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69698 Slc52a3

69698

Slc52a3

solute carrier protein family 52, member 3

protein-coding

Mus musculus

基因描述

Type Description
Definition solute carrier protein family 52, member 3

研究结论

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

名称对应

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

全选

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研究热度

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