irregular coat pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description uneven coloration of the hair (Mammalian Phenotype Ontology, MP_0000372)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000372
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Genes

21 gene mutations causing the irregular 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
BCL2 B-cell CLL/lymphoma 2
EDA ectodysplasin A
FREM2 FRAS1 related extracellular matrix protein 2
HTR2C 5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KITLG KIT ligand
MCOLN3 mucolipin 3
MITF microphthalmia-associated transcription factor
MYSM1 Myb-like, SWIRM and MPN domains 1
NSDHL NAD(P) dependent steroid dehydrogenase-like
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
OCA2 oculocutaneous albinism II
PEPD peptidase D
PMEL premelanosome protein
RPL38 ribosomal protein L38
SLC45A2 solute carrier family 45, member 2
TBX15 T-box 15
TRAPPC6A trafficking protein particle complex 6A
TYR tyrosinase