abnormal pinna hair pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description amount and distribution of yellow pigment (phaeomelanin) relative to black or brown pigment (eumelanin) is decreased or increased in hair located behind the ears when compared to control animal pigmentation (Mammalian Phenotype Ontology, MP_0009928)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009928
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3 gene mutations causing the abnormal pinna hair pigmentation 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)
SLC45A2 solute carrier family 45, member 2