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254428 SLC41A1

254428

SLC41A1

solute carrier family 41 member 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 41 member 1

研究结论

Date Results Publications
2017-11-11 12:49:00 Knockdown of SLC41A1 magnesium transporter promotes mineralization and attenuates magnesium inhibition during osteogenesis of mesenchymal stromal cells. 28222767
2017-03-11 11:41:00 The association of rs11240569 polymorphism in SLC41A1 gene with reduced risk of Parkinson's Disease was replicated in our population. 27612022
2016-09-10 11:31:00 Authors performed direct DNA sequencing of the SLC41A1 gene in 100 early-onset PD cases. 26308152
2016-02-13 12:49:00 Na+-dependent Mg2+ efflux conducted by Na+/Mg2+ exchanger SLC41A1 is regulated by insulin. 26355001
2015-01-17 11:53:00 This study has shown loss of Mg(2+) efflux function consequent to SLC41A1 R244H variant and SLC41A1 coding variants seem to be rare in Taiwanese Parkinson disease. 24661466

名称对应

Type IDs
Synonymous MgtE
Gene
UniProtKB-ID: S41A1_HUMAN, B2RMP2_HUMAN
UniprotKB: Q8IVJ1, B2RMP2
UniParc: UPI000013E1E6
EMBL: BX641054, AJ514402, AL832362, BC136303, AL831974, BX648979, CH471067, AL832001, AK128069
Ensembl: ENSG00000133065
KO: hsa:254428
Nucleutide sequences
EMBL-CDS: CAH56213.1, CAH56217.1, CAH56211.1, CAE46028.1, CAH56135.1, CAD58404.1, BAG54625.1, AAI36304.1, EAW91583.1, EAW91582.1
Gene_ORFName: hCG_19155
Ensembl_TRS: ENST00000367137
Protein sequencees
Ensembl_PRO: ENSP00000356105
RefSeq: NP_776253.3, XP_005245126.1
Others
UniRef100: UniRef100_Q8IVJ1
UniRef90: UniRef90_Q8IVJ1
UniRef50: UniRef50_Q8IVJ1
UniGene: Hs.20274
CCDS: CCDS30988.1

全选

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研究热度

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