Gene Gene information from NCBI Gene database.
Entrez ID 292
Gene name Solute carrier family 25 member 5
Gene symbol SLC25A5
Synonyms (NCBI Gene)
2F1AAC2ANT2T2T3
Chromosome X
Chromosome location Xq24
Summary This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix i
miRNA miRNA information provided by mirtarbase database.
259
miRTarBase ID miRNA Experiments Reference
MIRT050085 hsa-miR-26a-5p CLASH 23622248
MIRT047644 hsa-miR-10a-5p CLASH 23622248
MIRT047467 hsa-miR-10b-5p CLASH 23622248
MIRT046196 hsa-miR-27b-3p CLASH 23622248
MIRT044296 hsa-miR-106b-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
49
GO ID Ontology Definition Evidence Reference
GO:0000295 Function Adenine nucleotide transmembrane transporter activity IMP 19116139
GO:0003723 Function RNA binding HDA 22658674
GO:0005471 Function ATP:ADP antiporter activity IEA
GO:0005471 Function ATP:ADP antiporter activity ISS
GO:0005515 Function Protein binding IPI 17715127, 19116139, 19130895, 19154410, 21370995, 24725412, 27499296, 31883789
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300150 10991 ENSG00000005022
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P05141
Protein name ADP/ATP translocase 2 (ADP,ATP carrier protein 2) (ADP,ATP carrier protein, fibroblast isoform) (Adenine nucleotide translocator 2) (ANT 2) (Solute carrier family 25 member 5) [Cleaved into: ADP/ATP translocase 2, N-terminally processed]
Protein function ADP:ATP antiporter that mediates import of ADP into the mitochondrial matrix for ATP synthesis, and export of ATP out to fuel the cell (By similarity). Cycles between the cytoplasmic-open state (c-state) and the matrix-open state (m-state): oper
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00153 Mito_carr 4 103 Mitochondrial carrier protein Family
PF00153 Mito_carr 109 206 Mitochondrial carrier protein Family
PF00153 Mito_carr 206 298 Mitochondrial carrier protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed in erythrocytes (at protein level). {ECO:0000269|PubMed:27641616}.
Sequence
Sequence length 298
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Calcium signaling pathway
cGMP-PKG signaling pathway
Necroptosis
Cellular senescence
Neutrophil extracellular trap formation
Alzheimer disease
Parkinson disease
Huntington disease
Spinocerebellar ataxia
Prion disease
Pathways of neurodegeneration - multiple diseases
Influenza A
Human T-cell leukemia virus 1 infection
Chemical carcinogenesis - reactive oxygen species
Diabetic cardiomyopathy
  Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization
Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
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)
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
Clear cell carcinoma of kidney Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GOUT GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INTELLECTUAL DISABILITY Disgenet, GenCC
Disgenet, GenCC
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Malignant lymphoma, large B-cell, diffuse Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 30397354, 35919504
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Associate 35288533
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 19140237
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Associate 30406146
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Associate 35288533
★☆☆☆☆
Found in Text Mining only
Esophageal Neoplasms Associate 35840882
★☆☆☆☆
Found in Text Mining only
Hypospadias Associate 32515122
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Associate 19140237
★☆☆☆☆
Found in Text Mining only
Myelodysplastic Syndromes Associate 33462268
★☆☆☆☆
Found in Text Mining only
Neoplasms Inhibit 35288533
★☆☆☆☆
Found in Text Mining only