rs2517381655
This variant is located in the CBS gene.
▶ClinVar annotation
HYPERHOMOCYSTEINEMIA, THROMBOTIC, CBS-RELATED
View on ClinVar →About CBS
The protein encoded by this gene acts as a homotetramer to catalyze the conversion of homocysteine to cystathionine, the first step in the transsulfuration pathway. The encoded protein is allosterically activated by adenosyl-methionine and uses pyridoxal phosphate as a cofactor. Defects in this gene can cause cystathionine beta-synthase deficiency (CBSD), which can lead to homocystinuria. This gene is a major contributor to cellular hydrogen sulfide production. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Feb 2016]
View all CBS variants →Gene information from NCBI Gene. Variant classifications from ClinVar.
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