Gene entry
ST3GAL5
ST3 beta-galactoside alpha-2,3-sialyltransferase 5
- Chromosome
- 2
- Cytoband
- 2p11.2
- Variants (rsID)
- 9
ST3GAL5 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p11.2). Its official name is “ST3 beta-galactoside alpha-2,3-sialyltransferase 5”. The reference table lists 9 variants (rsID) for this gene.
Clinically classified variants
5 reference-table entries with clinical significance.
- rs1138484Benignsingle nucleotide variantGM3 synthase deficiency
- rs149309844Benignsingle nucleotide variantGM3 synthase deficiency
- rs148195895Conflicting interpretationssingle nucleotide variantGM3 synthase deficiency
- rs149801673Conflicting interpretationssingle nucleotide variantGM3 synthase deficiency
- rs199590656Conflicting interpretationssingle nucleotide variantGM3 synthase deficiency
Other listed variants
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.
