DISEASES

Disease-gene associations mined from literature

Literature associating SLC17A8 and autosomal dominant nonsyndromic deafness

SLC17A8 [ENSP00000316909]

Solute carrier family 17 (vesicular glutamate transporter), member 8; Mediates the uptake of glutamate into synaptic vesicles at presynaptic nerve terminals of excitatory neural cells. May also mediate the transport of inorganic phosphate; Deafness associated genes

Synonyms:  SLC17A8,  SLC17A8p,  hSLC17A8,  Q8NDX2,  Q8NDX2p ...

Linkouts:  STRING  Pharos  UniProt  OMIM