rs576315457

This variant is located in the CTNS gene.

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ClinVar annotation

Conflicting Classifications
3 submitters2 publications

Inborn genetic diseases;Ocular cystinosis;Juvenile nephropathic cystinosis; Inborn genetic diseases; Nephropathic cystinosis;Ocular cystinosis;Juvenile nephropathic cystinosis

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About CTNS

This gene encodes a seven-transmembrane domain protein that functions to transport cystine out of lysosomes. Its activity is driven by the H+ electrochemical gradient of the lysosomal membrane. Mutations in this gene cause cystinosis, a lysosomal storage disorder. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2009]

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Gene information from NCBI Gene. Variant classifications from ClinVar.

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