abnormal hair follicle melanogenesis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure of or anomaly in the biosynthetic pathway of melanin formation in hair follicles (Mammalian Phenotype Ontology, MP_0004382)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004382
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Genes

4 gene mutations causing the abnormal hair follicle melanogenesis phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASIP agouti signaling protein
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
RAB38 RAB38, member RAS oncogene family
TYR tyrosinase