1. Gene
  2. SLC25A5 - solute carrier family 25 member 5 Gene

SLC25A5 - solute carrier family 25 member 5 Gene

Homo sapiens

Also known as T2; T3; 2F1; AAC2; ANT2

Gene ID: 292 | Gene type: protein coding

About SLC25A5

Cytogenetic location: Xq24 Genomic coordinates (GRCh38): X:119,468,444-119,471,396 (from NCBI)

This gene has 4 transcripts (splice variants), 202 orthologues and 49 paralogues. Ubiquitous expression in duodenum (RPKM 370.1), small intestine (RPKM 299.2) and 25 other tissues.

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 into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Suppressed expression of this gene has been shown to induce Apoptosis and inhibit tumor growth. The human genome contains several non-transcribed pseudogenes of this gene.[provided by RefSeq, Jun 2013]

SLC25A5 Products(1)

mRNA Protein Name
NM_001152.5 NP_001143.2 ADP/ATP translocase 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables adenine nucleotide transmembrane transporter activity IMP
IMP: Inferred from mutant phenotype
19116139 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17715127 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
19725078 GOA
Biological Process GO Annotation Evidence Reference Source
involved in adenine nucleotide transport IMP
IMP: Inferred from mutant phenotype
19116139 GOA
involved in negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway IMP
IMP: Inferred from mutant phenotype
19154410 GOA
involved in positive regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
19154410 GOA
Cellular Component GO Annotation Evidence Reference Source
part of MMXD complex IDA
IDA: Inferred from direct assay
20797633 GOA
located in membrane IDA
IDA: Inferred from direct assay
27641616 GOA
located in mitochondrial nucleoid IDA
IDA: Inferred from direct assay
18063578 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SLC25A5 Protein Structure

Mito_carr

Mito_carr: Mitochondrial carrier protein (6 - 99)

Mito_carr

Mito_carr: Mitochondrial carrier protein (111 - 203)

Mito_carr

Mito_carr: Mitochondrial carrier protein (209 - 297)

  • 0
  • 100
  • 200
  • 298 a.a.
Protein Preferred Names Protein Names

ADP/ATP translocase 2

adenine nucleotide translocator 2 (fibroblast)

SLC25A5 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
SLC25A5 P05141 SIRT4 Homo sapiens Q9Y6E7
Anti Tag CoIP
17715127
Intra
SLC25A5 P05141 LRRK2 Homo sapiens Q5S007
Anti Tag CoIP
21370995
Intra
SLC25A5 P05141 SLC35F6 Homo sapiens Q8N357
Anti Tag CoIP
19154410
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Oncocytoma

Oxyphilic Adenoma

Follicular Adenoma, Oxyphilic Cell

Adenoma, Oxyphilic

Hurthle Cell Tumor

Oncocytic Neoplasm

Hypertension And Brachydactyly Syndrome

Brachydactyly With Hypertension

Bilginturan Syndrome

HTNB

Brachydactyly-Arterial Hypertension Syndrome

Brachydactyly, Type E, With Short Stature And Hypertension

Bilginturan Brachydactyly

Brachydactyly Type E With Short Stature And Hypertension

Type E Brachydactyly With Short Stature And Hypertension

Brachydactyly Type E, With Short Stature And Hypertension

Hypertension With Brachydactyly

Dilated Cardiomyopathy

Familial Dilated Cardiomyopathy

Primary Dilated Cardiomyopathy

Idiopathic Dilated Cardiomyopathy

Congestive Cardiomyopathy

Idiopathic Dilation Cardiomyopathy

Primary Familial Dilated Cardiomyopathy

Cardiomyopathy, Dilated

DCM

Cardiomyopathy, Familial Dilated

Dilated Cardiomyopathy, Familial

Hypokinetic Dilated Cardiomyopathy, Familial

Familial Idiopathic Cardiomyopathy

Fdc

Cardiomyopathy, Familial Idiopathic

Idiopathic Cardiomegaly

Dilated Congestive Cardiomyopathy

Chronic Dilated Cardiomyopathy

Ccm - [Congestive Cardiomyopathy]

Cocm - [Congestive Cardiomyopathy]

Dcm - [Dilated Cardiomyopathy]

Dilated-Hypokinetic Cardiomyopathy

Congestive Idiopathic Cardiomyopathy

Primary Idiopathic Dilated Cardiomyopathy

Bubonic Plague

Black Death

Plague, Bubonic

Plague, Septicemic

Pestis Bubonica

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Canis familiaris SLC25A5 VGNC VGNC:54599
Rattus norvegicus SLC25A5 RGD RGD:620353
Bos taurus SLC25A5 VGNC VGNC:49966
Mus musculus SLC25A5 MGD MGI:1353496
Others SLC25A5 NCBI