| Type | Description |
|---|---|
| Definition | barttin CLCNK type accessory beta subunit |
| Date | Results | Publications |
|---|---|---|
| 2020-04-18 11:43:00 | Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome. | 31879347 |
| 2018-08-18 10:41:00 | our study provides in vivo evidence that, in response to a low-potassium diet, ClC-K and barttin play important roles in the activation of the cascade and blood pressure regulation. | 29326302 |
| 2010-01-21 00:00:00 | Bsnd(-/-) mice thus demonstrate a novel function of Cl(-) channels in generating the endocochlear potential and reveal the mechanism leading to deafness in human Bartter syndrome IV. | 18833191 |
| 2010-01-21 00:00:00 | induction of SGK1, CLC-K1 and barttin by high osmolarity and change in intracellular volume in distal renal tubular cells in vivo and in vitro | 18614997 |
| Type | IDs |
|---|---|
| Gene |
UniProtKB-ID:
BSND_MOUSE
UniprotKB:
Q8VIM4
UniParc:
UPI000002260B
EMBL:
AL954352,
BC038287,
AY373833,
AF391088,
AK052587
Ensembl:
ENSMUSG00000025418
KO:
mmu:140475
|
| Nucleutide sequences |
EMBL-CDS:
AAQ81629.1,
BAC35049.1,
AAH38287.1,
AAL33907.1
Ensembl_TRS:
ENSMUST00000054472
|
| Protein sequencees |
Ensembl_PRO:
ENSMUSP00000049563
RefSeq:
NP_536706.2
|
| Others |
UniRef100:
UniRef100_Q8VIM4
UniRef90:
UniRef90_Q8VIM4
UniRef50:
UniRef50_Q8WZ55
UniGene:
Mm.135448
CCDS:
CCDS18419.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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| Conserved domain | Region: {{conservedDomain.region == '' || conservedDomain.region == null ? "-": conservedDomain.region}} GFID: {{conservedDomain.gfid == '' || conservedDomain.gfid == null ? "-": conservedDomain.gfid}} Family: {{conservedDomain.family == '' || conservedDomain.family == null ? "-": conservedDomain.family}} CDD: {{conservedDomain.cdd}} - |
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