Home > Gene Browser > SLC25A52

SLC25A52

Synonyms
MCART2
External resources
Summary
This gene is similar to the mitochondrial carrier triple repeat 1 gene on chromosome 9. The gene is intronless and may be an evolving pseudogene; however, it is transcribed and it contains a full-length coding region so it is currently classified as a protein-coding locus.

Variant counts

The variants found in rare patients tested by 3billion are classified and counted according to ACMG guidelines. The variants with over 5% variant frequency in population genome databases ( gnomAD, dbSNP, etc) are excluded.

Pathogenic
0
Likely pathogenic
0
VUS
550
Likely benign
15
Benign
0

Patient phenotypes

No patients carry pathogenic or likely pathogenic variants on SLC25A52 gene.

Phenotype class
Patients in 3billion (%)

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