| Name |
|---|
BDLN1 Genebody length, human homolog of mouse body length 1 |
CHMP1B Genecharged multivesicular body protein 1B CHMP1B belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008] |
CHMP3 Genecharged multivesicular body protein 3 This gene encodes a protein that sorts transmembrane proteins into lysosomes/vacuoles via the multivesicular body (MVB) pathway. This protein, along with other soluble coiled-coil containing proteins, forms part of the ESCRT-III protein complex that binds to the endosomal membrane and recruits additional cofactors for protein sorting into the MVB. This protein may also co-immunoprecipitate with a member of the IFG-binding protein superfamily. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ring finger protein 103 (RNF103) gene. [provided by RefSeq, Nov 2010] |
CHMP7 Genecharged multivesicular body protein 7 Involved in several processes, including midbody abscission; mitotic nuclear division; and vacuolar transport. Located in chromatin; cytosol; and nucleus. Part of several cellular components, including bounding membrane of organelle; kinetochore microtubule; and midbody. [provided by Alliance of Genome Resources, Mar 2025] |
CHMP5 Genecharged multivesicular body protein 5 CHMP5 belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008] |
CHMP4A Genecharged multivesicular body protein 4A CHMP4A belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008] |
CHMP4B Genecharged multivesicular body protein 4B This gene encodes a member of the chromatin-modifying protein/charged multivesicular body protein (CHMP) protein family. The protein is part of the endosomal sorting complex required for transport (ESCRT) complex III (ESCRT-III), which functions in the sorting of endocytosed cell-surface receptors into multivesicular endosomes. The ESCRT machinery also functions in the final abscisson stage of cytokinesis and in the budding of enveloped viruses such as HIV-1. The three proteins of the CHMP4 subfamily interact with programmed cell death 6 interacting protein (PDCD6IP, also known as ALIX), which also functions in the ESCRT pathway. The CHMP4 proteins assemble into membrane-attached 5-nm filaments that form circular scaffolds and promote or stabilize outward budding. These polymers are proposed to help generate the luminal vesicles of multivesicular bodies. Mutations in this gene result in autosomal dominant posterior polar cataracts.[provided by RefSeq, Oct 2009] |
CHMP4C Genecharged multivesicular body protein 4C CHMP4C belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008] |
LOC100130209 Genecharged multivesicular body protein 4A pseudogene |
SP140L GeneSP140 nuclear body protein-like Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Mar 2025] |
BMIQ8 Genebody mass index quantitative trait locus 8 |
BMIQ6 Genebody mass index QTL 6 |
BMIQ5 Genebody mass index QTL 5 |
BMIQ2 Genebody mass index QTL 2 |
BMIQ3 Genebody mass index QTL 3 |
BMIQ1 Genebody mass index QTL 1 |
CHMP6 Genecharged multivesicular body protein 6 This gene encodes a member of the chromatin-modifying protein/charged multivesicular body protein family. Proteins in this family are part of the ESCRT-III (endosomal sorting complex required for transport III) which degrades surface receptors, and in biosynthesis of endosomes. [provided by RefSeq, Mar 2012] |
BW1 GeneBody weight QTL 1 |
BW2 GeneBody weight QTL 2 |
BW3 GeneBody weight QTL 3 |
BW4 GeneBody weight QTL 4 |
BW6 GeneBody weight QTL 6 |
BW7 GeneBody weight QTL 7 |
BW8 GeneBody weight QTL 8 |
BW9 GeneBody weight QTL 9 |
BW27 GeneBody weight QTL 27 |
BW26 GeneBody weight QTL 26 |
BW24 GeneBody weight QTL 24 |
BW23 GeneBody weight QTL 23 |
BW22 GeneBody weight QTL 22 |
BW20 GeneBody weight QTL 20 |
BW29 GeneBody weight QTL 29 |
BW28 GeneBody weight QTL 28 |
BMIQ14 GeneBody mass index QTL14 |
BMIQ15 GeneBody mass index QTL 15 |
BFD1 GeneBody fluid distribution QTL 1 |
BFD3 GeneBody fluid distribution QTL 3 |
BFD4 GeneBody fluid distribution QTL 4 |
BFD5 GeneBody fluid distribution QTL 5 |
CHMP1A Genecharged multivesicular body protein 1A This gene encodes a member of the CHMP/Chmp family of proteins which are involved in multivesicular body sorting of proteins to the interiors of lysosomes. The initial prediction of the protein sequence encoded by this gene suggested that the encoded protein was a metallopeptidase. The nomenclature has been updated recently to reflect the correct biological function of this encoded protein. Several transcripts encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2012] |
BW56 GeneBody weight QTL 56 |
BW57 GeneBody weight QTL 57 |
BW54 GeneBody weight QTL 54 |
BW55 GeneBody weight QTL 55 |
BW52 GeneBody weight QTL 52 |
BW53 GeneBody weight QTL 53 |
BW58 GeneBody weight QTL 58 |
BW59 GeneBody weight QTL 59 |
CHMP2B Genecharged multivesicular body protein 2B This gene encodes a component of the heteromeric ESCRT-III complex (Endosomal Sorting Complex Required for Transport III) that functions in the recycling or degradation of cell surface receptors. ESCRT-III functions in the concentration and invagination of ubiquitinated endosomal cargos into intralumenal vesicles. The protein encoded by this gene is found as a monomer in the cytosol or as an oligomer in ESCRT-III complexes on endosomal membranes. It is expressed in neurons of all major regions of the brain. Mutations in this gene result in one form of familial frontotemporal lobar degeneration. [provided by RefSeq, Jul 2008] |
CHMP2A Genecharged multivesicular body protein 2A CHMP2A belongs to the chromatin-modifying protein/charged multivesicular body protein (CHMP) family. These proteins are components of ESCRT-III (endosomal sorting complex required for transport III), a complex involved in degradation of surface receptor proteins and formation of endocytic multivesicular bodies (MVBs). Some CHMPs have both nuclear and cytoplasmic/vesicular distributions, and one such CHMP, CHMP1A (MIM 164010), is required for both MVB formation and regulation of cell cycle progression (Tsang et al., 2006 [PubMed 16730941]).[supplied by OMIM, Mar 2008] |
LOC100420338 Genecharged multivesicular body protein 5 pseudogene |
LBMQTL1 GeneLean body mass QTL 1 |
SCARNA27 Genesmall Cajal body-specific RNA 27 |
SCARNA22 Genesmall Cajal body-specific RNA 22 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA23 Genesmall Cajal body-specific RNA 23 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA20 Genesmall Cajal body-specific RNA 20 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA21 Genesmall Cajal body-specific RNA 21 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
CHMP4BP1 Genecharged multivesicular body protein 4B pseudogene 1 Predicted to be involved in late endosome to vacuole transport via multivesicular body sorting pathway and vesicle budding from membrane. Predicted to be located in several cellular components, including bounding membrane of organelle; kinetochore microtubule; and midbody. Predicted to be part of ESCRT III complex. Predicted to be active in cytoplasmic side of plasma membrane and multivesicular body. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA5 Genesmall Cajal body-specific RNA 5 Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA4 Genesmall Cajal body-specific RNA 4 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA2 Genesmall Cajal body-specific RNA 2 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
BW15 GeneBody weight QTL 15 |
BW36 GeneBody weight QTL 36 |
BW37 GeneBody weight QTL 37 |
BW88 GeneBody weight QTL 88 |
VTA1P2 Genevesicle (multivesicular body) trafficking 1 pseudogene 2 |
NOLC1 Genenucleolar and coiled-body phosphoprotein 1 Enables molecular function inhibitor activity; protein heterodimerization activity; and protein-macromolecule adaptor activity. Involved in neural crest cell development; neural crest formation; and regulation of translation. Acts upstream of or within axonogenesis and regulation of synaptic plasticity. Located in fibrillar center. [provided by Alliance of Genome Resources, Mar 2025] |
BW35 GeneBody weight QTL 35 |
BW30 GeneBody weight QTL 30 |
BW33 GeneBody weight QTL 33 |
MHB Genemyopathy, hyaline body, autosomal recessive |
BW5 GeneBody weight QTL 5 |
BMIQ13 GeneBody mass index QTL13 |
LOC100420317 Genecharged multivesicular body protein 5 pseudogene |
BW25 GeneBody weight QTL 25 |
LOC392426 Genenucleolar and coiled-body phosphoprotein 1 pseudogene |
BW69 GeneBody weight QTL 69 |
BW68 GeneBody weight QTL 68 |
BW63 GeneBody weight QTL 63 |
BW62 GeneBody weight QTL 62 |
BW61 GeneBody weight QTL 61 |
BW60 GeneBody weight QTL 60 |
BW67 GeneBody weight QTL 67 |
BW66 GeneBody weight QTL 66 |
BW65 GeneBody weight QTL 65 |
BW64 GeneBody weight QTL 64 |
BW11 GeneBody weight QTL 11 |
SCARNA9L Genesmall Cajal body-specific RNA 9-like Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
BFD2 GeneBody fluid distribution QTL 2 |
SCARNA13 Genesmall Cajal body-specific RNA 13 Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA12 Genesmall Cajal body-specific RNA 12 This gene produces a small nuclear RNA that localizes specifically to Cajal bodies, which are conserved subnuclear organelles that are present in the nucleoplasm. This RNA is processed from an intron of the prohibitin 2 host gene. It includes both an H/ACA box and a C/D box, and is thought to guide the pseudouridylation of residue U46 in the U5 small nuclear RNA. [provided by RefSeq, Jun 2010] |
SCARNA11 Genesmall Cajal body-specific RNA 11 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA10 Genesmall Cajal body-specific RNA 10 Predicted to be involved in RNA processing. Located in Cajal body. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA17 Genesmall Cajal body-specific RNA 17 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA16 Genesmall Cajal body-specific RNA 16 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA15 Genesmall Cajal body-specific RNA 15 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. Predicted to be part of RISC complex. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA14 Genesmall Cajal body-specific RNA 14 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA18 Genesmall Cajal body-specific RNA 18 Small nucleolar RNAs (snoRNAs) are small noncoding RNAs involved in RNA processing. Box H/ACA snoRNAs, such as SCARNA18, direct the conversion of uridine to pseudouridine at specific residues of ribosomal RNAs or small nuclear RNAs (snRNAs) (Gu et al., 2005).[supplied by OMIM, Mar 2008] |
VTA1 Genevesicle (multivesicular body) trafficking 1 C6ORF55 encodes a protein involved in trafficking of the multivesicular body, an endosomal compartment involved in sorting membrane proteins for degradation in lysosomes (Ward et al., 2005 [PubMed 15644320]).[supplied by OMIM, Mar 2008] |
SCARNA9 Genesmall Cajal body-specific RNA 9 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA8 Genesmall Cajal body-specific RNA 8 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA7 Genesmall Cajal body-specific RNA 7 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA3 Genesmall Cajal body-specific RNA 3 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
SCARNA1 Genesmall Cajal body-specific RNA 1 Predicted to be involved in RNA processing. Predicted to be located in Cajal body and nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
BW12 GeneBody weight QTL 12 |
BW13 GeneBody weight QTL 13 |
BW10 GeneBody weight QTL 10 |
BW16 GeneBody weight QTL 16 |
BW17 GeneBody weight QTL 17 |
BW14 GeneBody weight QTL 14 |
BW18 GeneBody weight QTL 18 |
BW19 GeneBody weight QTL 19 |
CHMP1AP1 Genecharged multivesicular body protein 1A pseudogene 1 |
LOC100129367 Genenucleolar and coiled-body phosphoprotein 1 pseudogene |
CHMP1B2P Genecharged multivesicular body protein 1B2, pseudogene |
PARK3 GeneParkinson disease 3 (autosomal dominant, Lewy body) |
SP140 GeneSP140 nuclear body protein This gene encodes a member of the SP100 family of proteins, which are share common domains including an N-terminal homogeneously staining region domain followed by a SP100/autoimmune regulator/NucP41/P75/deformed epidermal autoregulatory factor domain, a plant homeobox zinc finger, and a bromodomain. The encoded protein is interferon-inducible and is expressed at high levels in the nuclei of leukocytes. Variants of this gene have been associated with multiple sclerosis, Crohn's disease, and chronic lymphocytic leukemia. Alternative splicing results in multiple variants. [provided by RefSeq, Aug 2016] |
BW34 GeneBody weight QTL 34 |
BW31 GeneBody weight QTL 31 |
BW32 GeneBody weight QTL 32 |
SCARNA6 Genesmall Cajal body-specific RNA 6 Predicted to be involved in RNA processing. Predicted to be located in nucleolus. [provided by Alliance of Genome Resources, Mar 2025] |
MVB12B Genemultivesicular body subunit 12B The protein encoded by this gene is a component of the ESCRT-I complex, a heterotetramer, which mediates the sorting of ubiquitinated cargo protein from the plasma membrane to the endosomal vesicle. ESCRT-I complex plays an essential role in HIV budding and endosomal protein sorting. Depletion and overexpression of this and related protein (MVB12A) inhibit HIV-1 infectivity and induce unusual viral assembly defects, indicating a role for MVB12 subunits in regulating ESCRT-mediated virus budding. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011] |
MVB12A Genemultivesicular body subunit 12A Enables lipid binding activity and ubiquitin binding activity. Involved in regulation of epidermal growth factor receptor signaling pathway. Located in several cellular components, including centrosome; cytosol; and vesicle. Part of ESCRT I complex. [provided by Alliance of Genome Resources, Mar 2025] |
SP110 GeneSP110 nuclear body protein The nuclear body is a multiprotein complex that may have a role in the regulation of gene transcription. This gene is a member of the SP100/SP140 family of nuclear body proteins and encodes a leukocyte-specific nuclear body component. The protein can function as an activator of gene transcription and may serve as a nuclear hormone receptor coactivator. In addition, it has been suggested that the protein may play a role in ribosome biogenesis and in the induction of myeloid cell differentiation. Alternative splicing has been observed for this gene and three transcript variants, encoding distinct isoforms, have been identified. [provided by RefSeq, Jul 2008] |
BW70 GeneBody weight QTL 70 |
BW71 GeneBody weight QTL 71 |
BW72 GeneBody weight QTL 72 |
NBDY Genenegative regulator of P-body association Involved in negative regulation of cytoplasmic mRNA processing body assembly and nuclear-transcribed mRNA catabolic process. Located in P-body. [provided by Alliance of Genome Resources, Mar 2025] |
BBOF1 Genebasal body orientation factor 1 Predicted to be involved in sperm axoneme assembly. Predicted to act upstream of or within several processes, including cilium movement involved in cell motility; negative regulation of microtubule depolymerization; and protein stabilization. Predicted to be located in axoneme; ciliary basal body; and sperm flagellum. [provided by Alliance of Genome Resources, Mar 2025] |
sparse body hair Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse body hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
Sparse Body Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Body Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
sparse scalp hair Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse scalp hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse hair Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse facial hair Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse facial hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse pubic hair Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse pubic hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse axillary hair Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse axillary hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sparse hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Sparse Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse Scalp Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Scalp Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse Axillary Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Axillary Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse Pubic Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Pubic Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse Anterior Scalp Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Anterior Scalp Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
sparse hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the sparse hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Sparse hair Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Sparse hair phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
sparse Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term sparse in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
sparse lateral eyebrow Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse lateral eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse bone trabeculae Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse bone trabeculae phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse eyelashes Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse or absent eyelashes Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse or absent eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse lower eyelashes Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse lower eyelashes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse eyebrow Gene SetFrom HPO Gene-Disease Associations genes associated with the sparse eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
sparse vibrissae Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the sparse vibrissae phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
Sparse Eyebrow Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Eyebrow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse Eyelashes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse And Thin Eyebrow Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse And Thin Eyebrow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse Or Absent Eyelashes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Or Absent Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse Bone Trabeculae Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Bone Trabeculae in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse Lateral Eyebrow Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Lateral Eyebrow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Sparse Lower Eyelashes Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Sparse Lower Eyelashes in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
sparse vibrissae Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the sparse vibrissae phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
[skin/hair/eye pigmentation 6, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 6, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 9, dark/light hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 9, dark/light hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 10, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 10, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[hair morphology 1, hair thickness] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [hair morphology 1, hair thickness] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, black/nonblack hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, black/nonblack hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 2, red hair/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 2, red hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 7, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 7, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 2, blond hair/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 2, blond hair/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 11 (melanesian blond hair)] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 1, blond/brown hair] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 1, blond/brown hair] phenotype from the curated OMIM Gene-Disease Associations dataset. |
establishment of body hair planar orientation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the establishment of body hair planar orientation biological process from the curated GO Biological Process Annotations 2015 dataset. |
establishment of body hair or bristle planar orientation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the establishment of body hair or bristle planar orientation biological process from the curated GO Biological Process Annotations 2015 dataset. |
Premature Graying Of Body Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Premature Graying Of Body Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
establishment of body hair planar orientation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the establishment of body hair planar orientation biological process from the curated GO Biological Process Annotations 2023 dataset. |
establishment of body hair or bristle planar orientation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the establishment of body hair or bristle planar orientation biological process from the curated GO Biological Process Annotations 2023 dataset. |
establishment of body hair planar orientation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the establishment of body hair planar orientation biological process from the curated GO Biological Process Annotations 2025 dataset. |
establishment of body hair or bristle planar orientation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the establishment of body hair or bristle planar orientation biological process from the curated GO Biological Process Annotations 2025 dataset. |
body mass; diabetes, type 2; insulin; glucose; body fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; insulin; glucose; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; body fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
decreased percent body fat/body weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased percent body fat/body weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased percent body fat/body weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased percent body fat/body weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal percent body fat/body weight Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal percent body fat/body weight phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
Skin/hair/eye pigmentation, variation in, 1 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 8 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Woolly hair, autosomal recessive 2, with or without hypotrichosis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Woolly hair, autosomal recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 4 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 5 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 9 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 10 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin/hair/eye pigmentation, variation in, 11 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin/hair/eye pigmentation, variation in, 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy dilated with woolly hair and keratoderma Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy dilated with woolly hair and keratoderma phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Menkes kinky-hair syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Menkes kinky-hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Skin fragility woolly hair syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Skin fragility woolly hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
root hair tip Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the root hair tip cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cell hair Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cell hair cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
root hair Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the root hair cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Hair Dyes Gene SetFrom CTD Gene-Chemical Interactions genes/proteins interacting with the chemical Hair Dyes from the curated CTD Gene-Chemical Interactions dataset. |
TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease TRICHOTHIODYSTROPHY, PHOTOSENSITIVE;TTDP ICHTHYOSIFORM ERYTHRODERMA WITH HAIR ABNORMALITY AND MENTAL AND GROWTH from the curated CTD Gene-Disease Associations dataset. |
WOOLLY HAIR, AUTOSOMAL DOMINANT Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease WOOLLY HAIR, AUTOSOMAL DOMINANT from the curated CTD Gene-Disease Associations dataset. |
Menkes Kinky Hair Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Menkes Kinky Hair Syndrome from the curated CTD Gene-Disease Associations dataset. |
Hair Diseases Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Hair Diseases from the curated CTD Gene-Disease Associations dataset. |
Cartilage-hair hypoplasia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cartilage-hair hypoplasia from the curated CTD Gene-Disease Associations dataset. |
Skin Fragility-Woolly Hair Syndrome Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Skin Fragility-Woolly Hair Syndrome from the curated CTD Gene-Disease Associations dataset. |
Cardiomyopathy dilated with Woolly hair and keratoderma Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Cardiomyopathy dilated with Woolly hair and keratoderma from the curated CTD Gene-Disease Associations dataset. |
NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease NOONAN SYNDROME-LIKE DISORDER WITH LOOSE ANAGEN HAIR from the curated CTD Gene-Disease Associations dataset. |
ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE from the curated CTD Gene-Disease Associations dataset. |
Woolly hair, congenital Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Woolly hair, congenital from the curated CTD Gene-Disease Associations dataset. |
Hair Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Hair in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Hair Color Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Hair Color in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
hair disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hair disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hair follicle neoplasm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores genes involed in the disease hair follicle neoplasm from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset. |
hair disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores genes associated with the disease hair disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset. |
hair follicle neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hair follicle neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
cartilage-hair hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease cartilage-hair hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
hair disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease hair disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
black vs red hair color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease black vs red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hair color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
ultrastructure of the hair Gene SetFrom GAD Gene-Disease Associations genes associated with the disease ultrastructure of the hair in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hair thickness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hair thickness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
red vs non-red hair color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease red vs non-red hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
black vs blond hair color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease black vs blond hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
straight hair Gene SetFrom GAD Gene-Disease Associations genes associated with the disease straight hair in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
blond vs brown hair color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease blond vs brown hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hair morphology Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hair morphology in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hair Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hair in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hair colour Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hair colour in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
cutaneous melanoma which is largely independent of skin type and hair color Gene SetFrom GAD Gene-Disease Associations genes associated with the disease cutaneous melanoma which is largely independent of skin type and hair color in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hair Gene SetFrom GeneRIF Biological Term Annotations genes co-occuring with the biological term hair in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset. |
negative regulation of hair follicle maturation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair follicle placode formation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair follicle placode formation biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair follicle development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair follicle development biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of root hair elongation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of root hair elongation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of root hair elongation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of root hair elongation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of hair cycle by canonical wnt signaling pathway Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of hair cycle by canonical wnt signaling pathway biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of hair cycle Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of hair cycle biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of hair follicle maturation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair cycle phase Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair cycle phase biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair cell differentiation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair cell differentiation biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of hair follicle development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of hair follicle development biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of hair follicle cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair cycle process Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair cycle process biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of hair follicle cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of hair cycle Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of hair cycle biological process from the curated GO Biological Process Annotations 2015 dataset. |
regulation of hair cycle Gene SetFrom GO Biological Process Annotations 2015 genes participating in the regulation of hair cycle biological process from the curated GO Biological Process Annotations 2015 dataset. |
negative regulation of hair follicle development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the negative regulation of hair follicle development biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of hair follicle development Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of hair follicle development biological process from the curated GO Biological Process Annotations 2015 dataset. |
positive regulation of hair follicle maturation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the positive regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair follicle morphogenesis Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair follicle morphogenesis biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair cycle Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair cycle biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair follicle cell proliferation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2015 dataset. |
hair follicle maturation Gene SetFrom GO Biological Process Annotations 2015 genes participating in the hair follicle maturation biological process from the curated GO Biological Process Annotations 2015 dataset. |
Red vs non-red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Red vs non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Hair morphology Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Hair morphology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Black vs. red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Black vs. red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Blond vs. brown hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Blond vs. brown hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
Black vs. blond hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations genes associated with the Black vs. blond hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset. |
hair disease Gene SetFrom GWASdb SNP-Disease Associations genes associated with the disease hair disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset. |
abnormality of hair pigmentation Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset. |
red hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the red hair 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. |
abnormality of the hair Gene SetFrom GWASdb SNP-Phenotype Associations genes associated with the abnormality of the hair 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 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. |
patchy hypopigmentation of hair Gene SetFrom HPO Gene-Disease Associations genes associated with the patchy hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
brittle hair Gene SetFrom HPO Gene-Disease Associations genes associated with the brittle hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of secondary sexual hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of secondary sexual hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hypopigmentation of hair Gene SetFrom HPO Gene-Disease Associations genes associated with the hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
red hair Gene SetFrom HPO Gene-Disease Associations genes associated with the red hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
frontal upsweep of hair Gene SetFrom HPO Gene-Disease Associations genes associated with the frontal upsweep of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
fair hair Gene SetFrom HPO Gene-Disease Associations genes associated with the fair hair 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. |
absent facial hair Gene SetFrom HPO Gene-Disease Associations genes associated with the absent facial hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
projection of scalp hair onto lateral cheek Gene SetFrom HPO Gene-Disease Associations genes associated with the projection of scalp hair onto lateral cheek phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
premature graying of hair Gene SetFrom HPO Gene-Disease Associations genes associated with the premature graying of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the pubic hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the pubic hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
slow-growing hair Gene SetFrom HPO Gene-Disease Associations genes associated with the slow-growing hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent pubic hair Gene SetFrom HPO Gene-Disease Associations genes associated with the absent pubic hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
generalized hypopigmentation of hair Gene SetFrom HPO Gene-Disease Associations genes associated with the generalized hypopigmentation of hair 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. |
abnormality of hair growth rate Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of hair growth rate phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
curly hair Gene SetFrom HPO Gene-Disease Associations genes associated with the curly hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
melanin pigment aggregation in hair shafts Gene SetFrom HPO Gene-Disease Associations genes associated with the melanin pigment aggregation in hair shafts phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
coarse hair Gene SetFrom HPO Gene-Disease Associations genes associated with the coarse hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of hair texture Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of hair texture phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
scalp hair loss Gene SetFrom HPO Gene-Disease Associations genes associated with the scalp hair loss phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent axillary hair Gene SetFrom HPO Gene-Disease Associations genes associated with the absent axillary hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the scalp hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the scalp hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
thick hair Gene SetFrom HPO Gene-Disease Associations genes associated with the thick hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
woolly hair Gene SetFrom HPO Gene-Disease Associations genes associated with the woolly hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of hair pigmentation Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of hair pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
dry hair Gene SetFrom HPO Gene-Disease Associations genes associated with the dry hair 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. |
extension of hair growth on temples to lateral eyebrow Gene SetFrom HPO Gene-Disease Associations genes associated with the extension of hair growth on temples to lateral eyebrow phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
silver-gray hair Gene SetFrom HPO Gene-Disease Associations genes associated with the silver-gray hair 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 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. |
fine hair Gene SetFrom HPO Gene-Disease Associations genes associated with the fine hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
large clumps of pigment irregularly distributed along hair shaft Gene SetFrom HPO Gene-Disease Associations genes associated with the large clumps of pigment irregularly distributed along hair shaft phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hair-nail ectodermal dysplasia Gene SetFrom HPO Gene-Disease Associations genes associated with the hair-nail ectodermal dysplasia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of the axillary hair Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of the axillary hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
abnormality of hair density Gene SetFrom HPO Gene-Disease Associations genes associated with the abnormality of hair density phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
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. |
white hair Gene SetFrom HPO Gene-Disease Associations genes associated with the white hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes Gene SetFrom HPO Gene-Disease Associations genes associated with the hair shafts flattened at irregular intervals and twisted through 180 degrees about their axes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
absent hair Gene SetFrom HPO Gene-Disease Associations genes associated with the absent hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset. |
vestibular hair cell degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the vestibular hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
retarded hair growth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the retarded hair growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
whorled hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the whorled hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
long hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the long hair 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. |
absent cochlear hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent cochlear hair cell stereocilia 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 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. |
decreased cochlear hair cell stereocilia number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
brittle hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the brittle hair 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 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. |
cochlear inner hair cell degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent hair follicle pheomelanosome pheomelanin Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent hair follicle pheomelanosome pheomelanin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal auchene hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal auchene hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent hair follicle inner root sheath Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent hair follicle inner root sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cochlear hair cell degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cochlear hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cycle telogen phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cycle telogen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent cochlear hair bundle ankle links Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent cochlear hair bundle ankle links phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin vestibular hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent hair follicle melanin granules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent hair follicle melanin granules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair bundle inter-stereocilial links Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair bundle inter-stereocilial links phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin hair shaft Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin hair shaft phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal orientation of inner hair cell stereociliary bundles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal orientation of inner hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair-down neuron morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair-down neuron morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cuticle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cuticle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle dermal papilla morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle dermal papilla morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent hair follicle dermal papilla Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent hair follicle dermal papilla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent guard hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent guard hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner hair cell kinocilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased vestibular hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent vestibular hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cochlear hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated hair follicles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle infundibulum morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle infundibulum morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
underdeveloped hair follicles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the underdeveloped hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
distended hair follicles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the distended hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased zigzag hair amount Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased zigzag hair amount phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle outer root sheath morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle outer root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal outer hair cell kinocilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal outer hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cochlear outer hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased hair follicle apoptosis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased hair follicle apoptosis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hair follicle degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hair follicle degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal awl hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal awl hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased hair follicle number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased hair follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent cochlear outer hair cell electromotility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal orientation of outer hair cell stereociliary bundles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal orientation of outer hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent vestibular hair cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent vestibular hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent hair-down neurons Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent hair-down neurons phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent cochlear outer hair cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thick hair follicle outer rooth sheath Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thick hair follicle outer rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle melanin granule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair shaft melanin granule distribution Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair shaft melanin granule distribution phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair growth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair growth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle matrix region morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle matrix region morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner hair cell synaptic ribbon morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner hair cell synaptic ribbon morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
coarse hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the coarse hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent inner hair cell kinocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent inner hair cell kinocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair cell stereociliary bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal coat/hair pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal coat/hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal duvet hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal duvet hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cortex keratinization Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cortex keratinization phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent awl hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent awl hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle bulge morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle bulge morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair bundle ankle links morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair bundle ankle links morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle melanogenesis Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle melanogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear outer hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear outer hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
premature hair loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the premature hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair bundle tip links morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair bundle tip links morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair shaft melanin granule shape Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair shaft melanin granule shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cycle anagen phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cycle anagen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent cochlear inner hair cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent cochlear inner hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
fused outer hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the fused outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal inner hair cell stereociliary bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal inner hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
hair follicle outer rooth sheath hyperplasia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the hair follicle outer rooth sheath hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent hair follicles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair medulla Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair medulla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short cochlear hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear outer hair cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear outer hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair texture Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair texture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cochlear outer hair cell electromotility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin cochlear hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin cochlear hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
waved hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the waved hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear inner hair cell morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear inner hair cell morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cochlear inner hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear inner hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal coat/ hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal coat/ hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
focal dorsal hair loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
fused inner hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the fused inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased outer hair cell stereocilia number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased outer hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal guard hair morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal guard hair morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin hair follicle outer rooth sheath Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin hair follicle outer rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased inner hair cell stereocilia number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased inner hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair cell kinocilium morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell kinocilium morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent vestibular hair bundle shaft connectors Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent vestibular hair bundle shaft connectors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair cell inter-stereocilial links morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair cell inter-stereocilial links morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle orientation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle orientation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
thin hair follicle inner rooth sheath Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the thin hair follicle inner rooth sheath phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle melanin granule distribution Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle melanin granule distribution phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
ruffled hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the ruffled hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal tail hair pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal tail hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear outer hair cell electromotility Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear outer hair cell electromotility phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent outer hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short outer hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cell mechanoelectric transduction Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cell mechanoelectric transduction phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
focal hair loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the focal hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
reduced hair shaft melanin granule number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the reduced hair shaft melanin granule number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair bundle shaft connectors Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair bundle shaft connectors phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle pheomelanosome pheomelanin content Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle pheomelanosome pheomelanin content phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cycle Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cycle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent cochlear hair cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent cochlear hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair cell physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair cell physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle melanocyte morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle melanocyte morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair shaft melanin granule morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair shaft melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased guard hair length Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased guard hair length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal pinna hair pigmentation Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal pinna hair pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent active-zone-anchored inner hair cell synaptic ribbon Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent active-zone-anchored inner hair cell synaptic ribbon phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair medullary septa cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair medullary septa cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
progressive hair loss Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the progressive hair loss phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed hair regrowth Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed hair regrowth phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear outer hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
increased cochlear hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the increased cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged hair follicles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle physiology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
fused vestibular hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the fused vestibular hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cycle catagen phase Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cycle catagen phase phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
small hair follicles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the small hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal guard hair length Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal guard hair length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased cochlear outer hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased cochlear outer hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short cochlear outer hair cells Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
absent duvet hair Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the absent duvet hair phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair cell stereociliary bundle morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell stereociliary bundle morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle regression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle regression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
enlarged hair follicle melanin granules Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the enlarged hair follicle melanin granules phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair cortex morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair cortex morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased guard hair length Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased guard hair length phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair cell development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal vestibular hair cell development Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal vestibular hair cell development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal orientation of cochlear hair cell stereociliary bundles Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal orientation of cochlear hair cell stereociliary bundles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
cochlear outer hair cell degeneration Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the cochlear outer hair cell degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
short inner hair cell stereocilia Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated hair follicle infundibulum Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the dilated hair follicle infundibulum phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased vestibular hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased vestibular hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle inner root sheath morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle inner root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
decreased vestibular hair cell stereocilia number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the decreased vestibular hair cell stereocilia number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
distorted hair follicle pattern Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the distorted hair follicle pattern phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
accelerated hair follicle regression Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the accelerated hair follicle regression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
delayed hair appearance Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the delayed hair appearance phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair shedding Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair shedding phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal hair follicle bulb morphology Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal hair follicle bulb morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
abnormal cochlear hair cell number Gene SetFrom MPO Gene-Phenotype Associations gene mutations causing the abnormal cochlear hair cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset. |
dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis Gene SetFrom OMIM Gene-Disease Associations genes associated with the dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 3, blue/green eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 3, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
noonan-like syndrome with loose anagen hair Gene SetFrom OMIM Gene-Disease Associations genes associated with the noonan-like syndrome with loose anagen hair phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation, variation in, 8] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation, variation in, 8] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 3, light/dark/freckling skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 3, light/dark/freckling skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
woolly hair, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the woolly hair, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 6, hair/nail type Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 6, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 6, blue/green eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 6, blue/green eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 1, blue/nonblue eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 1, blue/nonblue eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
hair, curly Gene SetFrom OMIM Gene-Disease Associations genes associated with the hair, curly phenotype from the curated OMIM Gene-Disease Associations dataset. |
cardiomyopathy, dilated, with woolly hair and keratoderma Gene SetFrom OMIM Gene-Disease Associations genes associated with the cardiomyopathy, dilated, with woolly hair and keratoderma phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 7, hair/nail type Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 7, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 5, hair/nail type Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 5, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 4, hair/nail type Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 4, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset. |
palmoplantar keratoderma and woolly hair Gene SetFrom OMIM Gene-Disease Associations genes associated with the palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 11a, hypohidrotic/hair/tooth type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
woolly hair, autosomal recessive 1, with or without hypotrichosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the woolly hair, autosomal recessive 1, with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, dark/fair skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, dark/fair skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive phenotype from the curated OMIM Gene-Disease Associations dataset. |
obesity, adrenal insufficiency, and red hair due to pomc deficiency Gene SetFrom OMIM Gene-Disease Associations genes associated with the obesity, adrenal insufficiency, and red hair due to pomc deficiency phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 9, hair/nail type Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 9, hair/nail type phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 4, fair/dark skin] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 4, fair/dark skin] phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 8, hair/tooth/nail type Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 8, hair/tooth/nail type phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 5, dark/light eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 5, dark/light eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
woolly hair, autosomal recessive 2 with or without hypotrichosis Gene SetFrom OMIM Gene-Disease Associations genes associated with the woolly hair, autosomal recessive 2 with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset. |
[skin/hair/eye pigmentation 9, brown/nonbrown eyes] Gene SetFrom OMIM Gene-Disease Associations genes associated with the [skin/hair/eye pigmentation 9, brown/nonbrown eyes] phenotype from the curated OMIM Gene-Disease Associations dataset. |
arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair Gene SetFrom OMIM Gene-Disease Associations genes associated with the arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair phenotype from the curated OMIM Gene-Disease Associations dataset. |
cartilage-hair hypoplasia Gene SetFrom OMIM Gene-Disease Associations genes associated with the cartilage-hair hypoplasia phenotype from the curated OMIM Gene-Disease Associations dataset. |
ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant Gene SetFrom OMIM Gene-Disease Associations genes associated with the ectodermal dysplasia 10a, hypohidrotic/hair/nail type, autosomal dominant phenotype from the curated OMIM Gene-Disease Associations dataset. |
skin fragility-woolly hair syndrome Gene SetFrom OMIM Gene-Disease Associations genes associated with the skin fragility-woolly hair syndrome phenotype from the curated OMIM Gene-Disease Associations dataset. |
hair root Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue hair root from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
hair follicle Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue hair follicle from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
hair Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores proteins highly expressed in the tissue hair from the TISSUES Curated Tissue Protein Expression Evidence Scores dataset. |
hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
inner hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue inner hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair follicle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair follicle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair follicle outer root sheath Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair follicle outer root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair shaft Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair shaft in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair follicle inner root sheath Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair follicle inner root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair follicle bulge Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair follicle bulge in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair medulla Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair medulla in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
outer hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue outer hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair root Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair follicle bulge stem cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair follicle bulge stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
hair Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores proteins co-occuring with the tissue hair in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores dataset. |
Hair Follicle Development: Induction (Part 1 of 3)(Homo sapiens) Gene SetFrom WikiPathways Pathways 2014 proteins participating in the Hair Follicle Development: Induction (Part 1 of 3)(Homo sapiens) pathway from the WikiPathways Pathways 2014 dataset. |
Abnormal Hair Quantity Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Hair Quantity in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Cartilage-Hair Hypoplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Cartilage-Hair Hypoplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Generalized Hypopigmentation Of Hair Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Generalized Hypopigmentation Of Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Hair Texture Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Hair Texture in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Hair Density Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Hair Density in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormal Hair Pattern Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormal Hair Pattern in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Brittle Hair Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Brittle Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Menkes Kinky Hair Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Menkes Kinky Hair Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hair Shafts Flattened At Irregular Intervals And Twisted Through 180 Degrees About Their Axes Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hair Shafts Flattened At Irregular Intervals And Twisted Through 180 Degrees About Their Axes in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Skin/Hair/Eye Pigmentation Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Skin/Hair/Eye Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Hair Growth Rate Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Hair Growth Rate in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Skin Fragility-Woolly Hair Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Skin Fragility-Woolly Hair Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hair Follicle Nevus Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hair Follicle Nevus in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Abnormality Of Secondary Sexual Hair Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Abnormality Of Secondary Sexual Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Other Specified Nonscarring Hair Loss Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Other Specified Nonscarring Hair Loss in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Wooly Hair Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Wooly Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hair Follicle Neoplasm Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hair Follicle Neoplasm in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Wolly Hair Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Wolly Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Hair-Nail Ectodermal Dysplasia Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Hair-Nail Ectodermal Dysplasia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Loose Anagen Hair Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Loose Anagen Hair Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Amish Brittle Hair Brain Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Amish Brittle Hair Brain Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Uncombable Hair Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Uncombable Hair Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Congenital Abnormal Hair Pattern Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Congenital Abnormal Hair Pattern in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome Gene SetFrom DisGeNET Gene-Disease Associations genes associated with the disease Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset. |
Coarse Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Coarse Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hair Color Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hair Color in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Thick Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Thick Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fine Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fine Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Blonde Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Blonde Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Fair Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Fair Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Axillary Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Axillary Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Facial Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Facial Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Absent Pubic Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Absent Pubic Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Slow-Growing Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Slow-Growing Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Dry Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Dry Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Skin/Hair/Eye Pigmentation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Skin/Hair/Eye Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hypopigmentation Of Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hypopigmentation Of Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Wooly Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Wooly Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Curly Hair (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Curly Hair (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Patchy Hypopigmentation Of Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Patchy Hypopigmentation Of Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loss Of Scalp Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loss Of Scalp Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hair Whorls Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hair Whorls in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
White Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype White Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Silver-Gray Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Silver-Gray Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hair Morphology 1 Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hair Morphology 1 in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Hair Absent (Finding) Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Hair Absent (Finding) in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Extension Of Hair Growth On Temples To Lateral Eyebrow Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Extension Of Hair Growth On Temples To Lateral Eyebrow in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Brittle Scalp Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Brittle Scalp Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormality Of Hair Pigmentation Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormality Of Hair Pigmentation in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Red Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Red Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Hair Whorl Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Hair Whorl in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Abnormal Position Of Hair Whorl Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Abnormal Position Of Hair Whorl in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Large Clumps Of Pigment Irregularly Distributed Along Hair Shaft Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Large Clumps Of Pigment Irregularly Distributed Along Hair Shaft in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Melanin Pigment Aggregation In Hair Shafts Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Melanin Pigment Aggregation In Hair Shafts in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Uncombable Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Uncombable Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
Loose Anagen Hair Gene SetFrom DisGeNET Gene-Phenotype Associations genes associated with the phenotype Loose Anagen Hair in GWAS and other genetic association datasets from the DisGeNET Gene-Phenotype Associations dataset. |
regulation of hair cycle Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of hair cycle biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of hair cycle Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of hair cycle biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of hair follicle cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
hair cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the hair cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of hair follicle development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of hair follicle development biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of hair cycle by canonical Wnt signaling pathway Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of hair cycle by canonical Wnt signaling pathway biological process from the curated GO Biological Process Annotations 2023 dataset. |
hair follicle maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the hair follicle maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
hair follicle placode formation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the hair follicle placode formation biological process from the curated GO Biological Process Annotations 2023 dataset. |
neuromast hair cell development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the neuromast hair cell development biological process from the curated GO Biological Process Annotations 2023 dataset. |
posterior lateral line neuromast hair cell development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the posterior lateral line neuromast hair cell development biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of hair cycle Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of hair cycle biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of hair follicle development Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of hair follicle development biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of hair follicle cell proliferation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2023 dataset. |
negative regulation of hair follicle maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the negative regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
positive regulation of hair follicle maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the positive regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
regulation of hair follicle maturation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations 2023 dataset. |
neuromast hair cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the neuromast hair cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
posterior lateral line neuromast hair cell differentiation Gene SetFrom GO Biological Process Annotations 2023 genes participating in the posterior lateral line neuromast hair cell differentiation biological process from the curated GO Biological Process Annotations 2023 dataset. |
abnormal hair growth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair growth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear hair cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased vestibular hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased vestibular hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cochlear inner hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cochlear inner hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cochlear outer hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cochlear outer hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal coat/hair pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal coat/hair pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
vestibular hair cell degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the vestibular hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear outer hair cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear outer hair cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
retarded hair growth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the retarded hair growth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent duvet hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent duvet hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent cochlear hair cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cochlear hair cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cochlear inner hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cochlear inner hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cochlear outer hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cochlear outer hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle orientation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle orientation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
waved hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the waved hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair shaft morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair shaft morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair medulla Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair medulla phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal coat/ hair morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal coat/ hair morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair texture Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair texture phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal zigzag hair morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal zigzag hair morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased guard hair length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased guard hair length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cochlear hair cell degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cochlear inner hair cell degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear inner hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
cochlear outer hair cell degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the cochlear outer hair cell degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear hair cell stereociliary bundle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair cell stereociliary bundle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear hair cell development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair cell development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent hair follicles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent hair follicles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated hair follicle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated hair follicle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased hair follicle cell proliferation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased hair follicle cell proliferation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent cochlear inner hair cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cochlear inner hair cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent cochlear outer hair cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cochlear outer hair cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle melanocyte morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle melanocyte morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
accelerated hair follicle regression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the accelerated hair follicle regression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cycle catagen phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cycle catagen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
brittle hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the brittle hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased hair follicle number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased hair follicle number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small hair follicles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small hair follicles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent hair follicle melanin granules Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent hair follicle melanin granules phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
underdeveloped hair follicles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the underdeveloped hair follicles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
premature hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the premature hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cycle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cycle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent hair-down neurons Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent hair-down neurons phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal auchene hair morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal auchene hair morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal awl hair morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal awl hair morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
ruffled hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the ruffled hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed hair appearance Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed hair appearance phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
hair follicle outer root sheath hyperplasia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hair follicle outer root sheath hyperplasia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
distorted hair follicle pattern Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the distorted hair follicle pattern phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle inner root sheath morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle inner root sheath morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle dermal papilla morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle dermal papilla morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased hair follicle apoptosis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased hair follicle apoptosis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
small hair follicle bulb Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the small hair follicle bulb phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cortex keratinization Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cortex keratinization phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle melanogenesis Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle melanogenesis phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear outer hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear outer hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent outer hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent outer hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear inner hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear inner hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent vestibular hair cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent vestibular hair cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal orientation of cochlear hair cell stereociliary bundles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal orientation of cochlear hair cell stereociliary bundles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal outer hair cell stereociliary bundle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal outer hair cell stereociliary bundle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner hair cell stereociliary bundle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner hair cell stereociliary bundle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular hair cell kinocilium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular hair cell kinocilium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fused inner hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fused inner hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal guard hair morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal guard hair morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cuticle Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cuticle phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged hair follicles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged hair follicles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle melanin granule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle melanin granule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
hair follicle degeneration Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hair follicle degeneration phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle matrix region morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle matrix region morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner hair cell synaptic ribbon morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner hair cell synaptic ribbon morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent active-zone-anchored inner hair cell synaptic ribbon Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent active-zone-anchored inner hair cell synaptic ribbon phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair shaft melanin granule shape Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair shaft melanin granule shape phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular hair cell stereociliary bundle morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular hair cell stereociliary bundle morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased outer hair cell stereocilia number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased outer hair cell stereocilia number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal outer hair cell kinocilium location or orientation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal outer hair cell kinocilium location or orientation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair shaft melanin granule distribution Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair shaft melanin granule distribution phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased vestibular hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased vestibular hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased vestibular hair cell stereocilia number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased vestibular hair cell stereocilia number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased cochlear hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased cochlear hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal orientation of inner hair cell stereociliary bundles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal orientation of inner hair cell stereociliary bundles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cochlear outer hair cell electromotility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cochlear outer hair cell electromotility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short cochlear outer hair cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short cochlear outer hair cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear inner hair cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear inner hair cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular hair cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular hair cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent vestibular hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent vestibular hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
coarse hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the coarse hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased hair follicle number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased hair follicle number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short inner hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short inner hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
delayed hair regrowth Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the delayed hair regrowth phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cortex morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cortex morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cycle anagen phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cycle anagen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
reduced hair shaft melanin granule number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the reduced hair shaft melanin granule number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
progressive hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the progressive hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cell mechanoelectric transduction Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cell mechanoelectric transduction phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal orientation of outer hair cell stereociliary bundles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal orientation of outer hair cell stereociliary bundles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent cochlear outer hair cell electromotility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cochlear outer hair cell electromotility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fused outer hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fused outer hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short outer hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short outer hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle melanin granule distribution Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle melanin granule distribution phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent guard hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent guard hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in head/neck region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in head/neck region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dry hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dry hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal dorsal hair loss Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal dorsal hair loss phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased inner hair cell stereocilia number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased inner hair cell stereocilia number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent vestibular hair bundle shaft connectors Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent vestibular hair bundle shaft connectors phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin vestibular hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin vestibular hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin cochlear hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin cochlear hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin hair shaft Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin hair shaft phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cycle telogen phase Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cycle telogen phase phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
hair follicle comedo Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the hair follicle comedo phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
dilated hair follicle infundibulum Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the dilated hair follicle infundibulum phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle outer root sheath morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle outer root sheath morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent cochlear hair bundle ankle links Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cochlear hair bundle ankle links phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent hair follicle inner root sheath Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent hair follicle inner root sheath phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent awl hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent awl hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal pinna hair pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal pinna hair pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair medullary septa cells Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair medullary septa cells phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle peg morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle peg morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear hair cell physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair cell physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear hair cell inter-stereocilial links morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair cell inter-stereocilial links morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear hair bundle tip links morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair bundle tip links morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner hair cell kinocilium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner hair cell kinocilium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal outer hair cell kinocilium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal outer hair cell kinocilium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short cochlear hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short cochlear hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
fused vestibular hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the fused vestibular hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent cochlear hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent cochlear hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair cell morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair cell morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair shaft melanin granule morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair shaft melanin granule morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thick hair follicle outer root sheath Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thick hair follicle outer root sheath phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin hair follicle inner root sheath Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin hair follicle inner root sheath phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
long hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the long hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
increased guard hair length Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the increased guard hair length phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal inner hair cell kinocilium location or orientation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal inner hair cell kinocilium location or orientation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased zigzag hair amount Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased zigzag hair amount phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
enlarged hair follicle melanin granules Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the enlarged hair follicle melanin granules phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair shedding Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair shedding phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal vestibular hair cell development Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal vestibular hair cell development phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cochlear hair cell number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cochlear hair cell number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
decreased cochlear hair cell stereocilia number Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the decreased cochlear hair cell stereocilia number phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle regression Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle regression phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle pheomelanosome pheomelanin content Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle pheomelanosome pheomelanin content phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent hair follicle pheomelanosome pheomelanin Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent hair follicle pheomelanosome pheomelanin phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent inner hair cell kinocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent inner hair cell kinocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear outer hair cell electromotility Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear outer hair cell electromotility phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle bulb morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle bulb morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair medulla air spaces Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair medulla air spaces phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle infundibulum morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle infundibulum morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
thin hair follicle outer root sheath Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the thin hair follicle outer root sheath phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
short vestibular hair cell stereocilia Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the short vestibular hair cell stereocilia phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
distended hair follicles Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the distended hair follicles phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle ostium morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle ostium morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
whorled hair Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the whorled hair phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
absent hair follicle dermal papilla Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the absent hair follicle dermal papilla phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle physiology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle physiology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal tail hair pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal tail hair pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hair follicle bulge morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hair follicle bulge morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal hind foot hair pigmentation Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal hind foot hair pigmentation phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal cochlear hair bundle transient lateral links morphology Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the abnormal cochlear hair bundle transient lateral links morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in abdominal region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in abdominal region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
focal hair loss in thorax region Gene SetFrom MGI Mouse Phenotype Associations 2023 gene mutations causing the focal hair loss in thorax region phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset. |
abnormal coat/hair pigmentation Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal coat/hair pigmentation phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal coat/ hair morphology Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal coat/ hair morphology phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
abnormal hair growth Gene SetFrom IMPC Knockout Mouse Phenotypes gene knockouts causing the abnormal hair growth phenotype in mic from the IMPC Knockout Mouse Phenotypes dataset. |
Hair follicle cell_Amniotic fluid_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hair follicle cell_Amniotic fluid_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hair cell_Cochlea_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hair cell_Cochlea_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Inner hair cell_Cochlea_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Inner hair cell_Cochlea_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Outer hair cell_Cochlea_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Outer hair cell_Cochlea_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hair cell_Inner Ear_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hair cell_Inner Ear_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Outer hair cell_Inner Ear_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Outer hair cell_Inner Ear_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hair follicle cell_Hair follicle_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hair follicle cell_Hair follicle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hair follicle cell_Hair follicle_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hair follicle cell_Hair follicle_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Epithelial hair follicle stem cell_Hair follicle_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Epithelial hair follicle stem cell_Hair follicle_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hair follicle epithelial cell_Hair follicle_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hair follicle epithelial cell_Hair follicle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hair follicle cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hair follicle cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Vellus hair follicle cell_Skin_Human Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Vellus hair follicle cell_Skin_Human cell type from the CellMarker Gene-Cell Type Associations dataset. |
Stem cell_Upper hair follicle_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Stem cell_Upper hair follicle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Stem cell_Lower hair follicle_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Stem cell_Lower hair follicle_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hair canal cell_Hair canal_Mouse Gene SetFrom CellMarker Gene-Cell Type Associations genes associated with the Hair canal cell_Hair canal_Mouse cell type from the CellMarker Gene-Cell Type Associations dataset. |
Hair follicle development organogenesis part 2 of 3 Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Hair follicle development organogenesis part 2 of 3 pathway from the WikiPathways Pathways 2024 dataset. |
Hair follicle development cytodifferentiation stage 3 of 3 Gene SetFrom WikiPathways Pathways 2024 proteins participating in the Hair follicle development cytodifferentiation stage 3 of 3 pathway from the WikiPathways Pathways 2024 dataset. |
EDA signaling in hair follicle development Gene SetFrom WikiPathways Pathways 2024 proteins participating in the EDA signaling in hair follicle development pathway from the WikiPathways Pathways 2024 dataset. |
Acetylcholine inhibits contraction of outer hair cells Gene Setproteins participating in the Acetylcholine inhibits contraction of outer hair cells pathway from the Reactome Pathways 2024 dataset. |
Sensory processing of sound by inner hair cells of the cochlea Gene Setproteins participating in the Sensory processing of sound by inner hair cells of the cochlea pathway from the Reactome Pathways 2024 dataset. |
Sensory processing of sound by outer hair cells of the cochlea Gene Setproteins participating in the Sensory processing of sound by outer hair cells of the cochlea pathway from the Reactome Pathways 2024 dataset. |
regulation of hair cycle Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of hair cycle biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of hair cycle Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of hair cycle biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of hair follicle cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
hair cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the hair cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of hair follicle development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of hair follicle development biological process from the curated GO Biological Process Annotations 2025 dataset. |
hair follicle placode formation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the hair follicle placode formation biological process from the curated GO Biological Process Annotations 2025 dataset. |
hair follicle maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the hair follicle maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
neuromast hair cell development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the neuromast hair cell development biological process from the curated GO Biological Process Annotations 2025 dataset. |
posterior lateral line neuromast hair cell development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the posterior lateral line neuromast hair cell development biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of hair cycle Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of hair cycle biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of hair follicle development Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of hair follicle development biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of hair follicle cell proliferation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of hair follicle cell proliferation biological process from the curated GO Biological Process Annotations 2025 dataset. |
negative regulation of hair follicle maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the negative regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
positive regulation of hair follicle maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the positive regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
regulation of hair follicle maturation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the regulation of hair follicle maturation biological process from the curated GO Biological Process Annotations 2025 dataset. |
neuromast hair cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the neuromast hair cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
posterior lateral line neuromast hair cell differentiation Gene SetFrom GO Biological Process Annotations 2025 genes participating in the posterior lateral line neuromast hair cell differentiation biological process from the curated GO Biological Process Annotations 2025 dataset. |
Hair disease Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hair disease from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hair follicle neoplasm Gene SetFrom DISEASES Curated Gene-Disease Association Evidence Scores 2025 genes involed in the disease Hair follicle neoplasm from the DISEASES Curated Gene-Disease Association Evidence Scores 2025 dataset. |
Hair disease Gene SetFrom DISEASES Experimental Gene-Disease Association Evidence Scores 2025 genes associated with the disease Hair disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hair disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hair disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Familial woolly hair syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Familial woolly hair syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Noonan syndrome-like disorder with loose anagen hair 2 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome-like disorder with loose anagen hair 2 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hair follicle neoplasm Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Hair follicle neoplasm in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Pure hair and nail ectodermal dysplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Pure hair and nail ectodermal dysplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Loose anagen hair syndrome Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Loose anagen hair syndrome in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal dominant woolly hair Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal dominant woolly hair in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
cartilage-hair hypoplasia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease cartilage-hair hypoplasia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Noonan syndrome-like disorder with loose anagen hair Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome-like disorder with loose anagen hair in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Noonan syndrome-like disorder with loose anagen hair 1 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Noonan syndrome-like disorder with loose anagen hair 1 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Inflammatory poikiloderma with hair abnormalities and acral keratoses Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Inflammatory poikiloderma with hair abnormalities and acral keratoses in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Autosomal recessive woolly hair 3 Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores 2025 genes co-occuring with the disease Autosomal recessive woolly hair 3 in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset. |
Hair root Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Hair root from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Hair from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair follicle Gene SetFrom TISSUES Curated Tissue Protein Expression Evidence Scores 2025 proteins highly expressed in the tissue Hair follicle from the TISSUES Curated Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Outer hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Outer hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Inner hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Inner hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Cochlear hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Cochlear hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair follicle outer root sheath Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair follicle outer root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair follicle inner root sheath Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair follicle inner root sheath in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair follicle bulge Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair follicle bulge in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair follicle Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair follicle in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
hair-cell stereocilium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue hair-cell stereocilium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Vestibular hair cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Vestibular hair cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair follicle bulge stem cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair follicle bulge stem cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair shaft Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair shaft in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Plant glandular hair Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Plant glandular hair in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Plant hair Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Plant hair in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair medulla Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair medulla in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair follicle epithelium Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair follicle epithelium in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair root Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair root in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Hair follicle dermal papilla cell Gene SetFrom TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 proteins co-occuring with the tissue Hair follicle dermal papilla cell in abstracts of biomedical publications from the TISSUES Text-mining Tissue Protein Expression Evidence Scores 2025 dataset. |
Root hair Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Root hair cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Lateral wall of outer hair cell Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Lateral wall of outer hair cell cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Root hair tip Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Root hair tip cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Basal pole of outer hair cell Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Basal pole of outer hair cell cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cell hair Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cell hair cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
Cochlear hair cell ribbon synapse Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 proteins co-occuring with the Cochlear hair cell ribbon synapse cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset. |
SKIN/HAIR/EYE PIGMENTATION Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SKIN/HAIR/EYE PIGMENTATION phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Wooly hair Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Wooly hair phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Woolly hair Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Woolly hair phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hypopigmentation of hair Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hypopigmentation of hair phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Hair morphology Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Hair morphology phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Menkes kinky-hair syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Menkes kinky-hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Wooly hair nevus Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Wooly hair nevus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
SKIN/HAIR/EYE PIGMENTAT Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the SKIN/HAIR/EYE PIGMENTAT phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Woolly hair-skin fragility syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Woolly hair-skin fragility syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Skin fragility-woolly hair-palmoplantar keratoderma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Skin fragility-woolly hair-palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Uncombable hair syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Uncombable hair syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
TSPEAR-related disorder of tooth and hair follicle morphogenesis Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the TSPEAR-related disorder of tooth and hair follicle morphogenesis phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Skin and Hair Hypopigmentation Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Skin and Hair Hypopigmentation phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Curly hair Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Curly hair phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Wooly hair-palmoplantar keratoderma syndrome Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Wooly hair-palmoplantar keratoderma syndrome phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Premature graying of hair Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Premature graying of hair phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Autosomal dominant wooly hair Gene SetFrom ClinVar Gene-Phenotype Associations 2025 genes associated with the Autosomal dominant wooly hair phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset. |
Scalp hair shape Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Scalp hair shape phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hair greying Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hair greying phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blond vs non-blond hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blond vs non-blond hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Brown vs. non-brown hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Brown vs. non-brown hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Light vs. dark hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Light vs. dark hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red vs non-red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red vs non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Black vs. non-black hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Black vs. non-black hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Cutaneous melanoma or hair colour Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Cutaneous melanoma or hair colour phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Skin, hair and eye pigmentation (multivariate analysis) Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Skin, hair and eye pigmentation (multivariate analysis) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Straight vs curly hair Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Straight vs curly hair phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hair morphology traits Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hair morphology traits phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blond vs. brown hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blond vs. brown hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hair morphology Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hair morphology phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red vs. non-red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red vs. non-red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Black vs. blond hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Black vs. blond hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Black vs. red hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Black vs. red hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Hair shape Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Hair shape phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Red vs. brown/black hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Red vs. brown/black hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Blond vs. brown/black hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Blond vs. brown/black hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
Brown vs. black hair color Gene SetFrom GWAS Catalog SNP-Phenotype Associations 2025 genes associated with the Brown vs. black hair color phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations 2025 dataset. |
mammillary body, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in mammillary body, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
body of caudate nucleus, right Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in body of caudate nucleus, right relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
body of caudate nucleus, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in body of caudate nucleus, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
mammillary body, left Gene SetFrom Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles genes with high or low expression in mammillary body, left relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset. |
Nucleus of the trapezoid body Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Nucleus of the trapezoid body relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
Mammillary body Gene SetFrom Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles genes with high or low expression in Mammillary body relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset. |
body of caudate Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in body of caudate relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
pontobulbar body Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in pontobulbar body relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
pineal body Gene SetFrom Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles genes with high or low expression in pineal body relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset. |
Inclusion body myopathy 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, reducing body, X-linked, early-onset, severe Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, early-onset, severe phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Beta-thalassemia, dominant inclusion body type Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Beta-thalassemia, dominant inclusion body type phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease and frontotemporal dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease and frontotemporal dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Myopathy, reducing body, X-linked, childhood-onset Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Myopathy, reducing body, X-linked, childhood-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Polyglucosan body myopathy, early-onset, with or without immunodeficiency Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Polyglucosan body myopathy, early-onset, with or without immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
Lewy body dementia Gene SetFrom ClinVar Gene-Phenotype Associations genes associated with the Lewy body dementia phenotype from the curated ClinVar Gene-Phenotype Associations dataset. |
nuclear body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
flemming body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the flemming body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
nuclear inclusion body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the nuclear inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
lamellar body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cytoplasmic mrna processing body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cytoplasmic mrna processing body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
epidermal lamellar body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the epidermal lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
dense body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the dense body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cajal body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cajal body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
alveolar lamellar body membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the alveolar lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
lewy body core Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lewy body core cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
alveolar lamellar body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the alveolar lamellar body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cell body fiber Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cell body fiber cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
neuronal cell body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the neuronal cell body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
inclusion body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the inclusion body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
chromatoid body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the chromatoid body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
lamellar body membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lamellar body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cleavage body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cleavage body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
neuronal cell body membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the neuronal cell body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
xy body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the xy body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
multivesicular body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the multivesicular body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
histone locus body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the histone locus body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cell body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cell body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
ciliary basal body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the ciliary basal body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
weibel-palade body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the weibel-palade body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
pml body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the pml body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
multivesicular body membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the multivesicular body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
pip-body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the pip-body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
pi-body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the pi-body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
lewy body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the lewy body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
cell body membrane Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the cell body membrane cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
barr body Gene SetFrom COMPARTMENTS Curated Protein Localization Evidence Scores proteins localized to the barr body cellular component from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset. |
inclusion body Gene SetFrom COMPARTMENTS Experimental Protein Localization Evidence Scores proteins localized to the inclusion body cellular component in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset. |
er body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the er body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
spindle pole body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
nuclear body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
flemming body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the flemming body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
lewy body corona Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lewy body corona cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
nuclear inclusion body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
lamellar body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cytoplasmic mrna processing body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytoplasmic mrna processing body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
epidermal lamellar body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the epidermal lamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
pml body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the pml body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
dense body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the dense body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
smooth muscle dense body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the smooth muscle dense body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cortical lewy body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cortical lewy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cajal body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cajal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
osmiophilic body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the osmiophilic body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
dense nuclear body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the dense nuclear body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
new mitotic spindle pole body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the new mitotic spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
old mitotic spindle pole body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the old mitotic spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cell body fiber Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cell body fiber cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
mitotic spindle pole body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the mitotic spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
neuronal cell body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the neuronal cell body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
inclusion body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the inclusion body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
chromatoid body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the chromatoid body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
lamellar body membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lamellar body membrane 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. |
cleavage body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cleavage body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
meiotic spindle pole body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the meiotic spindle pole body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
bacterial-type flagellum basal body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the bacterial-type flagellum basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cell body membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cell body membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
lewy body core Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lewy body core cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
multivesicular body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the multivesicular body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
histone locus body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the histone locus body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cell body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cell body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
ciliary basal body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the ciliary basal body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
weibel-palade body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the weibel-palade body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
bunina body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the bunina body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
multivesicular body membrane Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the multivesicular body membrane cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
cytoplasmic u snrnp body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the cytoplasmic u snrnp body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
lewy body-like hyaline inclusion Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lewy body-like hyaline inclusion cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
pip-body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the pip-body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
ubisch body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the ubisch body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
pi-body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the pi-body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
protein body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the protein body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
lewy body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the lewy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
classical lewy body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the classical lewy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
barr body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the barr body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
yb body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the yb body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
laminated body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the laminated body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
complex laminated body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the complex laminated body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
pick body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the pick body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
nuclear dicing body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the nuclear dicing body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
apoptotic body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the apoptotic body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
etioplast prolamellar body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the etioplast prolamellar body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
xy body Gene SetFrom COMPARTMENTS Text-mining Protein Localization Evidence Scores proteins co-occuring with the xy body cellular component in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset. |
Heinz Body Anemias Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Heinz Body Anemias from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Reducing Body, X-Linked, Childhood-Onset Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Childhood-Onset from the curated CTD Gene-Disease Associations dataset. |
Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 9 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 8 from the curated CTD Gene-Disease Associations dataset. |
Granuloma, Foreign-Body Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Granuloma, Foreign-Body from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease 3, Autosomal Dominant Lewy Body Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 3, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Hyaline Body, Autosomal Recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Hyaline Body, Autosomal Recessive from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 11 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 13 from the curated CTD Gene-Disease Associations dataset. |
Body Weight Changes Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Body Weight Changes from the curated CTD Gene-Disease Associations dataset. |
MYOPATHY, SPHEROID BODY Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease MYOPATHY, SPHEROID BODY from the curated CTD Gene-Disease Associations dataset. |
Beta Thalassemia, Dominant Inclusion Body Type Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Beta Thalassemia, Dominant Inclusion Body Type from the curated CTD Gene-Disease Associations dataset. |
Lewy Body Disease Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Lewy Body Disease from the curated CTD Gene-Disease Associations dataset. |
Body Weight Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Body Weight from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 10 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 12 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 14 from the curated CTD Gene-Disease Associations dataset. |
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7 Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 7 from the curated CTD Gene-Disease Associations dataset. |
Inclusion Body Myopathy 3, Autosomal Dominant Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion Body Myopathy 3, Autosomal Dominant from the curated CTD Gene-Disease Associations dataset. |
Parkinson Disease 4, Autosomal Dominant Lewy Body Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Parkinson Disease 4, Autosomal Dominant Lewy Body from the curated CTD Gene-Disease Associations dataset. |
Inclusion body myopathy autosomal recessive Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Inclusion body myopathy autosomal recessive from the curated CTD Gene-Disease Associations dataset. |
Myositis, Inclusion Body Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myositis, Inclusion Body from the curated CTD Gene-Disease Associations dataset. |
Myopathy, Reducing Body, X-Linked, Early-Onset, Severe Gene SetFrom CTD Gene-Disease Associations genes/proteins associated with the disease Myopathy, Reducing Body, X-Linked, Early-Onset, Severe from the curated CTD Gene-Disease Associations dataset. |
Body Composition Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Composition in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Body Fat Distribution Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Fat Distribution in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Body Weights and Measures Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Weights and Measures in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Body Height Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Height in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Body Weight Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Weight in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Body Mass Index Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Mass Index in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
Body Weight Changes Gene SetFrom dbGAP Gene-Trait Associations genes associated with the trait Body Weight Changes in GWAS and other genetic association datasets from the dbGAP Gene-Trait Associations dataset. |
body dysmorphic disorder Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease body dysmorphic disorder in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
uterine body mixed cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease uterine body mixed cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
gastric body carcinoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease gastric body carcinoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
inclusion body myositis Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease inclusion body myositis in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ciliary body cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ciliary body cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
ciliary body disease Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease ciliary body disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
carotid body cancer Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease carotid body cancer in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
malignant ciliary body melanoma Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease malignant ciliary body melanoma in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
lewy body dementia Gene SetFrom DISEASES Text-mining Gene-Disease Association Evidence Scores genes co-occuring with the disease lewy body dementia in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset. |
higher body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease higher body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, type 1; obesity; pregnancy in diabetics in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
myositis, sporadic inclusion-body Gene SetFrom GAD Gene-Disease Associations genes associated with the disease myositis, sporadic inclusion-body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; insulin resistance; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucocorticoids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucocorticoids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; hypertension; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; coronary disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; coronary disease 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. |
body mass diabetes, type 2 glucose insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass diabetes, type 2 glucose insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; seasonal affective disorder Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; seasonal affective disorder in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol, ldl; cholesterol, total; insulin; apob Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, ldl; cholesterol, total; insulin; apob in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; left ventricular function; blood pressure; left ventricular structure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; left ventricular function; blood pressure; left ventricular structure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; insulin; glucose; hba(1c) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; insulin; glucose; hba(1c) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; leptin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; leptin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
larger body mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease larger body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; metabolic syndrome x Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; leukemia; breast cancer; glucose; cytogenetic studies; birth weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; glucose intolerance; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; glucose intolerance; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus, type 2; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus, type 2; obesity 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. |
body weights and measures Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weights and measures in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; thromboembolism Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; thromboembolism in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; hemoglobin a(1c) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; hemoglobin a(1c) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; weight gain Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; weight gain in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; left ventricular hypertrophy; glucose; blood pressure, arterial; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; glucose Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; glucose in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; hiv infections Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; hiv infections in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2 in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; puberty, delayed Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; puberty, delayed in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease birth weight; body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; triglycerides; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; triglycerides; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
gastric body ulcer Gene SetFrom GAD Gene-Disease Associations genes associated with the disease gastric body ulcer in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; hypertension; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; metabolic syndrome x in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sleep disorders; body mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sleep disorders; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; cardiovascular diseases; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; cardiovascular diseases; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; lipids; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; height; weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; height; weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
obesity; body weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease obesity; body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass index and waist circumference Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass index and waist circumference in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body burden of methylmercury Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body burden of methylmercury in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lower body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lower body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body composition changes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body composition changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; insulin resistance; obesity; syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; insulin resistance; obesity; syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; hypertension; glucose tolerance; insulin; blood pressure, arterial in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; hypertension; myocardial ischemia Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; hypertension; myocardial ischemia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; lipids; obesity; glucose; blood pressure; cortisol, salivary; leptin; leptin; testosterone in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body height Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dawson's inclusion body encephalitis; subacute sclerosing panencephalitis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dawson's inclusion body encephalitis; subacute sclerosing panencephalitis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
distal myopathies; myositis, inclusion body Gene SetFrom GAD Gene-Disease Associations genes associated with the disease distal myopathies; myositis, inclusion body in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
hyperhomocysteinemia; lewy body disease; psychomotor disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease hyperhomocysteinemia; lewy body disease; psychomotor disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes, gestational; gestational diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes, gestational; gestational diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
acromegaly; body weight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease acromegaly; body weight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
lewy body disease Gene SetFrom GAD Gene-Disease Associations genes associated with the disease lewy body disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
dietary intake and body composition Gene SetFrom GAD Gene-Disease Associations genes associated with the disease dietary intake and body composition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; lipids; blood pressure, arterial; heart rate; autonomic nervous system in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; gastrointestinal stromal tumors Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; gastrointestinal stromal tumors in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus; postoperative complications Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus; postoperative complications in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; familial mediterranean fever; recurrence Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; familial mediterranean fever; recurrence in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight changes Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight changes in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
glucose tolerance; insulin; body fat Gene SetFrom GAD Gene-Disease Associations genes associated with the disease glucose tolerance; insulin; body fat in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
sleep disorders; schizophrenia; body mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease sleep disorders; schizophrenia; body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; adiposity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; adiposity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; thinness Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; thinness in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; cystic fibrosis; growth disorders Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; cystic fibrosis; growth disorders in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body composition and muscle strength Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body composition and muscle strength in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body fat; insulin resistance Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body fat; insulin resistance in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass (lean) Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass (lean) in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; overweight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose tolerance; insulin; blood pressure; c-peptide; hba1c in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; crohn disease; crohn's disease; Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; crohn disease; crohn's disease; in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; obesity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; obesity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; insulin; glucose; nervous system activity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; insulin; glucose; nervous system activity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; muscle testing; igf-i Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; muscle testing; igf-i 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. |
body mass; diabetes, type 2; energy expenditure Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; diabetes, type 2; energy expenditure in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; hypertension; insulin sensitivity Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; hypertension; insulin sensitivity in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
plasma cholesterol levels and body mass index Gene SetFrom GAD Gene-Disease Associations genes associated with the disease plasma cholesterol levels and body mass index in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body composition Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body composition in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; hypertension; insulin; lipids Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; hypertension; insulin; lipids in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; diabetes mellitus type ii; diabetes mellitus, type 2; glucose intolerance; obesity; weight loss in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; polycystic ovary syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; polycystic ovary syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; birth weight; height Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; birth weight; height in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight; obesity; osteoarthritis, knee; overweight Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight; obesity; osteoarthritis, knee; overweight in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; bone density Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; bone density in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol; cholesterol, hdl; lipoprotein, ldl; triglycerides in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; glucose; insulin secretion Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; glucose; insulin secretion in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body weight regulation Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body weight regulation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; triglycerides; cholesterol, total; blood pressure; leptin; apoa1; apoa2; fasting blood sugar; fasting blood sugar in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
insulin; body fat; metabolic syndrome Gene SetFrom GAD Gene-Disease Associations genes associated with the disease insulin; body fat; metabolic syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass index in women. Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass index in women. in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; muscle testing Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; muscle testing in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |
body mass; cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl; hypertension; atherosclerosis Gene SetFrom GAD Gene-Disease Associations genes associated with the disease body mass; cholesterol, hdl; triglycerides; diabetes, type 2; cholesterol, ldl; hypertension; atherosclerosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset. |