1. Gene
  2. URM1 - ubiquitin related modifier 1 Gene

URM1 - ubiquitin related modifier 1 Gene

中文名称:泛素相关修饰符 1

种属: Homo sapiens

同用名: C9orf74

基因 ID: 81605 | 基因类型: protein coding

关于 URM1

Cytogenetic location: 9q34.11 Genomic coordinates (GRCh38): 9:128,371,319-128,392,016 (from NCBI)

This gene has 5 transcripts (splice variants) and 181 orthologues. Ubiquitous expression in spleen (RPKM 8.1), lymph node (RPKM 7.6) and 25 other tissues.

功能概要

启用硫载体活性。参与 tRNA 硫代修饰和 tRNA 摆动尿苷修饰。预测位于胞质溶胶中。预计活跃于核心。 [由基因组资源联盟提供,2022 年 4 月]

Enables sulfur carrier activity. Involved in tRNA thio-modification and tRNA wobble uridine modification. Predicted to be located in cytosol. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

URM1 基因产物(3)

mRNA Protein Name
NM_001135947.2 NP_001129419.1 ubiquitin-related modifier 1 isoform b
NM_001265582.1 NP_001252511.1 ubiquitin-related modifier 1 isoform c
NM_030914.4 NP_112176.1 ubiquitin-related modifier 1 isoform a
基因本体论
  • 分子功能
  • 生物过程
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
19017811 GOA
enables sulfur carrier activity IDA
IDA: 通过直接分析推断
19017811 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in tRNA thio-modification IMP
IMP: 通过突变表型推断
19017811 GOA
involved in tRNA wobble uridine modification IMP
IMP: 通过突变表型推断
19017811 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

URM1 蛋白结构

Urm1

Urm1: Urm1 (Ubiquitin related modifier) (6 - 101)

  • 0
  • 101 a.a.
蛋白主名 其他名称

ubiquitin-related modifier 1

ubiquitin-related modifier 1 homolog

URM1 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
URM1 Q9BTM9 USP15 Homo sapiens Q9Y4E8 21209336
种属内
URM1 Q9BTM9 CTU1 Homo sapiens Q7Z7A3 21209336
种属内
URM1 Q9BTM9 CTU1 Homo sapiens Q7Z7A3 19017811
种属内
URM1 Q9BTM9 CTU1 Homo sapiens Q7Z7A3 19017811
种属内
URM1 Q9BTM9 CSE1L Homo sapiens P55060 21209336
种属内
URM1 Q9BTM9 MOCS3 Homo sapiens O95396 21209336
种属内
URM1 Q9BTM9 MOCS3 Homo sapiens O95396 21209336
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, Hereditary Sensory And Autonomic, Type Iii

Familial Dysautonomia

Riley-Day Syndrome

Dysautonomia, Familial

HSAN3

Hsan Iii

Fd

Hereditary Sensory And Autonomic Neuropathy Type Iii

Dys

Hereditary Sensory And Autonomic Neuropathy 3

Riley Day Syndrome

Familial Autonomic Nervous Dysfunction

Hereditary Sensory Autonomic Neuropathy Type Iii

Hsan 3

Hsn 3

Hereditary Sensory Neuropathy Type 3

Hsan Type Iii

Hsn-Iii

Hereditary Sensory And Autonomic Neuropathy Type 3

Neuropathy, Hereditary Sensory And Autonomic, 3

Hsn Iii

Dysautonomia Familial

Neuropathy, Sensory And Autonomic, Hereditary, Type Iii

Hsan3 - [Hereditary Sensory And Autonomic Neuropathy Type 3]

Benign Epilepsy With Centrotemporal Spikes

Rolandic Epilepsy

Benign Rolandic Epilepsy

Epilepsy, Rolandic

Bcects

Benign Childhood Epilepsy With Centrotemporal Spike

Sylvan Seizures

Becrs

Bects

Bre

Benign Epilepsy Of Childhood With Centrotemporal Spikes

Benign Familial Epilepsy Of Childhood With Rolandic Spikes

Centrotemporal Epilepsy

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
Macaca mulatta URM1 VGNC VGNC:79704
Bos taurus URM1 VGNC VGNC:36699
Mus musculus URM1 MGD MGI:1915455
Rattus norvegicus URM1 RGD RGD:1306599
Felis catus URM1 VGNC VGNC:66854
Canis familiaris URM1 VGNC VGNC:48167
Others URM1 NCBI