abnormal hair shaft melanin granule morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of pigment polymers in the hair shaft (Mammalian Phenotype Ontology, MP_0008731)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008731
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10 gene mutations causing the abnormal hair shaft melanin granule morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARCN1 archain 1
ATP7A ATPase, Cu++ transporting, alpha polypeptide
FOXN1 forkhead box N1
GATA3 GATA binding protein 3
LIPH lipase, member H
LYST lysosomal trafficking regulator
MITF microphthalmia-associated transcription factor
PMEL premelanosome protein
SLC24A5 solute carrier family 24 (sodium/potassium/calcium exchanger), member 5
ZDHHC21 zinc finger, DHHC-type containing 21