1. Gene
  2. EVI2A - ecotropic viral integration site 2A Gene

EVI2A - ecotropic viral integration site 2A Gene

中文名称:亲嗜性病毒整合位点 2A

种属: Homo sapiens

同用名: EVDA; EVI2; EVI-2A

基因 ID: 2123 | 基因类型: protein coding

关于 EVI2A

Cytogenetic location: 17q11.2 Genomic coordinates (GRCh38): 17:31,316,410-31,321,622 (from NCBI)

This gene has 3 transcripts (splice variants) and 110 orthologues. Broad expression in brain (RPKM 20.1), appendix (RPKM 18.9) and 18 other tissues.

功能概要

预计是膜的组成部分。 [由基因组资源联盟提供,2022 年 4 月]

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

EVI2A 基因产物(2)

mRNA Protein Name
NM_001003927.3 NP_001003927.1 protein EVI2A isoform 1
NM_014210.4 NP_055025.2 protein EVI2A isoform 2 precursor
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
32296183 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

EVI2A 蛋白结构

EVI2A

EVI2A: Ectropic viral integration site 2A protein (EVI2A) (5 - 231)

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

protein EVI2A

ecotropic viral integration site 2A protein homolog

重组 EVI2A 蛋白

目录号 产品名 蛋白编号 纯度
HY-P75757 EVI2A Protein, Human (HEK293, Fc) P22794-1/NP_055025.2 (N31-M133) ≥95%

关联疾病

疾病名称 别名
Chromosome 17q11.2 Deletion Syndrome

Nf1 Microdeletion Syndrome

17q11 Microdeletion Syndrome

Neurofibromatosis Type 1 Microdeletion Syndrome

Van Asperen Syndrome

Del(17)(Q11)

Monosomy 17q11

Chromosome 17q11.2 Deletion Syndrome, 1.4mb

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 EVI2A RGD RGD:1593824
Mus musculus EVI2A MGD MGI:95458