SLC25A11 - solute carrier family 25 member 11 Gene

Also Known as OGC; PGL6; SLC20A4

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 8402

About SLC25A11

Cytogenetic location: 17p13.2 Genomic coordinates (GRCh38): 17:4,937,130-4,940,046 (from NCBI)

This gene has 5 transcripts (splice variants), 184 orthologues, 49 paralogues and is associated with 2 phenotypes. Ubiquitous expression in heart (RPKM 61.1), kidney (RPKM 32.4) and 24 other tissues.

Summary

The oxoglutarate/malate carrier transports 2-oxoglutarate across the inner membranes of mitochondria in an electroneutral exchange for malate or Other dicarboxylic acids (summary by Iacobazzi et al., 1992 [PubMed 1457818]).[supplied by OMIM, Jan 2011]

SLC25A11 Products (3)

mRNA Protein Name
NM_001165417.2 NP_001158889.1 mitochondrial 2-oxoglutarate/malate carrier protein isoform 2
NM_001165418.2 NP_001158890.1 mitochondrial 2-oxoglutarate/malate carrier protein isoform 3
NM_003562.5 NP_003553.2 mitochondrial 2-oxoglutarate/malate carrier protein isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
32814053 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

SLC25A11 Protein Structure

Mito_carr

Mito_carr: Mitochondrial carrier protein (23 - 106)

Mito_carr

Mito_carr: Mitochondrial carrier protein (117 - 211)

Mito_carr

Mito_carr: Mitochondrial carrier protein (218 - 308)

  • 0
  • 100
  • 200
  • 300
  • 314 a.a.
Protein Preferred Names Protein Names

mitochondrial 2-oxoglutarate/malate carrier protein

  • OGCP

SLC25A11 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SLC25A11 Q02978 NEK7 Homo sapiens Q8TDX7 32814053
Intra
SLC25A11 Q02978 NEK7 Homo sapiens Q8TDX7 32814053
Intra
SLC25A11 Q02978 NEK7 Homo sapiens Q8TDX7 32814053
Intra
SLC25A11 Q02978 AHCYL1 Homo sapiens O43865 32814053
Intra
SLC25A11 Q02978 AHCYL1 Homo sapiens O43865 32814053
Intra
SLC25A11 Q02978 AHCYL1 Homo sapiens O43865 32814053
Intra
SLC25A11 Q02978 DLST Homo sapiens P36957 32814053
Intra
SLC25A11 Q02978 DLST Homo sapiens P36957 32814053
Intra
SLC25A11 Q02978 DLST Homo sapiens P36957 32814053
Intra
SLC25A11 Q02978 SMIM26 Homo sapiens A0A096LP01 37009826
Intra
SLC25A11 Q02978 CDH1 Homo sapiens P12830 32814053
Intra
SLC25A11 Q02978 CDH1 Homo sapiens P12830 32814053
Intra
SLC25A11 Q02978 CDH1 Homo sapiens P12830 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Paragangliomas 6
  • PGL6

Hereditary Paraganglioma-Pheochromocytoma Syndromes
  • Hereditary Pheochromocytoma-Paraganglioma

  • Hereditary Paraganglioma-Pheochromocytoma

  • Familial Pheochromocytoma-Paraganglioma

  • Paragangliomas 2

  • Paragangliomas 3

  • Paragangliomas 4

  • Sdhx-Related Paraganglioma-Pheochromocytoma

  • Familial Paraganglioma Syndrome

  • Familial Paraganglioma-Pheochromocytoma Syndromes

  • Fpgl

  • Fpgl/Pheo

  • Paragangliomas 1

  • Paraganglioma

Breast Leiomyosarcoma
  • Leiomyosarcoma Of The Breast

Oculogyric Crisis
Aromatic L-Amino Acid Decarboxylase Deficiency
  • Aadc Deficiency

  • Dopa Decarboxylase Deficiency

  • Ddc Deficiency

  • Aromatic Amino Acid Decarboxylase Deficiency

  • Deficiency Of Aromatic-L-Amino-Acid Decarboxylase

  • AADCD

  • Aromatic-L-Amino-Acid Decarboxylase Deficiency

  • Aromatic L-Amino-Acid Decarboxylase Deficiency

Developmental And Epileptic Encephalopathy 39
  • Hypomyelination, Global Cerebral

  • Agc1 Deficiency

  • Epileptic Encephalopathy, Early Infantile, 39

  • DEE39

  • Eiee39

  • Aspartate-Glutamate Carrier 1 Deficiency

  • Epileptic Encephalopathy With Global Cerebral Demyelination

  • Developmental And Epileptic Encephalopathy, 39

  • Early Infantile Epileptic Encephalopathy 39

  • Mitochondrial Aspartate-Glutamate Carrier 1 Deficiency

  • Global Cerebral Hypomyelination

  • Hereditary Central Nervous System Demyelinating Diseases

Lung Giant Cell Carcinoma
  • Carcinoma, Giant Cell

  • Giant Cell Carcinoma

  • Giant Cell Lung Carcinoma

  • Carcinoma Giant Cell

  • Giant Cell Carcinoma Of Lung

Persistent Generalized Lymphadenopathy
  • Pgl

  • Persistant Generalized Lymphadenopathy

Postencephalitic Parkinson Disease
  • Postencephalitic Parkinsonism

  • Parkinson Disease, Postencephalitic

Pancreatic Mucinous Cystadenoma
  • Pancreatic Mucinous Cystic Neoplasm

  • Pancreatic Mucinous-Cystic Neoplasm

Citrullinemia, Type Ii, Adult-Onset
  • Citrin Deficiency

  • CTLN2

  • Citrullinemia Type Ii

  • Adult-Onset Citrullinemia Type 2

  • Adult-Onset Type Ii Citrullinemia

  • Citrullinemia, Adult-Onset Type Ii

  • Adult-Onset Citrin Deficiency

  • Adult-Onset Citrullinemia Type Ii

  • Citrullinemia Type 2

  • Citrullinemia 2

  • Citrullinemia, Type Ii

Hyperphenylalaninemia, Bh4-Deficient, A
  • 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency

  • Pts Deficiency

  • HPABH4A

  • Hyperphenylalaninemia, Tetrahydrobiopterin-Deficient, Due To Pts Deficiency

  • Ptsd

  • Bh4-Deficient Hyperphenylalaninemia A

  • Hyperphenylalaninemia Due To 6-Pyruvoyltetrahydropterin Synthase Deficiency

  • Tetrahydobioperin-Deficient Hyperphenylalaninemia Due To Pts Deficiency

  • Hyperphenylalanemia, Bh4-Deficient, A

  • Hyperphenylalaninemia Due To 6-Pyruvoyl-Tetrahydropterin Synthase Deficiency

  • 6-Pyruvoyltetrahydropterin Synthase Deficiency

  • Hyperphenylalaninemia Tetrahydrobiopterin-Deficient Due To Pts Deficiency

  • Ptpsd

  • Hyperphenylalaninemia, Bh4-Deficient, Type A

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 SLC25A11 VGNC VGNC:46291
Macaca mulatta SLC25A11 VGNC VGNC:77429
Mus musculus SLC25A11 MGD MGI:1915113
Bos taurus SLC25A11 VGNC VGNC:34742
Felis catus SLC25A11 VGNC VGNC:65253
Rattus norvegicus SLC25A11 RGD RGD:708476
Others SLC25A11 NCBI