The SLC25A4 gene homepage

General information
Gene symbol SLC25A4
Gene name solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4
Chromosome 4
Chromosomal band q35
Imprinted Unknown
Genomic reference NG_013001.1
Transcript reference NM_001151.3
Exon/intron information NM_001151.3 exon/intron table
Associated with diseases MTDPS12, MTDPS12A, PEOA2
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 10
Unique public DNA variants reported 9
Individuals with public variants 3
Hidden variants -
Date created November 14, 2012
Date last updated November 01, 2022
Version SLC25A4:221101

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_001151.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
HGNC 10990
Entrez Gene 291
PubMed articles SLC25A4
OMIM - Gene 103220
OMIM - Diseases MTDPS12 (mitochondrial DNA depletion syndrome, type 12 (MTDPS-12, cardiomyopathic type))
MTDPS12A (Mi DNA depletion syndrome 12A (cardiomyopathic type) AD)
PEOA2 (ophthalmoplegia, external, progressive, with mitochondrial DNA deletions, autosomal dominant, type 2 (PEOA-2))
GeneCards SLC25A4
GeneTests SLC25A4
Orphanet SLC25A4

Active transcripts




NCBI ID     

NCBI Protein ID     

00001757 4 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4 NM_001151.3 NP_001142.2 10

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