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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.