Type | Description |
---|---|
Definition | solute carrier family 52 member 3 |
Date | Results | Publications |
---|---|---|
2021-04-03 13:37:00 | An Association and Meta-Analysis of Esophageal Squamous Cell Carcinoma Risk Associated with PLCE1 rs2274223, C20orf54 rs13042395 and RUNX1 rs2014300 Polymorphisms. | 30666517 |
2020-08-01 13:20:00 | Reports on 109 patients with a genetically confirmed diagnosis of riboflavin transporter deficiency are summarized in order to highlight commonly presenting clinical features and possible differences between patients with pathogenic SLC52A2 (RTD2) or SLC52A3 (RTD3) mutations. [review] | 30793323 |
2019-07-13 11:11:00 | Justification for screening SLC52A3 included notable clinical similarities between Brown-Vialetto-Van Laere syndrome | 30553531 |
2019-07-06 10:03:00 | In the in vitro model, exposing Caco-2 cells to tumor necrosis factor-alpha (TNF-alpha) led to a significant inhibition in RF uptake, an effect that was abrogated upon knocking down TNF receptor 1 (TNFR1). The inhibition in RF uptake was associated with a significant reduction in the expression of hRFVT-3 and -1 protein and mRNA levels, as well as in the activity of the SLC52A3 and SLC52A1 promoters | 30156861 |
2018-11-03 11:27:00 | The riboflavin transporter-3 (SLC52A3) 5'-flanking regions contain NF-kappaB p65/Rel-B-binding sites, which are crucial for mediating SLC52A3 transcriptional activity in esophageal squamous cell carcinoma (ESCC) cells. | 29428966 |
Type | IDs |
---|---|
Synonymous | BVVLS, BVVLS1, C20orf54, RFT2, RFVT3, bA371L19.1, hRFT2 |
Gene |
UniProtKB-ID:
S52A3_HUMAN
UniprotKB:
Q9NQ40
UniParc:
UPI000002A74E,
UPI000002A74D
EMBL:
AK291706,
AK074650,
JX478249,
BC009750,
KY978479,
AL118502,
KY978478,
CH471133
Ensembl:
ENSG00000101276
KO:
hsa:113278
|
Nucleutide sequences |
EMBL-CDS:
AUI80409.1,
EAX10658.1,
BAF84395.1,
AAH09750.2,
EAX10659.1,
AFS68799.1,
AUI80410.1,
BAC11113.1
Ensembl_TRS:
ENST00000645534,
ENST00000381944,
ENST00000217254,
ENST00000488495
|
Protein sequencees |
Ensembl_PRO:
ENSP00000494009,
ENSP00000371370,
ENSP00000494193,
ENSP00000217254
RefSeq:
NP_001357015.1,
NP_212134.3,
NP_001357014.1,
XP_024307589.1
|
Others |
UniRef100:
UniRef100_Q9NQ40
UniRef90:
UniRef90_Q9NQ40
UniRef50:
UniRef50_Q9NQ40
UniGene:
Hs.283865
CCDS:
CCDS13007.1
|
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