rs2505740381
This variant is located in the STRA6 gene.
▶ClinVar annotation
About STRA6
The protein encoded by this gene is a membrane protein involved in the metabolism of retinol. The encoded protein acts as a receptor for retinol/retinol binding protein complexes. This protein removes the retinol from the complex and transports it across the cell membrane. Defects in this gene are a cause of syndromic microphthalmia type 9 (MCOPS9). Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
View all STRA6 variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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