abnormal hair medulla Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalies of hair medullary cell formation and arrangement of the innermost core of the hair shaft (Mammalian Phenotype Ontology, MP_0003812)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003812
Similar Terms
Downloads & Tools


11 gene mutations causing the abnormal hair medulla phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
C8ORF44-SGK3 C8orf44-SGK3 readthrough
EGFR epidermal growth factor receptor
FOXQ1 forkhead box Q1
KRT17 keratin 17, type I
KRT75 keratin 75, type II
LIPH lipase, member H
PKP3 plakophilin 3
PRSS8 protease, serine, 8
SOAT1 sterol O-acyltransferase 1
TGFA transforming growth factor, alpha
ZDHHC21 zinc finger, DHHC-type containing 21