1. Gene
  2. RNF125 - ring finger protein 125 Gene

RNF125 - ring finger protein 125 Gene

中文名称:无名指蛋白 125

种属: Homo sapiens

同用名: TNORS; TRAC1; TRAC-1

基因 ID: 54941 | 基因类型: protein coding

关于 RNF125

Cytogenetic location: 18q12.1 Genomic coordinates (GRCh38): 18:32,018,825-32,088,144 (from NCBI)

This gene has 5 transcripts (splice variants), 136 orthologues, 4 paralogues and is associated with 2 phenotypes. Ubiquitous expression in fat (RPKM 4.1), bone marrow (RPKM 4.0) and 25 other tissues.

功能概要

该基因编码一种新型 E3 泛素连接酶,该酶在 N 末端包含一个环指结构域,在 C 末端包含三个锌结合基序和一个泛素相互作用基序。作为豆蔻酰化的结果,该蛋白质与膜结合并且主要定位于细胞内膜系统。所编码的蛋白质可以作为 T 细胞受体信号通路中的正调节剂发挥作用。[RefSeq 提供,2012 年 3 月]

This gene encodes a novel E3 ubiquitin Ligase that contains a RING finger domain in the N-terminus and three zinc-binding and one ubiquitin-interacting motif in the C-terminus. As a result of myristoylation, this protein associates with membranes and is primarily localized to intracellular membrane systems. The encoded protein may function as a positive regulator in the T-cell receptor signaling pathway. [provided by RefSeq, Mar 2012]

RNF125 基因产物(1)

mRNA Protein Name
NM_017831.4 NP_060301.2 E3 ubiquitin-protein ligase RNF125
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 p53 binding IPI
IPI: 通过物理相互作用推断
25591766 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
17460044 GOA
enables ubiquitin conjugating enzyme binding IPI
IPI: 通过物理相互作用推断
27411375 GOA
enables ubiquitin protein ligase activity IDA
IDA: 通过直接分析推断
17460044 GOA
enables zinc ion binding IDA
IDA: 通过直接分析推断
27411375 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in negative regulation of RIG-I signaling pathway IDA
IDA: 通过直接分析推断
17460044 GOA
involved in negative regulation of type I interferon production IDA
IDA: 通过直接分析推断
17460044 GOA
involved in protein polyubiquitination IDA
IDA: 通过直接分析推断
27411375 GOA
involved in ubiquitin-dependent protein catabolic process IDA
IDA: 通过直接分析推断
17460044 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in Golgi membrane IDA
IDA: 通过直接分析推断
17990982 GOA
part of VCP-NPL4-UFD1 AAA ATPase complex IDA
IDA: 通过直接分析推断
26471729 GOA
located in intracellular membrane-bounded organelle IDA
IDA: 通过直接分析推断
17990982 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

RNF125 蛋白结构

zf-RING_2

zf-RING_2: Ring finger domain (36 - 76)

zf-Di19

zf-Di19: Drought induced 19 protein (Di19), zinc-binding (140 - 196)

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

E3 ubiquitin-protein ligase RNF125

T-cell RING activation protein 1

RNF125 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 RNF125 Q96EQ8 MAVS Homo sapiens Q7Z434-1
Anti Tag CoIP
17460044
Intra RNF125 Q96EQ8 RIGI Homo sapiens O95786-1
Anti Bait CoIP
17460044
Intra RNF125 Q96EQ8 RIGI Homo sapiens O95786-1
Anti Tag CoIP
17460044
Intra RNF125 Q96EQ8 UBE2E2 Homo sapiens Q96LR5
Y2H
17460044
Intra RNF125 Q96EQ8 UBE2E2 Homo sapiens Q96LR5
Anti Tag CoIP
17460044
Intra RNF125 Q96EQ8 VCP Homo sapiens P55072
Pull Down
26471729
Intra RNF125 Q96EQ8 VCP Homo sapiens P55072
Anti Bait CoIP
26471729
Intra RNF125 Q96EQ8 IFIH1 Homo sapiens Q9BYX4
Anti Tag CoIP
17460044
Intra RNF125 Q96EQ8 RIGI Homo sapiens O95786
Anti Bait CoIP
26471729
Intra RNF125 Q96EQ8 RIGI Homo sapiens O95786
Pull Down
26471729
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
Tenorio Syndrome

TNORS

Overgrowth, Macrocephaly, And Intellectual Disability Syndrome

Neuronopathy, Distal Hereditary Motor, Type Iid

HMN2D

Hmn Iid

Dhmn2d

Distal Hereditary Motor Neuronopathy Type 2d

Distal Hereditary Motor Neuropathy Type Iid

Neuronopathy, Distal Hereditary Motor, Type 2d

Neuropathy, Distal Hereditary Motor, Type Iid

Spinal Muscular Atrophy, Distal, Autosomal Dominant, Calf-Predominant

Distal Spinal Muscular Atrophy With Calf Predominance

Neuronopathy, Distal Hereditary Motor, 2d

Autosomal Dominant Spinal Muscular Atrophy Distal Calf-Predominant

Dhmn Iid

Neuropathy, Motor, Distal, Hereditary, Type 2d

Distal Hereditary Motor Neuronopathy Type 2

Distal Hereditary Motor Neuropathy, Type Ii

Distal Hereditary Motor Neuropathy Type 2

Distal Hereditary Motor Neuropathy Type Ii

Hmn Ii

Hmn2

Distal Hereditary Motor Neuronopathy, Type Ii

Distal Spinal Muscular Atrophy Type 2

Dhmn2

Dsma2

Neuropathy, Motor, Distal, Hereditary, Type Ii

Spinal Muscular Atrophy, Jerash Type

Non-Syndromic X-Linked Intellectual Disability

X-Linked Non-Syndromic Intellectual Disability

Non-Specific X-Linked Mental Retardation

X-Linked Non-Specific Intellectual Disability

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
Rattus norvegicus RNF125 RGD RGD:1306757
Felis catus RNF125 VGNC VGNC:64667
Mus musculus RNF125 MGD MGI:1914914
Canis familiaris RNF125 VGNC VGNC:45627
Macaca mulatta RNF125 VGNC VGNC:104244
Bos taurus RNF125 VGNC VGNC:34017