| Type | Description |
|---|---|
| Definition | claudin 16 |
| Date | Results | Publications |
|---|---|---|
| 2020-02-01 11:37:00 | To gain more understanding about the mechanisms by which CLDN16 mutations can induce FHHNC, we performed an in-depth computational analysis of the CLDN16 gene and protein, focusing specifically on the prediction of the latter's subcellular localization. | 31357502 |
| 2019-12-21 11:23:00 | No significant associations were found among claudin-16 and claudin-19 single-nucleotide polymorphisms and calcium excretion and between claudin-14, claudin-16, and claudin-19 single-nucleotide polymorphisms and stones. | 30232134 |
| 2019-10-12 10:57:00 | This study demonstrated that a female-specific role clnd16 in tau pathology | 29967939 |
| 2019-08-24 10:10:00 | Mutations in CLDN16 that encodes claudin-16, a tight-junction protein involved in paracellular reabsorption of magnesium and calcium in the renal tubule. | 30621608 |
| 2019-02-09 11:10:00 | Results show that CLDN16 mutation c.602G>A had no effect on pre-mRNA splicing in familial hypomagnesemia with hypercalciuria and nephrocalcinosis. This study expands the genotypic classification of this rare disease and provides the first report of a CLDN19 mutation affecting splicing. | 30576809 |
| Type | IDs |
|---|---|
| Synonymous | HOMG3, PCLN1 |
| Gene |
UniProtKB-ID:
CLD16_HUMAN
UniprotKB:
Q9Y5I7
UniParc:
UPI0000127AB8
EMBL:
AF152101,
BC069777,
BC069662,
BC069759,
BC069682
Ensembl:
ENSG00000113946
KO:
hsa:10686
|
| Nucleutide sequences |
EMBL-CDS:
AAH69759.1,
AAH69682.1,
AAH69662.1,
AAD43096.1,
AAH69777.1
Ensembl_TRS:
ENST00000264734
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000264734
RefSeq:
NP_001365421.1,
NP_001365422.1,
NP_006571.2
|
| Others |
UniRef100:
UniRef100_Q9Y5I7
UniRef90:
UniRef90_Q9Y5I7
UniRef50:
UniRef50_Q9Y5I7
UniGene:
Hs.251391
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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