Gene entry

SLC25A42

solute carrier family 25 member 42

Chromosome: 19
Cytoband: 19p13.11
Variants (rsID): 2

SLC25A42 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 19 (region 19p13.11). Its official name is “solute carrier family 25 member 42”. The reference table lists 2 variants (rsID) for this gene.

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Clinically classified variants

1 reference-table entries with clinical significance.

rs864321624Pathogenicsingle nucleotide variantInborn mitochondrial myopathy|Metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression|SLC25A42-related mitochondrial disorder

Other listed variants

rs77795295

Public references

NCBI Gene
Ensembl
ClinVar

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.