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Gene Gene information from NCBI Gene database.
Entrez ID 293
Gene name Solute carrier family 25 member 6
Gene symbol SLC25A6
Synonyms (NCBI Gene)
AAC3ANTANT 2ANT 3ANT3ANT3Y
Chromosome X|Y
Chromosome location X;Y
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.
155 Show/Hide all (155)
miRTarBase ID miRNA Experiments Reference
MIRT031609 hsa-miR-16-5p Proteomics 18668040
MIRT042493 hsa-miR-423-3p CLASH 23622248
MIRT039389 hsa-miR-421 CLASH 23622248
MIRT1357437 hsa-miR-122 CLIP-seq
MIRT1357438 hsa-miR-1229 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19 Show/Hide all (19)
GO ID Ontology Definition Evidence Reference
GO:0005471 Function ATP:ADP antiporter activity IEA
GO:0005471 Function ATP:ADP antiporter activity NAS 2541251
GO:0005515 Function Protein binding IPI 16201016, 21370995, 21516116, 24725412, 25416956, 29128334, 29892012, 33961781
GO:0005634 Component Nucleus HDA 21630459
GO:0005739 Component Mitochondrion HDA 20833797
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300151 N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P12236
Protein name ADP/ATP translocase 3 (ADP,ATP carrier protein 3) (ADP,ATP carrier protein, isoform T2) (ANT 2) (Adenine nucleotide translocator 3) (ANT 3) (Solute carrier family 25 member 6) [Cleaved into: ADP/ATP translocase 3, 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 Pathway Reactome Pathway
Calcium signaling pathway Mitochondrial protein import
cGMP-PKG signaling pathway Influenza Virus Induced Apoptosis
Necroptosis Vpr-mediated induction of apoptosis by mitochondrial outer membrane permeabilization
Cellular senescence Transport of nucleosides and free purine and pyrimidine bases across the plasma membrane
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  
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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 Reference Evidence Score
Colon adenocarcinoma Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Lung cancer Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SLC25A6-related disorder Likely benign; Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Uterine corpus endometrial carcinoma Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Show/Hide Text Mining Associations (24)
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Aphasia Aphasia BEFREE 30778280
★★★★★
★☆☆☆☆
Found in Text Mining only
Bipolar Disorder Bipolar Disorder BEFREE 22980403
★★★★★
★☆☆☆☆
Found in Text Mining only
Bone Marrow Diseases Bone Marrow Diseases BEFREE 29916066
★★★★★
★☆☆☆☆
Found in Text Mining only
Breast Carcinoma Breast Carcinoma BEFREE 22524830
★★★★★
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Breast neoplasm Pubtator 20650008, 22198296 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 19715608 Stimulate
★★★★★
★☆☆☆☆
Found in Text Mining only
Carcinoma Renal Cell Renal cell carcinoma Pubtator 8781539 Inhibit
★★★★★
★☆☆☆☆
Found in Text Mining only
Cardiomyopathy Dilated Dilated cardiomyopathy Pubtator 10841224, 16107323, 1867322 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only
Cardiomyopathy, Familial Idiopathic Cardiomyopathy BEFREE 16107323
★★★★★
★☆☆☆☆
Found in Text Mining only
Graves Disease Graves disease Pubtator 8918809 Associate
★★★★★
★☆☆☆☆
Found in Text Mining only