1. Gene
  2. Snta1 - syntrophin, alpha 1 Gene

Snta1 - syntrophin, alpha 1 Gene

种属: Rattus norvegicus

基因 ID: 362242 | 基因类型: protein coding

关于 Snta1

功能概要

Enables PDZ domain binding activity. Predicted to be involved in several processes, including negative regulation of peptidyl-cysteine S-nitrosylation; regulation of ion transmembrane transport; and ventricular cardiac muscle cell action potential. Predicted to act upstream of or within neuromuscular junction development and regulation of vasoconstriction by circulating norepinephrine. Located in neuromuscular junction and sarcolemma. Biomarker of status epilepticus. Human ortholog(s) of this gene implicated in long QT syndrome; long QT syndrome 12; and sudden infant death syndrome. Orthologous to human SNTA1 (syntrophin alpha 1). [provided by Alliance of Genome Resources, Apr 2022]

Snta1 基因产物(1)

mRNA Protein Name
NM_001100901.1 NP_001094371.1 alpha-1-syntrophin
基因本体论
  • 分子功能
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables PDZ domain binding IPI
IPI: 通过物理相互作用推断
15024025 RGD
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in neuromuscular junction IDA
IDA: 通过直接分析推断
7819523 RGD
located in sarcolemma IDA
IDA: 通过直接分析推断
7819523 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

alpha-1-syntrophin

syntrophin, acidic 1

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Snta1 NCBI NCBI:6640