absent skin pigmentation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of skin pigmentation (coloring). (Human Phenotype Ontology, HP_0200098)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0200098
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Genes

3 genes associated with the absent skin pigmentation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
SNAI2 snail family zinc finger 2
TYR tyrosinase