premature graying of hair Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Development of gray hair at a younger than normal age. (Human Phenotype Ontology, HP_0002216)
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23 genes associated with the premature graying of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ATM ATM serine/threonine kinase
CTC1 CTS telomere maintenance complex component 1
DKC1 dyskeratosis congenita 1, dyskerin
EDN3 endothelin 3
EDNRB endothelin receptor type B
MITF microphthalmia-associated transcription factor
MTAP methylthioadenosine phosphorylase
MYO5A myosin VA (heavy chain 12, myoxin)
NHP2 NHP2 ribonucleoprotein
NOP10 NOP10 ribonucleoprotein
PAX3 paired box 3
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
RAB27A RAB27A, member RAS oncogene family
RECQL4 RecQ protein-like 4
RTEL1 regulator of telomere elongation helicase 1
SNAI2 snail family zinc finger 2
SOX10 SRY (sex determining region Y)-box 10
TERC telomerase RNA component
TERT telomerase reverse transcriptase
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
USB1 U6 snRNA biogenesis 1
WRAP53 WD repeat containing, antisense to TP53