1. Gene
  2. NCOA5 - nuclear receptor coactivator 5 Gene

NCOA5 - nuclear receptor coactivator 5 Gene

中文名称:核受体共激活因子 5

种属: Homo sapiens

同用名: CIA; bA465L10.6

基因 ID: 57727 | 基因类型: protein coding

关于 NCOA5

Cytogenetic location: 20q13.12 Genomic coordinates (GRCh38): 20:46,060,991-46,089,962 (from NCBI)

This gene has 2 transcripts (splice variants) and 202 orthologues. Ubiquitous expression in testis (RPKM 19.7), ovary (RPKM 15.7) and 25 other tissues.

功能概要

该基因编码 alpha 和 beta 雌激素受体以及孤儿核受体 NR1D2 的共同调节因子。该蛋白质定位于细胞核,被认为具有共激活因子和辅抑制因子功能。它与核受体的相互作用独立于受体上的 AF2 结构域,众所周知,AF2 结构域调节与其他辅助受体的相互作用。已发现该基因的几种可变剪接转录物变体。[RefSeq 提供,2017 年 1 月]

This gene encodes a coregulator for the alpha and beta estrogen receptors and the Orphan Nuclear Receptor NR1D2. The protein localizes to the nucleus, and is thought to have both coactivator and corepressor functions. Its interaction with nuclear receptors is independent of the AF2 domain on the receptors, which is known to regulate interaction with Other coreceptors. Several alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2017]

NCOA5 基因产物(5)

mRNA Protein Name
NM_001348148.2 NP_001335077.1 nuclear receptor coactivator 5 isoform 2
NM_001348149.2 NP_001335078.1 nuclear receptor coactivator 5 isoform 3
NM_001348150.2 NP_001335079.1 nuclear receptor coactivator 5 isoform 4
NM_001348151.2 NP_001335080.1 nuclear receptor coactivator 5 isoform 5
NM_020967.3 NP_066018.1 nuclear receptor coactivator 5 isoform 1
基因本体论
  • 分子功能
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
11113208 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

nuclear receptor coactivator 5

NCoA-5

关联疾病

疾病名称 别名
Night Blindness, Congenital Stationary, Type 1d

Congenital Stationary Night Blindness 1d

CSNB1D

Csnb, Complete, Autosomal Recessive

Night Blindness, Congenital Stationary , 1d, Autosomal Recessive

Congenital Stationary Night Blindness 1d Autosomal Recessive

Night Blindness, Congenital Stationary, 1d

Complete Autosomal Recessive Csnb

Blindness, Night, Stationary, Congenital, Type 1d

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
Bos taurus NCOA5 VGNC VGNC:31923
Macaca mulatta NCOA5 VGNC VGNC:74966
Felis catus NCOA5 VGNC VGNC:63741
Canis familiaris NCOA5 VGNC VGNC:43662
Rattus norvegicus NCOA5 RGD RGD:1307702
Mus musculus NCOA5 MGD MGI:2385165