underdeveloped hair follicles Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description arrest of or retarded differentiation of the epidermal invaginations from which the hair shaft develops (Mammalian Phenotype Ontology, MP_0000382)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000382
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16 gene mutations causing the underdeveloped hair follicles phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AKT1 v-akt murine thymoma viral oncogene homolog 1
CTSV cathepsin V
EDARADD EDAR-associated death domain
FOXN1 forkhead box N1
ITPA inosine triphosphatase (nucleoside triphosphate pyrophosphatase)
LEF1 lymphoid enhancer-binding factor 1
LHX2 LIM homeobox 2
MPZL3 myelin protein zero-like 3
PKP3 plakophilin 3
PPARD peroxisome proliferator-activated receptor delta
PRSS8 protease, serine, 8
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RUNX2 runt-related transcription factor 2
RYR1 ryanodine receptor 1 (skeletal)
SAV1 salvador family WW domain containing protein 1
ZDHHC21 zinc finger, DHHC-type containing 21