Gene Gene information from NCBI Gene database.
Entrez ID 114789
Gene name Solute carrier family 25 member 25
Gene symbol SLC25A25
Synonyms (NCBI Gene)
MCSCPCSCLSCAMC-2SCAMC2
Chromosome 9
Chromosome location 9q34.11
Summary The protein encoded by this gene belongs to the family of calcium-binding mitochondrial carriers, with a characteristic mitochondrial carrier domain at the C-terminus. These proteins are found in the inner membranes of mitochondria, and function as transp
miRNA miRNA information provided by mirtarbase database.
338
miRTarBase ID miRNA Experiments Reference
MIRT666303 hsa-miR-501-5p HITS-CLIP 23824327
MIRT666302 hsa-miR-4457 HITS-CLIP 23824327
MIRT666301 hsa-miR-877-3p HITS-CLIP 23824327
MIRT666300 hsa-miR-205-5p HITS-CLIP 23824327
MIRT666299 hsa-miR-1236-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
23
GO ID Ontology Definition Evidence Reference
GO:0002021 Process Response to dietary excess IEA
GO:0005347 Function ATP transmembrane transporter activity IBA
GO:0005509 Function Calcium ion binding IEA
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IDA 15054102, 15123600
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608745 20663 ENSG00000148339
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6KCM7
Protein name Mitochondrial adenyl nucleotide antiporter SLC25A25 (Mitochondrial ATP-Mg/Pi carrier protein 3) (Mitochondrial Ca(2+)-dependent solute carrier protein 3) (Short calcium-binding mitochondrial carrier protein 2) (SCaMC-2) (Solute carrier family 25 member 25
Protein function Electroneutral antiporter that most probably mediates the transport of adenyl nucleotides through the inner mitochondrial membrane. Originally identified as an ATP-magnesium/inorganic phosphate antiporter, it could have a broader specificity for
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13833 EF-hand_8 52 79 EF-hand domain pair Domain
PF13499 EF-hand_7 80 142 EF-hand domain pair Domain
PF00153 Mito_carr 182 275 Mitochondrial carrier protein Family
PF00153 Mito_carr 276 368 Mitochondrial carrier protein Family
PF00153 Mito_carr 373 467 Mitochondrial carrier protein Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed. Expressed in fetal and adult liver, skeletal muscle, testis, ovary, hippocampus and caudate nucleus. {ECO:0000269|PubMed:15054102, ECO:0000269|PubMed:15123600}.; TISSUE SPECIFICITY: [Isoform 1]: Expressed in all tissu
Sequence
Sequence length 469
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Nephrolithiasis Pathogenic rs140777921 RCV001280533
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
AUTISM SPECTRUM DISORDER CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
AUTISM SPECTRUM DISORDERS Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
High myopia Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SEVERE MYOPIA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Asthma Associate 31300640
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Inhibit 27553025
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 1 Associate 33083497
★☆☆☆☆
Found in Text Mining only
Kidney Calculi Associate 34346195
★☆☆☆☆
Found in Text Mining only
Neoplasms Inhibit 27553025
★☆☆☆☆
Found in Text Mining only