1. Gene
  2. SLC25A11 - solute carrier family 25 member 11 Gene

SLC25A11 - solute carrier family 25 member 11 Gene

中文名称:溶质载体家族 25 成员 11

种属: Homo sapiens

同用名: OGC; PGL6; SLC20A4

基因 ID: 8402 | 基因类型: protein coding

关于 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.

功能概要

氧戊二酸/苹果酸载体将 2-氧戊二酸转运穿过线粒体的内膜,与苹果酸或其他二羧酸进行电中性交换 (Iacobazzi 等人总结,1992 [PubMed 1457818]) 。[OMIM 提供,2011 年 1 月]

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 基因产物(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
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
32814053 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

SLC25A11 蛋白结构

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
  • 314 a.a.
蛋白主名 其他名称

mitochondrial 2-oxoglutarate/malate carrier protein

OGCP

SLC25A11 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
SLC25A11 Q02978 NEK7 Homo sapiens Q8TDX7
Validated Y2H
32814053
种属内
SLC25A11 Q02978 NEK7 Homo sapiens Q8TDX7
Y2H Array
32814053
种属内
SLC25A11 Q02978 NEK7 Homo sapiens Q8TDX7
Y2H Pooling
32814053
种属内
SLC25A11 Q02978 AHCYL1 Homo sapiens O43865
Validated Y2H
32814053
种属内
SLC25A11 Q02978 AHCYL1 Homo sapiens O43865
Y2H Array
32814053
种属内
SLC25A11 Q02978 AHCYL1 Homo sapiens O43865
Y2H Pooling
32814053
种属内
SLC25A11 Q02978 DLST Homo sapiens P36957
Validated Y2H
32814053
种属内
SLC25A11 Q02978 DLST Homo sapiens P36957
Y2H Array
32814053
种属内
SLC25A11 Q02978 DLST Homo sapiens P36957
Y2H Pooling
32814053
种属内
SLC25A11 Q02978 SMIM26 Homo sapiens A0A096LP01
Anti Tag CoIP
37009826
种属内
SLC25A11 Q02978 CDH1 Homo sapiens P12830
Y2H Pooling
32814053
种属内
SLC25A11 Q02978 CDH1 Homo sapiens P12830
Y2H Array
32814053
种属内
SLC25A11 Q02978 CDH1 Homo sapiens P12830
Validated Y2H
32814053
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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