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90007 MIDN

90007

MIDN

midnolin

protein-coding

Homo sapiens

基因描述

Type Description
Definition midnolin

研究结论

Date Results Publications
2020-09-26 13:02:00 Midnolin is a confirmed genetic risk factor for Parkinson's disease. 31588691
2019-02-09 12:00:00 MIDN promotes the expression of parkin E3 ubiquitin ligase, and that MIDN loss can trigger Parkinson's disease-related pathogenic mechanisms. 28724963
2014-02-15 10:10:00 midnolin plays a role in cellular signaling of adult tissues and regulates glucokinase enzyme activity in pancreatic beta cells 24187134

名称对应

Type IDs
Gene
UniProtKB-ID: MIDN_HUMAN
UniprotKB: Q504T8
UniParc: UPI0000202EF1
EMBL: BC015089, BC094778
Ensembl: ENSG00000167470
KO: hsa:90007
Nucleutide sequences
EMBL-CDS: AAH94778.1, AAH15089.2
Ensembl_TRS: ENST00000300952, ENST00000591446
Protein sequencees
Ensembl_PRO: ENSP00000467679, ENSP00000300952
RefSeq: XP_024307522.1, NP_001375236.1, NP_001375235.1, NP_001375403.1, XP_024307521.1, NP_796375.3, XP_005259729.1
Others
UniRef100: UniRef100_Q504T8
UniRef90: UniRef90_Q504T8
UniRef50: UniRef50_Q3TPJ7
UniGene: Hs.465529
CCDS: CCDS32864.1

全选

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研究热度

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