decreased hair follicle number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description fewer number of the epidermal invaginations from which the hair shaft develops (Mammalian Phenotype Ontology, MP_0000379)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000379
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Genes

34 gene mutations causing the decreased hair follicle number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATR ATR serine/threonine kinase
B4GALT1 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1
BRCA1 breast cancer 1, early onset
CISD2 CDGSH iron sulfur domain 2
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
EDARADD EDAR-associated death domain
EGFR epidermal growth factor receptor
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
FIG4 FIG4 phosphoinositide 5-phosphatase
IGF1R insulin-like growth factor 1 receptor
IRF6 interferon regulatory factor 6
ITGB6 integrin, beta 6
KL klotho
KSR1 kinase suppressor of ras 1
LEF1 lymphoid enhancer-binding factor 1
LHX2 LIM homeobox 2
MPV17 MpV17 mitochondrial inner membrane protein
MPZL3 myelin protein zero-like 3
MTA2 metastasis associated 1 family, member 2
NCOA6 nuclear receptor coactivator 6
PDS5A PDS5 cohesin associated factor A
PNN pinin, desmosome associated protein
PRSS8 protease, serine, 8
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SFN stratifin
SLC27A4 solute carrier family 27 (fatty acid transporter), member 4
ST14 suppression of tumorigenicity 14 (colon carcinoma)
STAG1 stromal antigen 1
TAL1 T-cell acute lymphocytic leukemia 1
TP63 tumor protein p63
TRPS1 trichorhinophalangeal syndrome I
TWIST2 twist family bHLH transcription factor 2
ZDHHC13 zinc finger, DHHC-type containing 13