| Type | Description |
|---|---|
| Definition | solute carrier family 9 member A3 |
| Date | Results | Publications |
|---|---|---|
| 2021-02-06 13:55:00 | Altered absorptive function in the gall bladder during cholesterol gallstone formation is associated with abnormal NHE3 complex formation. | 32557227 |
| 2020-05-02 12:28:00 | Most of Taiwanese congenital bilateral absence of vas deferens (CBAVD) have at least one variant of SLC9A3 deletion and CFTR IVS8-5T, which co-contribute to Taiwanese CBAVD. [review] | 30797621 |
| 2020-02-15 10:46:00 | The knowledge of this genetic form of non-syndromic CSD means that it can be detected early during the third trimester of pregnancy by the combined use of US signs, MRI and amniotic fluid digestive enzymes. Its main differential diagnosis is CCD due to mutation of the SLC26A3 gene. | 31276831 |
| 2019-08-17 11:38:00 | Low NHE3 expression is associated with hypophosphatemia in calcium stone formers. | 29126251 |
| 2019-07-27 11:00:00 | an association between congenital bilateral absence of the vas deferens (CBAVD) and loss of SLC9A3 and propose that specific defects in the reproductive duct due to SLC9A3 variants drive CBAVD development. | 30956978 |
| Type | IDs |
|---|---|
| Synonymous | DIAR8, NHE-3, NHE3 |
| Gene |
UniProtKB-ID:
SL9A3_HUMAN
UniprotKB:
P48764
UniParc:
UPI0001D3B0BF,
UPI000013D597
EMBL:
BC101669,
U28043,
BC143328,
AC010442,
AC106772,
BC101671
Ensembl:
ENSG00000066230
KO:
hsa:6550
|
| Nucleutide sequences |
EMBL-CDS:
AAI01670.1,
AAB48990.1,
AAI01672.1,
AAI43329.1
Ensembl_TRS:
ENST00000514375,
ENST00000264938
|
| Protein sequencees |
Ensembl_PRO:
ENSP00000264938,
ENSP00000422983
RefSeq:
NP_001271280.1,
NP_004165.2
|
| Others |
UniRef100:
UniRef100_P48764
UniRef90:
UniRef90_P48764
UniRef50:
UniRef50_P26433
UniGene:
Hs.658120
CCDS:
CCDS3855.1,
CCDS64116.1
|
| {{proteinIndex+1}} | mRNA | Protein | UniprotKB | Description | ||||
|---|---|---|---|---|---|---|---|---|
| Refseq |
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