abnormal hair follicle bulge morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the area located in the bottom of the permanent portion of a resting (telogen) hair follicle where the cells of the external root sheath of the hair follicle are contiguous with the basal layer of the epidermis; this portion of the follicle is involved in the generation of a new hair at the onset of the hair growth cycle (anagen) and contains the hair follicle stem cells (Mammalian Phenotype Ontology, MP_0009759)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009759
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10 gene mutations causing the abnormal hair follicle bulge morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARPC2 actin related protein 2/3 complex, subunit 2, 34kDa
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
SLC16A2 solute carrier family 16, member 2 (thyroid hormone transporter)
TMEM98 transmembrane protein 98
TRAF3IP3 TRAF3 interacting protein 3