1. Gene
  2. RNF187 - ring finger protein 187 Gene

RNF187 - ring finger protein 187 Gene

中文名称:无名指蛋白 187

种属: Homo sapiens

同用名: RACO1; RACO-1

基因 ID: 149603 | 基因类型: protein coding

关于 RNF187

Cytogenetic location: 1q42.13 Genomic coordinates (GRCh38): 1:228,487,382-228,496,188 (from NCBI)

This gene has 2 transcripts (splice variants), 1 gene allele and 64 orthologues. Ubiquitous expression in thyroid (RPKM 54.8), brain (RPKM 49.5) and 25 other tissues.

功能概要

启用泛素蛋白转移酶活性。参与转录的正调控,以 DNA 为模板;蛋白酶体介导的泛素依赖性蛋白质分解代谢过程;和蛋白质泛素化。位于细胞质和核质中。 [由基因组资源联盟提供,2022 年 4 月]

Enables ubiquitin-protein transferase activity. Involved in positive regulation of transcription, DNA-templated; proteasome-mediated ubiquitin-dependent protein catabolic process; and protein ubiquitination. Located in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

RNF187 基因产物(1)

mRNA Protein Name
NM_001010858.3 NP_001010858.2 E3 ubiquitin-protein ligase RNF187
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
20852630 GOA
enables ubiquitin-protein transferase activity IDA
IDA: 通过直接分析推断
20852630 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in positive regulation of DNA-templated transcription IMP
IMP: 通过突变表型推断
20852630 GOA
involved in proteasome-mediated ubiquitin-dependent protein catabolic process IMP
IMP: 通过突变表型推断
20852630 GOA
involved in protein K48-linked ubiquitination IMP
IMP: 通过突变表型推断
20852630 GOA
involved in protein autoubiquitination IDA
IDA: 通过直接分析推断
20852630 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytoplasm IDA
IDA: 通过直接分析推断
20852630 GOA
located in nucleus IDA
IDA: 通过直接分析推断
20852630 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
蛋白主名 其他名称

E3 ubiquitin-protein ligase RNF187

RING domain AP1 coactivator 1

RNF187 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
RNF187 Q5TA31 ZNF835 Homo sapiens Q9Y2P0 32296183
种属内
RNF187 Q5TA31 ZNF417 Homo sapiens Q8TAU3 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
Hypermobility Of Coccyx

Coccygeal Hypermobility Syndrome

Hypermobility Of The Coccyx

Klippel-Feil Syndrome 3
Kummell'S Disease

Traumatic Spondylopathy

Kummell Disease

Kummell'S Spondylitis

Kümmelll-Verneuil Disease

Kümmell Spondylitis

Kümmell Disease

Traumatic Spondylosis

Brown-Sequard Syndrome

Brown-Squard Syndrome

Hemicord Syndrome

Hemiparaplegic Syndrome

Hemispinal Cord Syndrome

Brown-Séquard Syndrome

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 RNF187 RGD RGD:1308636
Bos taurus RNF187 VGNC VGNC:50124
Macaca mulatta RNF187 VGNC VGNC:100059
Mus musculus RNF187 MGD MGI:1914224