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55329 MNS1

55329

MNS1

meiosis specific nuclear structural 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition meiosis specific nuclear structural 1

研究结论

Date Results Publications
2021-02-06 13:48:00 MNS1 variant associated with situs inversus and male infertility. 31534215
2019-01-19 11:02:00 MNS1 deficiency in humans causes laterality defects (situs inversus) and likely male infertility, and that MNS1 plays a role in the outer dynein arm-docking complex assembly. 30148830
2008-10-22 10:03:00 Cloning and functional characterization of a highly similar gene in mouse. 8032679
2008-10-20 14:00:00 A rat homologous protein was among the the nuclear proteins that change in abundance or form in response to prolonged hypoxia in the rat kidney fibroblasts. 15942958

名称对应

Type IDs
Synonymous SPATA40
Gene
UniProtKB-ID: MNS1_HUMAN, B3KQ70_HUMAN
UniprotKB: Q8NEH6, B3KQ70
UniParc: UPI0000EE4FA5, UPI0000070061
EMBL: BC034991, AK057542, CH471082, BC031046, AK002084
Ensembl: ENSG00000138587
KO: hsa:55329
Nucleutide sequences
EMBL-CDS: BAA92077.1, AAH34991.1, AAH31046.1, EAW77501.1, BAG51932.1
Gene_ORFName: hCG_40113
Ensembl_TRS: ENST00000260453
Protein sequencees
Ensembl_PRO: ENSP00000260453
RefSeq: NP_060835.1
Others
UniRef100: UniRef100_Q8NEH6
UniRef90: UniRef90_Q8NEH6
UniRef50: UniRef50_Q8NEH6
UniGene: Hs.444483
CCDS: CCDS10158.1

全选

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研究热度

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