1. Gene
  2. RHOT2 - ras homolog family member T2 Gene

RHOT2 - ras homolog family member T2 Gene

中文名称:ras 同系物家族成员 T2

种属: Homo sapiens

同用名: RASL; ARHT2; MIRO2; MIRO-2; C16orf39

基因 ID: 89941 | 基因类型: protein coding

关于 RHOT2

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:668,083-674,174 (from NCBI)

This gene has 28 transcripts (splice variants), 195 orthologues and 22 paralogues. Ubiquitous expression in spleen (RPKM 20.5), duodenum (RPKM 16.0) and 25 other tissues.

功能概要

该基因编码 GTP 酶 Rho 家族的一个成员。编码的蛋白质定位于线粒体外膜,在线粒体运输和融合裂变动力学中发挥作用。[RefSeq 提供,2011 年 11 月]

This gene encodes a member of the Rho family of GTPases. The encoded protein is localized to the outer mitochondrial membrane and plays a role in mitochondrial trafficking and fusion-fission dynamics. [provided by RefSeq, Nov 2011]

RHOT2 基因产物(21)

mRNA Protein Name
NM_001352275.2 NP_001339204.1 mitochondrial Rho GTPase 2 isoform 1
NM_001352276.2 NP_001339205.1 mitochondrial Rho GTPase 2 isoform 3
NM_001352277.2 NP_001339206.1 mitochondrial Rho GTPase 2 isoform 4
NM_001352278.2 NP_001339207.1 mitochondrial Rho GTPase 2 isoform 5
NM_001352279.2 NP_001339208.1 mitochondrial Rho GTPase 2 isoform 6
NM_001352280.2 NP_001339209.1 mitochondrial Rho GTPase 2 isoform 7
NM_001352281.2 NP_001339210.1 mitochondrial Rho GTPase 2 isoform 8
NM_001352282.2 NP_001339211.1 mitochondrial Rho GTPase 2 isoform 8
NM_001352283.2 NP_001339212.1 mitochondrial Rho GTPase 2 isoform 9
NM_001352284.2 NP_001339213.1 mitochondrial Rho GTPase 2 isoform 10
NM_001352285.2 NP_001339214.1 mitochondrial Rho GTPase 2 isoform 11
NM_001352286.2 NP_001339215.1 mitochondrial Rho GTPase 2 isoform 12
NM_001352287.1 NP_001339216.1 mitochondrial Rho GTPase 2 isoform 13
NM_001352288.2 NP_001339217.1 mitochondrial Rho GTPase 2 isoform 13
NM_001352289.2 NP_001339218.1 mitochondrial Rho GTPase 2 isoform 13
NM_001352290.2 NP_001339219.1 mitochondrial Rho GTPase 2 isoform 13
NM_001352291.2 NP_001339220.1 mitochondrial Rho GTPase 2 isoform 13
NM_001352292.2 NP_001339221.1 mitochondrial Rho GTPase 2 isoform 13
NM_001352293.2 NP_001339222.1 mitochondrial Rho GTPase 2 isoform 13
NM_001352294.2 NP_001339223.1 mitochondrial Rho GTPase 2 isoform 13
NM_138769.3 NP_620124.1 mitochondrial Rho GTPase 2 isoform 2
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
16630562 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cellular homeostasis IMP
IMP: 通过突变表型推断
12482879 GOA
involved in mitochondrial outer membrane permeabilization IMP
IMP: 通过突变表型推断
12482879 GOA
involved in mitochondrion transport along microtubule IMP
IMP: 通过突变表型推断
16630562 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in mitochondrial outer membrane IDA
IDA: 通过直接分析推断
12482879 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

RHOT2 蛋白结构

Ras

Ras: Ras family (6 - 166)

EF_assoc_2

EF_assoc_2: EF hand associated (219 - 306)

EF_assoc_1

EF_assoc_1: EF hand associated (341 - 412)

Roc

Roc: Ras of Complex, Roc, domain of DAPkinase (420 - 527)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 618 a.a.
蛋白主名 其他名称

mitochondrial Rho GTPase 2

mitochondrial Rho (MIRO) GTPase 2

RHOT2 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
RHOT2 Q8IXI1 TRAK1 Homo sapiens Q9UPV9 16630562
种属内
RHOT2 Q8IXI1 TRAK1 Homo sapiens Q9UPV9 24995978
种属内
RHOT2 Q8IXI1 TMEM86B Homo sapiens Q8N661 32296183
种属内
RHOT2 Q8IXI1 TMEM86B Homo sapiens Q8N661 32296183
种属内
RHOT2 Q8IXI1 TMEM86B Homo sapiens Q8N661 32296183
种属内
RHOT2 Q8IXI1 SAR1A Homo sapiens Q9NR31 32296183
种属内
RHOT2 Q8IXI1 SAR1A Homo sapiens Q9NR31 32296183
种属内
RHOT2 Q8IXI1 SAR1A Homo sapiens Q9NR31 32296183
种属内
RHOT2 Q8IXI1 TMEM14B Homo sapiens Q9NUH8 32296183
种属内
RHOT2 Q8IXI1 TMEM14B Homo sapiens Q9NUH8 32296183
种属内
RHOT2 Q8IXI1 TMEM14B Homo sapiens Q9NUH8 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
Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive

Charcot-Marie-Tooth Disease Type 4

Charcot-Marie-Tooth Disease Type 4e

Hereditary Motor And Sensory Neuropathy

Cmt4e

CHN1

Hypomyelinating Neuropathy, Congenital, 1

Charcot-Marie-Tooth Neuropathy Type 4e

Neuropathy, Congenital Hypomyelinating, 1

Ar-Cmt1

Autosomal Recessive Demyelinating Charcot-Marie-Tooth

Cmt4

Neuropathy, Congenital Hypomyelinating Or Amyelinating, Autosomal Recessive

Hypomyelination, Severe Congenital

Charcot-Marie-Tooth Disease, Type 4e

Charcot-Marie-Tooth Neuropathy, Type 4e

Autosomal Recessive Congenital Hypomyelinating Or Amyelinating Neuropathy

Autosomal Recessive Congenital Hypomyelinating Neuropathy

Congenital Amyelinating Neuropathy

Congenital Hypomyelinating Neuropathy Autosomal Recessive

Neuropathy, Congenital Hypomyelinating Or Amyelinating

Severe Congenital Hypomyelination

Hereditary Sensory Motor Neuropathy

Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive

Neuropathy, Hypomyelinating, Congenital, Type 1

Neuropathy, Motor And Sensory, Hereditary

Congenital Hypomyelinating Neuropathy

Hereditary Motor And Sensory Neuropathies

Hereditary Sensorimotor Neuropathy

Hmsn - [Hereditary Motor And Sensory Neuropathy]

Hsmn - [Hereditary Sensory And Motor Neuropathy]

Hereditary Motor And Sensory Neuropathy, Types I-Iv

3-Methylglutaconic Aciduria, Type Iii

Optic Atrophy

3-Methylglutaconic Aciduria Type 3

Costeff Syndrome

Mga3

Costeff Optic Atrophy Syndrome

Optic Atrophy Plus Syndrome

Infantile Optic Atrophy With Chorea And Spastic Paraplegia

3-Methylglutaconic Aciduria Type Iii

Autosomal Recessive Optic Atrophy Plus Syndrome

Autosomal Recessive Optic Atrophy Type 3

Opa3 Defect

MGCA3

Mga, Type Iii

Iraqi Jewish Optic Atrophy Plus

Mga Type Iii

Optic Atrophy, Infantile, With Chorea And Spastic Paraplegia

Iraqi-Jewish 'Optic Atrophy Plus'

Optic Atrophy 3, Autosomal Recessive

Opa3, Autosomal Recessive

Opa3-Related 3-Methylglutaconic Aciduria

Iraqi-Jewish Optic Atrophy Plus

Atrophy Of Optic Disc

3-Alpha Methylglutaconic Aciduria Type Iii

Optic Atrophy 3

Optic Atrophy Infantile With Chorea And Spastic Paraplegia

Autosomal Recessive Opa3

Autosomal Recessive Optic Atrophy 3

3-Methylglutaconic Aciduria 3

3-Alpha-Methylglutaconic Aciduria Type 3

Optic Atrophy 3 Autosomal Recessive

Atrophy, Optic

Atrophy, Optic, Plus Syndrome

Optic Nerve Atrophy

Primary Optic Atrophy

Oa - [Optic Atrophy]

Second Cranial Nerve Atrophy

Second Cranium Nerve Atrophy

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 RHOT2 VGNC VGNC:45564
Bos taurus RHOT2 VGNC VGNC:33954
Macaca mulatta RHOT2 VGNC VGNC:76796
Rattus norvegicus RHOT2 RGD RGD:727970
Mus musculus RHOT2 MGD MGI:2384892
Felis catus RHOT2 VGNC VGNC:64618