57709241919ENSG00000013293ENSMUSG00000069072Q8TBB6Q8BXR1NM_020949NM_175917NM_172861NP_066000NP_766449Solute carrier family 7, member 14 is a protein that in humans is encoded by the SLC7A14 gene.

[5] This gene is predicted to encode a glycosylated, cationic amino acid transporter protein with 14 transmembrane domains.

In the mammalian inner ear, this gene is expressed in neonatal inner and outer hair cells during development and becomes specifically expressed in inner hair cells in adult animals,.

[6][7]Mutations in this gene are associated with autosomal recessive retinitis pigmentosa and hearing loss in the form of auditory neuropathy.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.