1. Gene
  2. Vcp - valosin-containing protein Gene

Vcp - valosin-containing protein Gene

中文名称:含缬酪肽蛋白

种属: Rattus norvegicus

基因 ID: 116643 | 基因类型: protein coding

关于 Vcp

Primary_assembly 5: 57,210,168-57,229,571 reverse strand.mRatBN7.2:CM026978.1

This gene has 1 transcript (splice variant), 229 orthologues, 6 paralogues and is associated with 25 phenotypes. Biased expression in Heart (RPKM 1161.1), Muscle (RPKM 181.6) and 9 other tissues.

功能概要

该基因编码的蛋白可启动 ATP 水解活性;腺苷核糖核苷酸结合活性;和相同的蛋白质结合活性。参与内质网到高尔基体小泡介导的转运;泛素依赖性蛋白质分解代谢过程的正调控;和突触组织的调节。位于胞质溶胶和内质网中。 VCP-NPL4-UFD1 AAA ATPase 复合体和 VCP-NSFL1C 复合体的一部分。在谷氨酸能突触中活跃。该基因的人类直系同源基因与多种疾病有关,包括 Charcot-Marie-Tooth 病 2Y 型;佩吉特骨病;肌萎缩侧索硬化 14 型;伴有或不伴有额颞叶痴呆的早发性佩吉特骨病的包涵体肌病 1;和包涵体肌炎。与人类 VCP(含缬乐肽的蛋白质)同源。 [由基因组资源联盟提供,2022 年 4 月]

Enables ATP hydrolysis activity; adenyl ribonucleotide binding activity; and identical protein binding activity. Involved in endoplasmic reticulum to Golgi vesicle-mediated transport; positive regulation of ubiquitin-dependent protein catabolic process; and regulation of synapse organization. Located in cytosol and endoplasmic reticulum. Part of VCP-NPL4-UFD1 AAA ATPase complex and VCP-NSFL1C complex. Is active in glutamatergic synapse. Human ortholog(s) of this gene implicated in several diseases, including Charcot-Marie-Tooth disease type 2Y; Paget's disease of bone; amyotrophic lateral sclerosis type 14; inclusion body myopathy with early-onset Paget disease of bone with or without frontotemporal dementia 1; and inclusion body myositis. Orthologous to human VCP (valosin containing protein). [provided by Alliance of Genome Resources, Apr 2022]

Vcp 基因产物(1)

mRNA Protein Name
NM_053864.2 NP_446316.1 transitional endoplasmic reticulum ATPase

Vcp 蛋白结构

CDC48

CDC48: cl36852 (24 - 763)

  • 0
  • 200
  • 400
  • 600
  • 806 a.a.
蛋白主名 其他名称

transitional endoplasmic reticulum ATPase

15S Mg(2+)-ATPase p97 subunit

TER ATPase

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Vcp NCBI NCBI:7415