abnormality of hair pigmentation Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of hair pigmentation (color). (Human Phenotype Ontology, HP_0009887)
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0009887
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Genes

29 genes associated with the abnormality of hair pigmentation phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
HERC2 HECT and RLD domain containing E3 ubiquitin protein ligase 2 3.24415
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor) 3.19268
FANCA Fanconi anemia, complementation group A 2.92274
CDK10 cyclin-dependent kinase 10 2.75062
OCA2 oculocutaneous albinism II 2.6129
AFG3L1P AFG3-like AAA ATPase 1, pseudogene 2.60742
ZNF276 zinc finger protein 276 2.37936
DPEP1 dipeptidase 1 (renal) 2.36934
SPATA33 spermatogenesis associated 33 2.3534
SPIRE2 spire-type actin nucleation factor 2 2.22908
TPCN2 two pore segment channel 2 2.2238
IRF4 interferon regulatory factor 4 2.19981
CHMP1A charged multivesicular body protein 1A 2.0492
PRDM7 PR domain containing 7 1.96614
DBNDD1 dysbindin (dystrobrevin binding protein 1) domain containing 1 1.93111
ANKRD11 ankyrin repeat domain 11 1.84749
CDK5RAP1 CDK5 regulatory subunit associated protein 1 1.74205
SPATA2L spermatogenesis associated 2-like 1.6456
CPNE7 copine VII 1.62822
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive) 1.58889
TUBB3 tubulin, beta 3 class III 1.51389
DEF8 differentially expressed in FDCP 8 homolog (mouse) 1.47003
GAS8 growth arrest-specific 8 1.37522
SLC45A2 solute carrier family 45, member 2 1.30523
SLC24A4 solute carrier family 24 (sodium/potassium/calcium exchanger), member 4 1.2976
ZNF778 zinc finger protein 778 1.28922
CENPBD1 CENPB DNA-binding domains containing 1 1.2335
EXOC2 exocyst complex component 2 1.17192
KIRREL3 kin of IRRE like 3 (Drosophila) 1.09906