absent skin pigmentation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Lack of skin pigmentation (coloring). (Human Phenotype Ontology, HP_0200098)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001189
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Genes

7 gene mutations causing the absent skin pigmentation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
KITLG KIT ligand
MITF microphthalmia-associated transcription factor
PAX3 paired box 3
PTPN6 protein tyrosine phosphatase, non-receptor type 6
SPAG9 sperm associated antigen 9
TYR tyrosinase