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