1. Gene
  2. USH2A - Ush2a usherin Gene

USH2A - Ush2a usherin Gene

种属: Rattus norvegicus

同用名: RGD1560269

基因 ID: 289369 | 基因类型: protein coding

关于 USH2A

功能概要

Predicted to enable Collagen binding activity; identical protein binding activity; and Myosin binding activity. Involved in retina development in camera-type eye. Located in stereocilium and synapse. Colocalizes with several cellular components, including neuronal cell body; photoreceptor connecting cilium; and photoreceptor inner segment. Human ortholog(s) of this gene implicated in Usher syndrome (multiple); nonsyndromic deafness; and retinitis pigmentosa (multiple). Orthologous to human USH2A (usherin). [provided by Alliance of Genome Resources, Apr 2022]

USH2A 基因产物(1)

mRNA Protein Name
NM_001302219.1 NP_001289148.1 usherin
基因本体论
  • 生物过程
  • 细胞组分
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in retina development in camera-type eye IEP
IEP: 通过表达模式推断
12160733 RGD
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in neuronal cell body IDA
IDA: 通过直接分析推断
16434480 RGD
located in photoreceptor connecting cilium IDA
IDA: 通过直接分析推断
16434480 RGD
located in photoreceptor inner segment IDA
IDA: 通过直接分析推断
16434480 RGD
located in stereocilium IDA
IDA: 通过直接分析推断
16301216 RGD
located in terminal bouton IDA
IDA: 通过直接分析推断
16434480 RGD
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

usherin

Usher syndrome 2A (autosomal recessive, mild) homolog

Usher syndrome 2A homolog

usher syndrome type IIa protein homolog

usher syndrome type-2A protein homolog

直系同源

种属 基因名 来源 基因 ID
Homo sapiens USH2A NCBI NCBI:7399