abnormal hair texture Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description irregular or unusual appearance of the structure of the hair (Mammalian Phenotype Ontology, MP_0002074)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002074
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47 gene mutations causing the abnormal hair texture phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACD adrenocortical dysplasia homolog (mouse)
AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2
ARPC4 actin related protein 2/3 complex, subunit 4, 20kDa
ATP7A ATPase, Cu++ transporting, alpha polypeptide
C8ORF44-SGK3 C8orf44-SGK3 readthrough
COL1A1 collagen, type I, alpha 1
CTSV cathepsin V
DSG4 desmoglein 4
EDA ectodysplasin A
EDAR ectodysplasin A receptor
EDARADD EDAR-associated death domain
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
EGFR epidermal growth factor receptor
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
ERCC2 excision repair cross-complementation group 2
FBLN5 fibulin 5
FGF7 fibroblast growth factor 7
FOXN1 forkhead box N1
FOXQ1 forkhead box Q1
GATA3 GATA binding protein 3
GOLM1 golgi membrane protein 1
HOXC13 homeobox C13
IL2RB interleukin 2 receptor, beta
INHBA inhibin, beta A
KMT2A lysine (K)-specific methyltransferase 2A
KRT17 keratin 17, type I
KRT25 keratin 25, type I
KRT71 keratin 71, type II
KRT75 keratin 75, type II
KRT76 keratin 76, type II
LIPH lipase, member H
LMNA lamin A/C
MPZL3 myelin protein zero-like 3
NCOA3 nuclear receptor coactivator 3
NFKB1 nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
PKP3 plakophilin 3
PRLR prolactin receptor
PRSS8 protease, serine, 8
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SGSH N-sulfoglucosamine sulfohydrolase
SQSTM1 sequestosome 1
TGFA transforming growth factor, alpha
TGM3 transglutaminase 3
TMEM79 transmembrane protein 79
VEGFA vascular endothelial growth factor A
ZDHHC13 zinc finger, DHHC-type containing 13
ZDHHC21 zinc finger, DHHC-type containing 21