white forelock Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A triangular depigmented region of white hairs located in the anterior midline of the scalp. (Human Phenotype Ontology, HP_0002211)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002211
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Genes

10 genes associated with the white forelock phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
EDN3 endothelin 3
EDNRB endothelin receptor type B
KIT v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog
MITF microphthalmia-associated transcription factor
PAX3 paired box 3
PEPD peptidase D
SNAI2 snail family zinc finger 2
SOX10 SRY (sex determining region Y)-box 10
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
WRN Werner syndrome, RecQ helicase-like