Type | Description |
---|---|
Definition | solute carrier protein family 52, member 3 |
Date | Results | Publications |
---|---|---|
2021-02-20 13:31:00 | Effect of riboflavin deficiency on development of the cerebral cortex in Slc52a3 knockout mice. | 33116204 |
2018-04-28 11:58:00 | our knowledge, this is the first report to indicate that Rfvt3 contributes to placental riboflavin transport, and that disruption of Slc52a3 gene caused neonatal mortality with hyperlipidemia and hypoglycemia owing to riboflavin deficiency. | 27272163 |
2017-08-19 11:01:00 | Loss of Slc52a3 gene is associated with Brown-Vialetto-van Laere syndrome. | 26976849 |
2016-07-02 11:44:00 | the RFVT-3 system is the main transporter involved in carrier-mediated riboflavin uptake in the native mouse small and large intestine | 26660539 |
Type | IDs |
---|---|
Synonymous | 2310046K01Rik, RFT2 |
Gene |
UniProtKB-ID:
S52A3_MOUSE
UniprotKB:
Q9D6X5
UniParc:
UPI0000025283,
UPI0000022BE5
EMBL:
AK154970,
CH466551,
AK029091,
BC016127,
AK170158,
AL845161,
AK009850
Ensembl:
ENSMUSG00000027463
KO:
mmu:69698
|
Nucleutide sequences |
EMBL-CDS:
AAH16127.1,
BAC26290.1,
BAE41605.1,
BAB26542.1,
EDL05945.1,
BAE32962.1
Ensembl_TRS:
ENSMUST00000073228,
ENSMUST00000109858,
ENSMUST00000109861,
ENSMUST00000109859
|
Protein sequencees |
Ensembl_PRO:
ENSMUSP00000105484,
ENSMUSP00000072961,
ENSMUSP00000105485,
ENSMUSP00000105487
RefSeq:
NP_001158292.1,
NP_001158291.1,
NP_081448.2
|
Others |
UniRef100:
UniRef100_Q9D6X5
UniRef90:
UniRef90_Q9D6X5
UniRef50:
UniRef50_Q9D6X5
UniGene:
Mm.258262
CCDS:
CCDS50749.1,
CCDS16876.1
|
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Refseq |
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