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Gene entry

SLC25A15

solute carrier family 25 member 15

Chromosome
13
Cytoband
13q14.11
Variants (rsID)
11

SLC25A15 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 13 (region 13q14.11). Its official name is “solute carrier family 25 member 15”. The reference table lists 11 variants (rsID) for this gene.

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Clinically classified variants

4 reference-table entries with clinical significance.

  • rs112276566Benignsingle nucleotide variantHyperornithinemia-hyperammonemia-homocitrullinuria syndrome
  • rs9577152Benignsingle nucleotide variantHyperornithinemia-hyperammonemia-homocitrullinuria syndrome
  • rs104894424Pathogenicsingle nucleotide variantHyperornithinemia-hyperammonemia-homocitrullinuria syndrome
  • rs104894430Pathogenicsingle nucleotide variantHyperornithinemia-hyperammonemia-homocitrullinuria syndrome

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.