generalized hypopigmentation of hair Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Reduced pigmentation of hair diffusely. (Human Phenotype Ontology, HP_0011358)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0011358
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Genes

17 genes associated with the generalized hypopigmentation of hair phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
AP3B1	adaptor-related protein complex 3, beta 1 subunit
CDKL5	cyclin-dependent kinase-like 5
ESCO2	establishment of sister chromatid cohesion N-acetyltransferase 2
LPAR6	lysophosphatidic acid receptor 6
MECP2	methyl CpG binding protein 2
MLPH	melanophilin
MYO5A	myosin VA (heavy chain 12, myoxin)
PAH	phenylalanine hydroxylase
PDE4D	phosphodiesterase 4D, cAMP-specific
RAB27A	RAB27A, member RAS oncogene family
RMRP	RNA component of mitochondrial RNA processing endoribonuclease
SLC17A5	solute carrier family 17 (acidic sugar transporter), member 5
TP63	tumor protein p63
TYR	tyrosinase
UBE3A	ubiquitin protein ligase E3A
UBR1	ubiquitin protein ligase E3 component n-recognin 1
UROC1	urocanate hydratase 1