ATP6V1H (ATPase H+ Transporting V1 Subunit H) is a Protein Coding gene. Diseases associated with ATP6V1H include Cutis Laxa, Autosomal Recessive, Type Iid and Sorsby Fundus Dystrophy. Among its related pathways are Nef-mediates down modulation of cell surface receptors by recruiting them to clathrin adapters and HIV Life Cycle. Gene Ontology (GO) annotations related to this gene include binding and proton-transporting ATPase activity, rotational mechanism.
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