1. Gene
  2. Twnk - twinkle mtDNA helicase Gene

Twnk - twinkle mtDNA helicase Gene

种属: Rattus norvegicus

同用名: Peo1

基因 ID: 309441 | 基因类型: protein coding

关于 Twnk

功能概要

Predicted to enable several functions, including 5'-3' DNA helicase activity; identical protein binding activity; and protease binding activity. Involved in cellular response to glucose stimulus. Located in mitochondrion. Human ortholog(s) of this gene implicated in Perrault syndrome; autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3; chronic progressive external ophthalmoplegia; and mitochondrial DNA depletion syndrome 7. Orthologous to human TWNK (twinkle mtDNA helicase). [provided by Alliance of Genome Resources, Apr 2022]

Twnk 基因产物(1)

mRNA Protein Name
NM_001107599.1 NP_001101069.1 twinkle protein, mitochondrial
基因本体论
  • 生物过程
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cellular response to glucose stimulus IEP
IEP: 通过表达模式推断
22743328 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

twinkle protein, mitochondrial

progressive external ophthalmoplegia 1 homolog

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Twnk NCBI NCBI:56652