hair follicle outer rooth sheath hyperplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description overdevelopment or increased size, usually due to a increased number of cells, 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_0010688)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010688
Similar Terms
Downloads & Tools

Genes

4 gene mutations causing the hair follicle outer rooth sheath hyperplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AARS alanyl-tRNA synthetase
BMP7 bone morphogenetic protein 7
CTSV cathepsin V
DSG4 desmoglein 4