abnormal hair follicle outer root sheath morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the outermost layer of the hair follicle that merges proximally with the basal layer of the interfollicular epidermis and distally with the hair bulb (Mammalian Phenotype Ontology, MP_0010684)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010684
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Genes

17 gene mutations causing the abnormal hair follicle outer root sheath morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AARS alanyl-tRNA synthetase
ARPC2 actin related protein 2/3 complex, subunit 2, 34kDa
BMP7 bone morphogenetic protein 7
C8ORF44-SGK3 C8orf44-SGK3 readthrough
CTSV cathepsin V
DSG4 desmoglein 4
HERC3 HECT and RLD domain containing E3 ubiquitin protein ligase 3
KDM7A lysine (K)-specific demethylase 7A
MYO6 myosin VI
OXR1 oxidation resistance 1
PEX3 peroxisomal biogenesis factor 3
RHOT2 ras homolog family member T2
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
TMEM98 transmembrane protein 98
TMPRSS6 transmembrane protease, serine 6
TRAF3IP3 TRAF3 interacting protein 3