abnormality of dermal melanosomes Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the melanosomes, i.e., of the cellular organelles in which melanin pigments are synthesized and stored within melanocytes (the cells that produce pigment in the dermis). (Human Phenotype Ontology, HP_0011125)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011125
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Genes

7 genes associated with the abnormality of dermal melanosomes 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
GPR143 G protein-coupled receptor 143
LYST lysosomal trafficking regulator
MITF microphthalmia-associated transcription factor
MYO5A myosin VA (heavy chain 12, myoxin)
RAB27A RAB27A, member RAS oncogene family
TYR tyrosinase