abnormal otic pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the pigment or pigment-producing cells of the inner ear resulting in abnormal melanoblast numbers, distribution, or pigment during development (Mammalian Phenotype Ontology, MP_0009390)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009390
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8 gene mutations causing the abnormal otic pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EDNRB endothelin receptor type B
FAS Fas cell surface death receptor
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MITF microphthalmia-associated transcription factor
NDP Norrie disease (pseudoglioma)
S1PR2 sphingosine-1-phosphate receptor 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4
TYRP1 tyrosinase-related protein 1