absent coat pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description fur or hair is devoid of coloration and appears white (Mammalian Phenotype Ontology, MP_0005171)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005171
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10 gene mutations causing the absent coat pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASIP agouti signaling protein
ATP7A ATPase, Cu++ transporting, alpha polypeptide
EDNRB endothelin receptor type B
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KITLG KIT ligand
MITF microphthalmia-associated transcription factor
PAX3 paired box 3
RECQL4 RecQ protein-like 4
SOX10 SRY (sex determining region Y)-box 10
TYR tyrosinase