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80721 Slc19a3

80721

Slc19a3

solute carrier family 19, member 3

protein-coding

Mus musculus

基因描述

Type Description
Definition solute carrier family 19, member 3

研究结论

Date Results Publications
2017-10-21 10:28:00 showed that acute neurodegeneration caused by thiamine deficiency is preventable in most parts, and prompt high-dose thiamine administration is critical for the treatment of THMD2. However, reduction of thiamine should be performed carefully to prevent recurrence after recovery of the disease 28665968
2012-04-21 12:01:00 both mTHTR-1 and mTHTR-2 are involved in carrier-mediated thiamin uptake by pancreatic acinar cells. 22194418
2010-05-10 11:34:00 THTR-2 is required for normal uptake of thiamin in the intestine and can fulfill normal levels of uptake in conditions associated with THTR-1 dysfunction. 19879271
2010-01-21 00:00:00 Intestinal and renal thiamin uptake are developmentally regulated during early stages of life, mediated through mTHTR-1 and mTHTR-2, and suggest the possible involvement of transcriptional regulatory mechanism(s) in this regulation. 16206251
2010-01-21 00:00:00 Pancreatic beta cells and islets take up thiamine by a regulated THTR1/2-mediated process. 19423748

名称对应

Type IDs
Synonymous A230084E24Rik, AI788884, ThTr2
Gene
UniProtKB-ID: S19A3_MOUSE
UniprotKB: Q99PL8
UniParc: UPI000024E538
EMBL: AF271634, BC109155, BC109154
Ensembl: ENSMUSG00000038496
KO: mmu:80721
Nucleutide sequences
EMBL-CDS: AAG53880.1, AAI09156.1, AAI09155.1
Ensembl_TRS: ENSMUST00000045560, ENSMUST00000164473
Protein sequencees
Ensembl_PRO: ENSMUSP00000126646, ENSMUSP00000041683
RefSeq: XP_036010341.1, XP_006496642.1, XP_036010332.1, XP_011237018.1, NP_085033.2, XP_036010334.1, XP_011237017.1
Others
UniRef100: UniRef100_Q99PL8
UniRef90: UniRef90_Q99PL8
UniRef50: UniRef50_Q99PL8
UniGene: Mm.261542
CCDS: CCDS15101.1

全选

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研究热度

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