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13521 Slc26a2

13521

Slc26a2

solute carrier family 26 (sulfate transporter), member 2

protein-coding

Mus musculus

基因描述

Type Description
Definition solute carrier family 26 (sulfate transporter), member 2

研究结论

Date Results Publications
2020-07-11 11:39:00 support a multifactorial etiology, involving congenitally predisposed isthmic conditions, altered biomechanics, and age-dependent bone loss, which leads to SLC26A2-related spondylolysis 31914611
2019-06-29 11:16:00 the present study has expanded our view of the sulfate transporter SLC26A2 to the unexpected field of collagen secretion and proteostasis. Our findings will facilitate the understanding of genotype-phenotype relationships of SLC26A2-related chondrodysplasias and accelerate the development of drug therapy against ACG1B and AO2. 30685387
2014-09-13 12:14:00 Diastrophic dysplasia sulfate transporter (SLC26A2) is expressed in the adrenal cortex and regulates aldosterone secretion. 24591336
2014-03-29 10:05:00 These findings reveal multiple roles for Slc26a2 in chondrocyte biology and emphasize the importance of Slc26a2-mediated protein sulfation in cell signaling 24302720
2012-09-22 10:50:00 a Slc26a2 mutation results in matrix disruptions, growth, and degradation of cartilage with impaired sulfation 22556422

名称对应

Type IDs
Synonymous Dtd, ST-OB
Gene
UniProtKB-ID: S26A2_MOUSE
UniprotKB: Q62273
UniParc: UPI00000040D2
EMBL: AK163974, CH466528, D42049, BC028345, AK052942
Ensembl: ENSMUSG00000034320
KO: mmu:13521
Nucleutide sequences
EMBL-CDS: EDL09779.1, BAE37562.1, BAC35214.1, BAA07650.1, AAH28345.1
Ensembl_TRS: ENSMUST00000146409
Protein sequencees
Ensembl_PRO: ENSMUSP00000119447
RefSeq: NP_031911.1
Others
UniRef100: UniRef100_Q62273
UniRef90: UniRef90_O70531
UniRef50: UniRef50_P50443
UniGene: Mm.24803
CCDS: CCDS29282.1

全选

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研究热度

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