigen via MHC class Ib Gene SetFrom GO Biological Process Annotations 2025 genes participating in the antigen processing and presentation, endogenous lipid antigen via MHC class Ib biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid transport across blood-brain barrier Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid transport across blood-brain barrier biological process from the curated GO Biological Process Annotations 2025 dataset. |
cellular response to lipid Gene SetFrom GO Biological Process Annotations 2025 genes participating in the cellular response to lipid biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid hydroperoxide transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid hydroperoxide transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid binding Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid binding biological process from the curated GO Biological Process Annotations 2025 dataset. |
ether lipid metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the ether lipid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein localization to lipid droplet Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein localization to lipid droplet biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of intestinal lipid absorption Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipid kinase activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid kinase activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipid transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
membrane lipid catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the membrane lipid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of intracellular lipid transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of intracellular lipid transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid ubiquitination Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid ubiquitination biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid import into cell Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid import into cell biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of intracellular lipid transport Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of intracellular lipid transport biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipid catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipid storage Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipid storage biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of intestinal lipid absorption Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid droplet fusion Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid droplet fusion biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipid metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
antigen processing and presentation, exogenous lipid antigen via MHC class Ib Gene SetFrom GO Biological Process Annotations 2025 genes participating in the antigen processing and presentation, exogenous lipid antigen via MHC class Ib biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid modification Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid modification biological process from the curated GO Biological Process Annotations 2025 dataset. |
membrane lipid biosynthetic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the membrane lipid biosynthetic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipid localization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipid localization biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipid localization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid localization biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid translocation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid translocation biological process from the curated GO Biological Process Annotations 2025 dataset. |
neutral lipid catabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the neutral lipid catabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid localization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid localization biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipid transport across blood-brain barrier Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipid transport across blood-brain barrier biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of lipid transporter activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of lipid transporter activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of lipoprotein lipid oxidation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of lipoprotein lipid oxidation biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein-lipid complex organization Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein-lipid complex organization biological process from the curated GO Biological Process Annotations 2025 dataset. |
antigen processing and presentation of lipid antigen via MHC class Ib Gene SetFrom GO Biological Process Annotations 2025 genes participating in the antigen processing and presentation of lipid antigen via MHC class Ib biological process from the curated GO Biological Process Annotations 2025 dataset. |
B cell receptor transport within lipid bilayer Gene SetFrom GO Biological Process Annotations 2025 genes participating in the B cell receptor transport within lipid bilayer biological process from the curated GO Biological Process Annotations 2025 dataset. |
chemokine receptor transport within lipid bilayer Gene SetFrom GO Biological Process Annotations 2025 genes participating in the chemokine receptor transport within lipid bilayer biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of lipid transporter activity Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of lipid transporter activity biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of membrane lipid metabolic process Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of membrane lipid metabolic process biological process from the curated GO Biological Process Annotations 2025 dataset. |
protein transport within lipid bilayer Gene SetFrom GO Biological Process Annotations 2025 genes participating in the protein transport within lipid bilayer biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid modification by small protein conjugation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the lipid modification by small protein conjugation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of intestinal lipid absorption Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of intestinal lipid absorption biological process from the curated GO Biological Process Annotations 2025 dataset. |
retrograde trans-synaptic signaling by lipid Gene SetFrom GO Biological Process Annotations 2025 genes participating in the retrograde trans-synaptic signaling by lipid biological process from the curated GO Biological Process Annotations 2025 dataset. |
lipid droplet Gene SetFrom GO Cellular Component Annotations 2025 proteins localized to the lipid droplet cellular component from the curated GO Cellular Component Annotations 2025 dataset. |
lipid phosphatase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the lipid phosphatase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
bioactive lipid receptor activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the bioactive lipid receptor activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
exogenous lipid antigen binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the exogenous lipid antigen binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
endogenous lipid antigen binding Gene SetFrom GO Molecular Function Annotations 2025 genes performing the endogenous lipid antigen binding molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
lipid kinase activity Gene SetFrom GO Molecular Function Annotations 2025 genes performing the lipid kinase activity molecular function from the curated GO Molecular Function Annotations 2025 dataset. |
Lipid storage disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lipid storage disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Lipid metabolism disorder Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Lipid metabolism disorder from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Lipid storage disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Lipid storage disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lipid storage disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lipid storage disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lipid metabolism disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lipid metabolism disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lipid pneumonia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Lipid pneumonia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
lipid-rich carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease lipid-rich carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Breast lipid-rich carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Breast lipid-rich carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Lipid droplet Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores 2025 proteins localized to the Lipid droplet cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset. |
Lipid droplet Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Lipid droplet cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
monolayer-surrounded lipid storage body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the monolayer-surrounded lipid storage body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
organelle-enclosing lipid monolayer Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the organelle-enclosing lipid monolayer cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Lipid proteinosis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Lipid proteinosis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Neutral lipid storage myopathy Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Neutral lipid storage myopathy phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Lysosomal function and lipid metabolism Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Lysosomal function and lipid metabolism assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Intracellular trafficking and lipid signaling regulation Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Intracellular trafficking and lipid signaling regulation assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Steroidogenesis and lipid metabolism Gene SetFrom CM4AI U2OS Cell Map Protein Localization Assemblies proteins comprising Steroidogenesis and lipid metabolism assembly using integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset. |
Lipid traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipid traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hepatic lipid content in extreme obesity Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hepatic lipid content in extreme obesity phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipid metabolism phenotypes Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipid metabolism phenotypes phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipid or lipoprotein levels Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipid or lipoprotein levels phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Disorders of lipid metabolism Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Disorders of lipid metabolism phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipid levels in hepatitis C treatment Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipid levels in hepatitis C treatment phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipid traits (pleiotropy) (HIPO component 2) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipid traits (pleiotropy) (HIPO component 2) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Lipid traits (pleiotropy) (HIPO component 1) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Lipid traits (pleiotropy) (HIPO component 1) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Ether lipid metabolism Gene SetFrom KEGG Pathways 2026 proteins participating in the Ether lipid metabolism pathway from the KEGG Pathways 2026 dataset. |
Lipid and atherosclerosis Gene SetFrom KEGG Pathways 2026 proteins participating in the Lipid and atherosclerosis pathway from the KEGG Pathways 2026 dataset. |
LIPOSOMAL MUC1/PET-LIPID A VACCINE ONT-10 Gene Setinteracting proteins for the LIPOSOMAL MUC1/PET-LIPID A VACCINE ONT-10 drug from theDGIdb Drug Targets 2026 dataset. |
LIPID ENCAPSULATED ANTI-PLK1 SIRNA TKM-PLK1 Gene Setinteracting proteins for the LIPID ENCAPSULATED ANTI-PLK1 SIRNA TKM-PLK1 drug from theDGIdb Drug Targets 2026 dataset. |
TLR-DIRECTED CATIONIC LIPID-DNA COMPLEX JVRS-100 Gene Setinteracting proteins for the TLR-DIRECTED CATIONIC LIPID-DNA COMPLEX JVRS-100 drug from theDGIdb Drug Targets 2026 dataset. |
LIPID NANOPARTICLE ENCAPSULATED OX40L MRNA-2416 Gene Setinteracting proteins for the LIPID NANOPARTICLE ENCAPSULATED OX40L MRNA-2416 drug from theDGIdb Drug Targets 2026 dataset. |
Thyroid hormone metabolism, abnormal Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Thyroid hormone metabolism, abnormal phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
X-linked mental retardation with short stature, hypogonadism and abnormal gait Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the X-linked mental retardation with short stature, hypogonadism and abnormal gait phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Reflex, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Reflex, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Neutrophil Chemotactic Response, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Neutrophil Chemotactic Response, Abnormal from the curated CTD Gene-Disease Associations dataset. |
Thyroid Hormone Metabolism, Abnormal Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Thyroid Hormone Metabolism, Abnormal from the curated CTD Gene-Disease Associations dataset. |
abnormal retinal correspondence Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease abnormal retinal correspondence in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
abnormal splicing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal splicing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ekg, abnormal; brugada syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ekg, abnormal; brugada syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal urogenital development Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal urogenital development in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal fibrin polymerization and thrombophilia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease abnormal fibrin polymerization and thrombophilia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
abnormal Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term abnormal in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
abnormal cannabidiol Gene SetFrom Guide to Pharmacology Chemical Ligands of Receptors receptors of the abnormal cannabidiol ligand (chemical) from the curated Guide to Pharmacology Chemical Ligands of Receptors dataset. |
abnormal eye physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal gallbladder physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal gallbladder physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal intraocular pressure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal intraocular pressure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eating behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eating behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal thrombosis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal thrombosis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal leukocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal leukocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal iris pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal iris pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bone structure Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bone structure phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal serum iron Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal serum iron phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal emotion/affect behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal bleeding Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal bleeding phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal atrioventricular conduction phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair quantity Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair quantity phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal nervous system electrophysiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal male reproductive system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal external genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal external genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal ekg Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal ekg phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal axial skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal immunoglobulin level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal immunoglobulin level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal monocyte count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal monocyte count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neutrophil cell number Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neutrophil cell number phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal facial shape Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal facial shape phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet count Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet count phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
acquired abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the acquired abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glomerular filtration rate phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal eye morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal testosterone level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal testosterone level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal joint morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal joint morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal motor neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal motor neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal biliary tract morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal biliary tract morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal neuron morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal neuron morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal genital system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal genital system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal appendicular skeleton morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal cortical bone morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal cortical bone morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal respiratory system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal respiratory system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal number of teeth Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal number of teeth phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hair pattern Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hair pattern phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal circulating creatinine level Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal circulating creatinine level phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal peripheral nervous system morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal autonomic nervous system physiology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal platelet function Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal platelet function phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal muscle tone Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal muscle tone phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal diaphysis morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal diaphysis morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal spermatogenesis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal spermatogenesis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal hemoglobin Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal hemoglobin phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal internal genitalia Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal internal genitalia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal glucose homeostasis Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal glucose homeostasis phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal renal morphology Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormal renal morphology phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
abnormal dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of hand bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of hand bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone structure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone structure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal branching pattern of the aortic arch Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal branching pattern of the aortic arch phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal maternal serum screening Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal maternal serum screening phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rod and cone electroretinograms Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rod and cone electroretinograms phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal albumin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal albumin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enchondral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enchondral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of vertebrae Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of vertebrae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet membrane protein expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet membrane protein expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondria in muscle tissue Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondria in muscle tissue phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal placental size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal placental size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal central microtubular pair morphology of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal central microtubular pair morphology of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet granules Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet granules phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal subcutaneous fat tissue distribution Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal subcutaneous fat tissue distribution phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lung lobation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lung lobation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal flash visual evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal flash visual evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine phosphate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine phosphate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal drinking behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal drinking behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal fear/anxiety-related behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal fear/anxiety-related behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal corticomedullary differentiation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal corticomedullary differentiation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal humeral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal humeral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delayed hypersensitivity skin test Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delayed hypersensitivity skin test phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein n-linked glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein n-linked glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal echocardiogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal echocardiogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum ferritin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum ferritin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal female reproductive system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal female reproductive system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axial skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axial skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal calcification of the carpal bones Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal calcification of the carpal bones phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal testosterone level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal testosterone level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal speech discrimination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal speech discrimination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal genital system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal genital system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the lower limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the lower limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal liver function tests during pregnancy Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal liver function tests during pregnancy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hypothalamus physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hypothalamus physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal trabecular bone morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal trabecular bone morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal electrophysiology of sinoatrial node origin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal electrophysiology of sinoatrial node origin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metacarpal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metacarpal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal t3/t4 ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal t3/t4 ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris vasculature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris vasculature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal posturing Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal posturing phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal natural killer cell physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal natural killer cell physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal external genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal external genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal immunoglobulin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal immunoglobulin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
congenital abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the congenital abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nervous system electrophysiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nervous system electrophysiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal monocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal monocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrial arrangement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrial arrangement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of ulna Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of ulna phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating renin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating renin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal folds Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal folds phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pancreas size Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pancreas size phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine sodium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine sodium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vestibulo-ocular reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vestibulo-ocular reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral pedicle morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral pedicle morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tendon morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tendon morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal leukocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal leukocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal tarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal tarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spermatogenesis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spermatogenesis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of pituitary gland Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of pituitary gland phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine potassium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine potassium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission at the neuromuscular junction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission at the neuromuscular junction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pupillary light reflex Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pupillary light reflex phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pyramidal signs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pyramidal signs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pigmentation of the oral mucosa Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pigmentation of the oral mucosa phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of incisors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of incisors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal localization of kidney Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal localization of kidney phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal elasticity of skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal elasticity of skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet volume Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet volume phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vas deferens morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vas deferens morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle tone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle tone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lower motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lower motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ciliary motility Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ciliary motility phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular conduction Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular conduction phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metatarsal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metatarsal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal st segment Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal st segment phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sweat homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sweat homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal base Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal base phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pelvis bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pelvis bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sperm morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sperm morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification of the pubic bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification of the pubic bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal isoelectric focusing of serum transferrin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal isoelectric focusing of serum transferrin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hemoglobin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hemoglobin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of bones of the upper limbs Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of bones of the upper limbs phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nasal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nasal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ossification involving the femoral head and neck Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ossification involving the femoral head and neck phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal concentration of calcium in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal concentration of calcium in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal emotion/affect behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal emotion/affect behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal epiphyseal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal epiphyseal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine cytology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine cytology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal palmar dermatoglyphics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal palmar dermatoglyphics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal csf lactate level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal csf lactate level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal joint morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal joint morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral segmentation and fusion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral segmentation and fusion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal internal genitalia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal internal genitalia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal oral glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal oral glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone collagen fibril morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone collagen fibril morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal delivery Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal delivery phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal middle ear reflexes Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal middle ear reflexes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cervical curvature Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cervical curvature phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal mitochondrial shape Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal mitochondrial shape phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal auditory evoked potentials Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal auditory evoked potentials phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal activity of mitochondrial respiratory chain Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal activity of mitochondrial respiratory chain phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal location of ears Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal location of ears phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cns myelination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cns myelination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal synaptic transmission Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal synaptic transmission phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eating behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eating behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal atrioventricular connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal atrioventricular connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ventriculo-arterial connection Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ventriculo-arterial connection phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anterior horn cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anterior horn cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal upper to lower segment ratio Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal upper to lower segment ratio phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal form of the vertebral bodies Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal form of the vertebral bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal biliary tract physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal biliary tract physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine output Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine output phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal blistering of the skin Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal blistering of the skin phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal diaphysis morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal diaphysis morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cholesterol homeostasis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cholesterol homeostasis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine citrate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine citrate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal size of the palpebral fissures Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal size of the palpebral fissures phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair quantity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair quantity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal anatomic location of the heart Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal anatomic location of the heart phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iron deposition in mitochondria Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iron deposition in mitochondria phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of forearm bone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of forearm bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating aldosterone Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating aldosterone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal male germ cell morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal male germ cell morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal circulating creatinine level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal circulating creatinine level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet function Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet function phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal large intestine physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal large intestine physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facial expression Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facial expression phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine chloride concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine chloride concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vascular physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vascular physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal vertebral ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal vertebral ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal renal morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal renal morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal heart morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal heart morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair laboratory examination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair laboratory examination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal retinal pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal retinal pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the palpebral fissure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the palpebral fissure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal lymphocyte count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal lymphocyte count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal conjugate eye movement Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal conjugate eye movement phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal autonomic nervous system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal autonomic nervous system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pulmonary lymphatics Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pulmonary lymphatics phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal pattern of respiration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal pattern of respiration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal protein glycosylation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal protein glycosylation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hair whorl Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hair whorl phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal connection of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal connection of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage collagen Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage collagen phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical stump bleeding Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical stump bleeding phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal social behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal social behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cortical gyration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cortical gyration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal serum iron Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal serum iron phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of permanent teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of permanent teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sex determination Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sex determination phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal prolactin level Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal prolactin level phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory system morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory system morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of teeth Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of teeth phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory epithelium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory epithelium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal axonemal organization of respiratory motile cilia Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal axonemal organization of respiratory motile cilia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal foot bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal foot bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal neutrophil cell number Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal neutrophil cell number phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal platelet count Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal platelet count phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal eye morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal eye morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cone-mediated electroretinogram Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cone-mediated electroretinogram phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal basal ganglia mri signal intensity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal basal ganglia mri signal intensity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sensory nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sensory nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal muscle glycogen content Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal muscle glycogen content phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal appendicular skeleton morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal appendicular skeleton morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal hand bone ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal hand bone ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal number of erythroid precursors Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal number of erythroid precursors phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal respiratory motile cilium physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal respiratory motile cilium physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urine magnesium concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urine magnesium concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rapid eye movement (rem) sleep Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rapid eye movement (rem) sleep phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal nerve conduction velocity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal nerve conduction velocity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal thrombosis Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal thrombosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glucose tolerance Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glucose tolerance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ekg Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ekg phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal levels of creatine kinase in blood Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal levels of creatine kinase in blood phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal ejaculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal ejaculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal aggressive, impulsive or violent behavior Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal aggressive, impulsive or violent behavior phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal motor neuron morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal motor neuron morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary electrolyte concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary electrolyte concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal finger flexion creases Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal finger flexion creases phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal trabeculation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal trabeculation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal umbilical cord blood vessels Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal umbilical cord blood vessels phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal head movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal head movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
acquired abnormal hair pattern Gene SetFrom HPO Gene-Disease Associations genes associated with the acquired abnormal hair pattern phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal facility in opposing the shoulders Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal facility in opposing the shoulders phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal migration of corneal endothelium Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal migration of corneal endothelium phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal gallbladder physiology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal gallbladder physiology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal intraocular pressure Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal intraocular pressure phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the frontal region Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the frontal region phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal iris pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal iris pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal urinary sulfate concentration Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal urinary sulfate concentration phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal spatial orientation of the cardiac segments Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal spatial orientation of the cardiac segments phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal morphology of the radius Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal morphology of the radius phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal rib ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal rib ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal glomerular filtration rate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal glomerular filtration rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal sternal ossification Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal sternal ossification phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal shape of the occiput Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal shape of the occiput phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal involuntary eye movements Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal involuntary eye movements phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal metaphyseal vascular invasion Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal metaphyseal vascular invasion phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal enzyme/coenzyme activity Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal enzyme/coenzyme activity phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal cartilage morphology Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal cartilage morphology phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormal peripheral action potential amplitude Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormal peripheral action potential amplitude phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Reflex, Abnormal Gene SetFrom HuGE Navigator Gene-Phenotype Associations genes associated with the Reflex, Abnormal phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset. |
Spindle assembly abnormal protein 6 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Spindle assembly abnormal protein 6 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
DMRT/protein doublesex/protein male abnormal 3 Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the DMRT/protein doublesex/protein male abnormal 3 protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Protein male abnormal 21-related Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Protein male abnormal 21-related protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
Abnormal spindle-like microcephaly-associated protein Gene SetFrom InterPro Predicted Protein Domain Annotations proteins predicted to have the Abnormal spindle-like microcephaly-associated protein protein domain from the InterPro Predicted Protein Domain Annotations dataset. |
abnormal clitoris morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal clitoris morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male genitalia morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male genitalia morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lung volume Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lung volume phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basilar membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basilar membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural fold elevation formation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural fold elevation formation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensory capabilities/reflexes/nociception Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensory capabilities/reflexes/nociception phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to anesthetic Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to anesthetic phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal trigeminal ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal trigeminal ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response waveform shape Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response waveform shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal photoreceptor layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal photoreceptor layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bradykinin level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bradykinin level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal fetal derived definitive erythrocyte cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal fetal derived definitive erythrocyte cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paravertebral ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paravertebral ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasal cavity morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasal cavity morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primary sex determination Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primary sex determination phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus stratum lacunosum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus stratum lacunosum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gallbladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gallbladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ectomesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ectomesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male urethra morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male urethra morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone marrow cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone marrow cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zona glomerulosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zona glomerulosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal surfactant secretion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal surfactant secretion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum fastigial nucleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum fastigial nucleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal social/conspecific interaction Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal social/conspecific interaction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hippocampus size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hippocampus size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tooth morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tooth morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neutrophil differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neutrophil differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vomer bone morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vomer bone morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal endplate potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal endplate potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sagittal suture morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sagittal suture morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal semicircular canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal semicircular canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal estrous cycle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal estrous cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive t cell differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive t cell differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neuron differentiation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neuron differentiation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal long bone metaphysis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal long bone metaphysis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal testis size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal testis size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vascular endothelial cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vascular endothelial cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sympathetic neuron innervation pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sympathetic neuron innervation pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanosome transport Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanosome transport phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inferior colliculus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inferior colliculus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tongue muscle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tongue muscle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal inner nuclear layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal inner nuclear layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal behavioral response to methamphetamine Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal behavioral response to methamphetamine phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory brainstem response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory brainstem response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal macrophage derived foam cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal macrophage derived foam cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart left atrium weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart left atrium weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal malleus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal malleus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala vestibuli morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala vestibuli morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pupillary reflex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pupillary reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal interdigital cell death Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal interdigital cell death phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal schwann cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal schwann cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior definitive endoderm morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior definitive endoderm morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal keratinocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal keratinocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal protein reabsorption Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal protein reabsorption phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal habenula morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal habenula morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine antidiuretic hormone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine antidiuretic hormone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryonic tissue morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryonic tissue morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal laryngeal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal laryngeal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasma membrane morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasma membrane morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating angiotensinogen level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating angiotensinogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal corneocyte envelope morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal corneocyte envelope morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal primordial ovarian follicle number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal primordial ovarian follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal prostate gland dorsolateral lobe morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal prostate gland dorsolateral lobe morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular nerve morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular nerve morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal melanocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parametrial fat pad morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parametrial fat pad morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal effector t cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal effector t cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine aldosterone level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine aldosterone level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal roof plate morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal roof plate morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal bone healing Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal bone healing phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rhombomere 4 morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rhombomere 4 morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal heart right ventricle size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal heart right ventricle size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal snout morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal snout morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic disc morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic disc morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parasympathetic ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parasympathetic ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal blinking Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal blinking phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellar molecular layer Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellar molecular layer phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating interleukin-1 alpha level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating interleukin-1 alpha level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thyroid gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thyroid gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal efferent ductules of testis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal efferent ductules of testis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal periocular mesenchyme morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal periocular mesenchyme morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating pancreatic peptide level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating pancreatic peptide level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal frontonasal prominence morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal frontonasal prominence morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal gas homeostasis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal gas homeostasis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intestinal mucosa morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intestinal mucosa morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis papillary layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis papillary layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair shaft morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair shaft morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cellular replicative senescence Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cellular replicative senescence phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal throat morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal throat morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal nasolacrimal duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal nasolacrimal duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal first pharyngeal arch morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal first pharyngeal arch morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal loop of henle descending limb morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal loop of henle descending limb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal triiodothyronine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal triiodothyronine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal visual acuity Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal visual acuity phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating sulfate level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating sulfate level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal parturition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal parturition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal scala tympani morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal scala tympani morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal external urethral orifice morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal external urethral orifice morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal male reproductive gland physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal male reproductive gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal chorioallantoic fusion Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal chorioallantoic fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal purkinje cell dendrite morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal purkinje cell dendrite morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lens development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lens development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pituitary diverticulum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pituitary diverticulum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal arteriole morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal arteriole morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal outer hair cell stereociliary bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic endocrine progenitor cell proliferation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic endocrine progenitor cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cd4-positive, cd25-positive, alpha-beta regulatory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rosenthal canal morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rosenthal canal morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal enterocyte apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal enterocyte apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal glomerulus basement membrane thickness Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal glomerulus basement membrane thickness phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal superior vagus ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal superior vagus ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal melanoblast morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal melanoblast morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder weight Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal single cell response threshold Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal single cell response threshold phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal dermis reticular layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal dermis reticular layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal body height Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal body height phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelial cell primary cilium physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelial cell primary cilium physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal optic stalk morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal optic stalk morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural tube mantle layer morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural tube mantle layer morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal posterior cardinal vein morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal posterior cardinal vein morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal renal tubule epithelial cell primary cilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal renal tubule epithelial cell primary cilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal intramembranous bone ossification Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal intramembranous bone ossification phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal ear distance/ position Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal ear distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mitochondrion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mitochondrion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal maxillary sinus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal maxillary sinus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal otic vesicle development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal otic vesicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brown adipose tissue physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brown adipose tissue physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lymph node b cell domain morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lymph node b cell domain morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating lactate dehydrogenase level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating lactate dehydrogenase level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal plasmacytoid dendritic cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal plasmacytoid dendritic cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urinary bladder morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urinary bladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal rod cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal rod cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal digestive system development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal digestive system development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auditory summating potential Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auditory summating potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal paired-pulse inhibition Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal paired-pulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal aortic arch and aortic arch branch attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal aortic arch and aortic arch branch attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal retinal ganglion cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal retinal ganglion cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal postnatal growth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal postnatal growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal brain development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal brain development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal memory t cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal memory t cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal miniature inhibitory postsynaptic currents Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal miniature inhibitory postsynaptic currents phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal osteocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal osteocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal axillary lymph node morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal axillary lymph node morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal costal cartilage morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal costal cartilage morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal splenocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal splenocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal circulating chemokine level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal circulating chemokine level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum posterior vermis morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum posterior vermis morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal thalamus morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal thalamus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair medulla air spaces Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair medulla air spaces phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal zigzag hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal zigzag hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal xenobiotic induced morbidity/mortality Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal xenobiotic induced morbidity/mortality phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney epithelium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney epithelium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pons morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pons morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b cell anergy Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b cell anergy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal rr interval Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal rr interval phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somite size Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somite size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pancreatic acinar cell zymogen granule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pancreatic acinar cell zymogen granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal meibomian gland development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal meibomian gland development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal basophil physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal basophil physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cerebellum vermis lobule ii morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cerebellum vermis lobule ii morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tubuloglomerular feedback response Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tubuloglomerular feedback response phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal b wave amplitude Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal b wave amplitude phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal urine organic cation level Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal urine organic cation level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal embryo attachment Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal embryo attachment phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal myogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal myogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal eye morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal eye morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal kidney collecting duct morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal kidney collecting duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal olfactory bulb granule cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal olfactory bulb granule cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal lumbar dorsal root ganglion morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal lumbar dorsal root ganglion morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sensorimotor gating Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sensorimotor gating phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal somatic sensory system morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal somatic sensory system morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal coccygeal vertebrae morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal coccygeal vertebrae morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cell chemotaxis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cell chemotaxis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal neural crest cell apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal neural crest cell apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal axon pruning Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal axon pruning phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pinna reflex Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pinna reflex phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal glomerular capillary morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal glomerular capillary morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hind foot hair pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hind foot hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal spinal cord dorsal column morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal spinal cord dorsal column morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal coronary vessel morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal coronary vessel morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal mucous neck cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal mucous neck cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pre-pro b cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pre-pro b cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal sertoli cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal sertoli cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |