mottled pigmentation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Patchy and irregular skin pigmentation. (Human Phenotype Ontology, HP_0001070)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001070
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Genes

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

Symbol Name
KRT5 keratin 5, type II
LMNA lamin A/C
RECQL4 RecQ protein-like 4
ZMPSTE24 zinc metallopeptidase STE24