1. Gene
  2. Vsx2 - visual system homeobox 2 Gene

Vsx2 - visual system homeobox 2 Gene

种属: Mus musculus

同用名: or; Chx10; Hox10; Hox-10

基因 ID: 12677 | 基因类型: protein coding

关于 Vsx2

功能概要

This gene encodes a member of the Vsx (visual system homeobox) family which belongs to the larger PRD homeobox class. The encoded protein is required for eye organogenesis and controls retinal development. Disruption of this gene is associated with ocular retardation J (orJ), a mouse disease which causes microphthalmia, retinal degeneration and optic nerve aplasia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2014]

Vsx2 基因产物(2)

mRNA Protein Name
NM_001301427.1 NP_001288356.1 visual system homeobox 2 isoform 1
NM_007701.3 NP_031727.1 visual system homeobox 2 isoform 2
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
9464541 MGI
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
15767664 MGI
located in intracellular anatomical structure IDA
IDA: 通过直接分析推断
10482234 MGI
located in nucleus IDA
IDA: 通过直接分析推断
15767664 MGI
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

visual system homeobox 2

C. elegans ceh-10 homeo domain containing homolog

ceh-10 homeodomain-containing homolog

homeobox protein CHX10

ocular retardation

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Vsx2 NCBI NCBI:338917