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79730 NSUN7

79730

NSUN7

NOP2/Sun RNA methyltransferase family member 7

protein-coding

Homo sapiens

基因描述

Type Description
Definition NOP2/Sun RNA methyltransferase family member 7

研究结论

Date Results Publications
2017-04-08 11:30:00 mutant protein structures of Nsun7 indicated that the amino acid serine was converted to alanine, the structure of the helix, coil and strand was changed, and the protein folding and ligand binding sites were changed in samples from asthenospermic men with a transversion mutation in exon 7, indicating impairment of protein function. Because Nsun7 plays a role in sperm motility, mutation in exon 7 may lead to infertility. 24384068
2016-06-11 11:44:00 Our findings revealed that genetic polymorphisms in exon7 of the NSUN7 gene are not associated with asthenospermia in Chinese Han men. 26345859
2016-03-19 12:14:00 Nsun7 (A11337)-deletion mutation, causes reduction of its protein rate and associated with sperm motility defect in infertile men. 25702163

名称对应

Type IDs
Gene
UniProtKB-ID: NSUN7_HUMAN
UniprotKB: Q8NE18
UniParc: UPI000066D9E8, UPI000013C8AD, UPI00001AE65E
EMBL: AK024063, AK094298, AC131953, BC036568
Ensembl: ENSG00000179299
KO: hsa:79730
Nucleutide sequences
EMBL-CDS: AAH36568.1, BAC04325.1, BAB14808.1
Ensembl_TRS: ENST00000381782, ENST00000316607
Protein sequencees
Ensembl_PRO: ENSP00000371201, ENSP00000319127
RefSeq: XP_016864102.1, NP_078953.4, NP_001317577.1, XP_016864101.1, XP_016864100.1, XP_016864104.1
Others
UniRef100: UniRef100_Q8NE18
UniRef90: UniRef90_Q8NE18
UniRef50: UniRef50_Q14AW5
UniGene: Hs.570821
CCDS: CCDS82917.1, CCDS3461.2

全选

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