1. Gene
  2. Nsun5 - NOL1/NOP2/Sun domain family, member 5 Gene

Nsun5 - NOL1/NOP2/Sun domain family, member 5 Gene

种属: Mus musculus

同用名: Nol1r; Wbscr20; Wbscr20a; 9830109N13Rik

基因 ID: 100609 | 基因类型: protein coding

关于 Nsun5

功能概要

Enables rRNA (cytosine-C5-)-methyltransferase activity. Involved in several processes, including central nervous system development; rRNA base methylation; and regulation of myelination. Predicted to be located in nucleoplasm. Predicted to be active in nucleolus. Is expressed in several structures, including alimentary system; branchial arch; central nervous system; genitourinary system; and sensory organ. Orthologous to several human genes including NSUN5 (NOP2/Sun RNA methyltransferase 5). [provided by Alliance of Genome Resources, Apr 2022]

Nsun5 基因产物(2)

mRNA Protein Name
NM_001359617.1 NP_001346546.1 28S rRNA (cytosine-C(5))-methyltransferase isoform 2
NM_145414.2 NP_663389.2 28S rRNA (cytosine-C(5))-methyltransferase isoform 1
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables rRNA (cytosine-C5-)-methyltransferase activity IDA
IDA: 通过直接分析推断
31722427 MGI
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cerebral cortex development IMP
IMP: 通过突变表型推断
31462248 MGI
involved in cognition IMP
IMP: 通过突变表型推断
30485550 MGI
involved in corpus callosum development IMP
IMP: 通过突变表型推断
31174389 MGI
involved in oligodendrocyte development IMP
IMP: 通过突变表型推断
30485550 MGI
involved in rRNA base methylation IDA
IDA: 通过直接分析推断
31722427 MGI
involved in regulation of myelination IMP
IMP: 通过突变表型推断
31174389 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

28S rRNA (cytosine-C(5))-methyltransferase

Williams Beuren syndrome chromosome region 20A homolog

Williams-Beuren syndrome critical region protein 20

probable 28S rRNA (cytosine-C(5))-methyltransferase

putative methyltransferase NSUN5

williams-Beuren syndrome chromosomal region 20A protein hom

直系同源

种属 基因名 来源 基因 ID
Homo sapiens Nsun5 NCBI NCBI:55695