1186
26373
ENSG00000103249
ENSMUSG00000036636
P51798
O70496
NM_001114331NM_001287
NM_011930NM_001317404
NP_001107803NP_001278
NP_001304333NP_036060
Chloride channel 7 alpha subunit also known as H+/Cl− exchange transporter 7 is a protein that in humans is encoded by the CLCN7 gene.[5] In melanocytic cells this gene is regulated by the Microphthalmia-associated transcription factor.[6][7]
Mutations in the CLCN7 gene have been reported to be associated with autosomal dominant osteopetrosis type II, a rare disease of bones.[8]
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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