1. Gene
  2. MRRF - mitochondrial ribosome recycling factor Gene

MRRF - mitochondrial ribosome recycling factor Gene

中文名称:线粒体核糖体循环因子

种属: Homo sapiens

同用名: RRF; MRFF; MTRRF

基因 ID: 92399 | 基因类型: protein coding

关于 MRRF

Cytogenetic location: 9q33.2 Genomic coordinates (GRCh38): 9:122,264,882-122,331,337 (from NCBI)

This gene has 12 transcripts (splice variants) and 203 orthologues. Ubiquitous expression in testis (RPKM 8.8), duodenum (RPKM 7.8) and 25 other tissues.

功能概要

该基因编码核糖体回收因子,它是线粒体翻译机制的一个组成部分。编码的蛋白质与线粒体延伸因子 2 一起,通过介导核糖体从信使 RNA 的分解,在线粒体翻译终止时在核糖体循环中发挥作用。已在 X 染色体上鉴定出该基因的假基因。[RefSeq 提供,2016 年 10 月]

This gene encodes a ribosome recycling factor, which is a component of the mitochondrial translational machinery. The encoded protein, along with mitochondrial elongation factor 2, functions in ribosomal recycling at the termination of mitochondrial translation by mediating the disassembly of ribosomes from messenger RNA. A pseudogene of this gene has been identified on chromosome X. [provided by RefSeq, Oct 2016]

MRRF 基因产物(8)

mRNA Protein Name
NM_001173512.3 NP_001166983.1 ribosome-recycling factor, mitochondrial isoform 3 precursor
NM_001346339.2 NP_001333268.1 ribosome-recycling factor, mitochondrial isoform 4
NM_001346341.2 NP_001333270.1 ribosome-recycling factor, mitochondrial isoform 1 precursor
NM_001346343.2 NP_001333272.1 ribosome-recycling factor, mitochondrial isoform 5
NM_001346345.2 NP_001333274.1 ribosome-recycling factor, mitochondrial isoform 6
NM_001346347.2 NP_001333276.1 ribosome-recycling factor, mitochondrial isoform 7
NM_138777.5 NP_620132.1 ribosome-recycling factor, mitochondrial isoform 1 precursor
NM_199177.4 NP_954646.1 ribosome-recycling factor, mitochondrial isoform 2 precursor
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
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
28514442 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in ribosome disassembly IDA
IDA: 通过直接分析推断
19716793 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
is active in mitochondrion IDA
IDA: 通过直接分析推断
18782833 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

MRRF 蛋白结构

RRF

RRF: Ribosome recycling factor (99 - 261)

  • 0
  • 100
  • 200
  • 262 a.a.
蛋白主名 其他名称

ribosome-recycling factor, mitochondrial

ribosome-releasing factor, mitochondrial

MRRF 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
Intra MRRF Q96E11 KRT40 Homo sapiens Q6A162
Y2H Prey Pooling
32296183
Intra MRRF Q96E11 KRT40 Homo sapiens Q6A162
Y2H Array
32296183
Intra MRRF Q96E11 FAM9B Homo sapiens Q8IZU0
Y2H Array
32296183
Intra MRRF Q96E11 FAM9B Homo sapiens Q8IZU0
Y2H Prey Pooling
32296183
Intra MRRF Q96E11 AGTRAP Homo sapiens Q6RW13-2
Y2H Prey Pooling
32296183
Intra MRRF Q96E11 AGTRAP Homo sapiens Q6RW13-2
Y2H Array
32296183
Intra MRRF Q96E11 CMTM5 Homo sapiens Q96DZ9-2
Y2H Prey Pooling
32296183
Intra MRRF Q96E11 CMTM5 Homo sapiens Q96DZ9-2
Y2H Array
32296183
Intra MRRF Q96E11 BANP Homo sapiens Q8N9N5-2
Y2H Prey Pooling
32296183
Intra MRRF Q96E11 BANP Homo sapiens Q8N9N5-2
Y2H Array
32296183
Intra MRRF Q96E11 WIPI2 Homo sapiens Q9Y4P8-4
Validated Y2H
32296183
Intra MRRF Q96E11 WIPI2 Homo sapiens Q9Y4P8-4
Y2H Array
32296183
Intra MRRF Q96E11 WIPI2 Homo sapiens Q9Y4P8-4
Y2H Prey Pooling
32296183
Intra MRRF Q96E11 ZNF408 Homo sapiens Q9H9D4
Y2H Array
32296183
Intra MRRF Q96E11 ZNF408 Homo sapiens Q9H9D4
Y2H Prey Pooling
32296183
Intra MRRF Q96E11 ZNF408 Homo sapiens Q9H9D4
Validated Y2H
32296183
Intra MRRF Q96E11 DBT Homo sapiens P11182
Anti Tag CoIP
28514442
Intra MRRF Q96E11 DBT Homo sapiens P11182
Anti Tag CoIP
33961781
Intra MRRF Q96E11 FHL3 Homo sapiens Q13643
Y2H Array
32296183
Intra MRRF Q96E11 FHL3 Homo sapiens Q13643
Y2H Prey Pooling
32296183
Intra MRRF Q96E11 SYP Homo sapiens P08247
Y2H Prey Pooling
32296183
Intra MRRF Q96E11 SYP Homo sapiens P08247
Y2H Array
32296183
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
Kearns-Sayre Syndrome

Ophthalmoplegia

Mitochondrial Cytopathy

KSS

Ophthalmoplegia, Pigmentary Degeneration Of Retina, And Cardiomyopathy

Oculocraniosomatic Syndrome

Chronic Progressive External Ophthalmoplegia With Myopathy

Cpeo With Myopathy

Total Ophthalmoplegia

Ophthalmoplegia-Plus Syndrome

Ophthalmoplegia, Progressive External, With Ragged-Red Fibers

Cpeo With Ragged-Red Fibers

Oculomotor Paralysis

Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication O

Renal Tubulopathy, Diabetes Mellitus, And Cerebellar Ataxia Due To Duplication Of Mitochondrial Dna

Proximal Tubulopathy, Diabetes Mellitus And Cerebellar Ataxia

Cpeo With Ragged Red Fibers

Ophthalmoplegia Plus Syndrome

Ophthalmoplegia, Progressive External, With Ragged Red Fibers

Kearns-Sayre Mitochondrial Cytopathy

Mitochondrial Myopathies

Uremic Neuropathy
Sensory Ataxic Neuropathy, Dysarthria, And Ophthalmoparesis

SANDO

Mitochondrial Recessive Ataxia Syndrome

Spinocerebellar Ataxia With Epilepsy

Epilepsy, Progressive Myoclonic 5

Epm5

Miras

SCAE

Sensory Ataxic Neuropathy With Mitochondrial Dna Deletions, Autosomal Recessive

Autosomal Recessive Sensory Ataxic Neuropathy With Mitochondrial Dna Deletions

Progressive Myoclonic Epilepsy Type 5

Pme Type 5

Progressive Myoclonus Epilepsy Type 5

Sensory Ataxic Neuropathy-Dysarthria-Ophthalmoparesis Syndrome

Recessive Mitochondrial Ataxia Syndrome

Sensory Ataxic Neuropathy Dysarthria And Ophthalmoparesis

Mitochondrial Spinocerebellar Ataxia-Epilepsy Syndrome

Mscae

Sensory Ataxic Neuropathy With Mitochondrial Dna Deletions Autosomal Recessive

Progressive Myoclonic Epilepsy With Sensory Ataxic Neuropathy

Epilepsy, Progressive Myoclonic, 5

Ataxia Neuropathy Spectrum

Chronic Progressive External Ophthalmoplegia

Progressive External Ophthalmoplegia

Cpeo

Peo

Ophthalmoplegia, Chronic Progressive External

Ophthalmoplegia, External, Progressive, Chronic

Graefe Disease

Peo - [Progressive External Ophthalmoplegia]

Ophthalmoplegia Plus Syndrome

Myoclonic Epilepsy Associated With Ragged-Red Fibers

Merrf Syndrome

MERRF

Fukuhara Syndrome

Myoclonic Epilepsy Associated With Ragged Red Fibers

Myoencephalopathy Ragged-Red Fiber Disease

Myoclonic Epilepsy - Ragged Red Fibers

Myoclonus Epilepsy And Ragged Red Fibers

Myoclonus With Epilepsy And With Ragged Red Fibers

Myoclonic Epilepsy With Ragged Red Fibers

Myoclonic Epilepsy With Ragged-Red Fibers

Fukuhara Disease

Myoclonus Epilepsy Associated With Ragged-Red Fibres

Myoclonus With Epilepsy With Ragged Red Fibers

Mitochondrial Myopathy

Mitochondrial Myopathies

Mitochondrial Cytopathy

Myopathies In Mitochondrial Disorders

Mitochondrial Encephalomyopathy

Mitochondrial Encephalomyopathies

Encephalomyopathy, Mitochondrial

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes

Melas Syndrome

MELAS

Mitochondrial Encephalomyopathy Lactic Acidosis And Stroke-Like Episodes

Mitochondrial Myopathy, Lactic Acidosis, Stroke-Like Episode

Mitochondrial Encephalomyopathy, Lactic Acidosis, And Stroke-Like Episodes

Myopathy, Mitochondrial-Encephalopathy-Lactic Acidosis-Stroke

Mitochondrial Encephalomyopathy, Lactic Acidosis And Stroke-Like Episodes

Mitochondrial Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes

Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis And Stroke-Like Episodes

Mitochondrial Encephalomyopathy With Lactic Acidosis And Stroke-Like Episodes Syndrome

Myopathy, Mitochondrial, Encephalopathy, Lactic Acidosis, And Stroke-Like Episodes

Leigh Syndrome

Leigh Disease

Infantile Subacute Necrotizing Encephalopathy

Leigh Syndrome Due To Mitochondrial Complex Iv Deficiency

LS

Sne

Leigh'S Disease

Leigh Syndrome Due To Mitochondrial Complex I Deficiency

Necrotizing Encephalopathy, Infantile Subacute, Of Leigh

Subacute Necrotizing Encephalomyelopathy

Necrotizing Encephalopathy Infantile Subacute Of Leigh

Leigh Syndrome Due To Mitochondrial Complex Iii Deficiency

Infantile Necrotizing Encephalomyelopathy

Juvenile Subacute Necrotizing Encephalomyelopathy

Leigh'S Necrotizing Encephalopathy

Subacute Necrotizing Encephalopathy

Juvenile Subacute Necrotizing Encephalopathy

Leigh Syndrome Due To Mitochondrial Complex Ii Deficiency

Leigh Syndrome Due To Mitochondrial Complex V Deficiency

Encephalopathy, Subacute Necrotizing, Infantile

Encephalopathy, Subacute Necrotizing, Juvenile

Maternally Inherited Leigh Syndrome

Subacute Necrotising Encephalomyelopathy

Subacute Necrotising Encephalopathy

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
Mus musculus MRRF MGD MGI:1915121
Rattus norvegicus MRRF RGD RGD:1305897
Canis familiaris MRRF VGNC VGNC:43428
Macaca mulatta MRRF VGNC VGNC:74927
Bos taurus MRRF VGNC VGNC:102827