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54716 SLC6A20

54716

SLC6A20

solute carrier family 6 member 20

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 6 member 20

研究结论

Date Results Publications
2021-03-13 13:25:00 Genome and epigenome editing identify CCR9 and SLC6A20 as target genes at the 3p21.31 locus associated with severe COVID-19. 33619245
2020-09-12 16:01:00 Associations of SLC6A20 genetic polymorphisms with Hirschsprung's disease in a Southern Chinese population. 31358688
2020-06-12 10:48:00 Characterization and substrate specificity of the Na+ coupled IMINO transport system in apical brush border membranes of epithelial cells. Identically found in kidney proximal tubule. 3571270
2019-08-17 10:06:00 SIT1 is not expressed in small intestine of human newborns. 30160974
2016-09-24 10:52:00 Imputed meta-analysis revealed that 13 SLC6A20 SNPs were significantly associated with Hirschsprung disease. In further subgroup analysis, SLC6A20 polymorphisms appeared to have increased associations with Long-Segment Hirschsprung disease. 26049783

名称对应

Type IDs
Synonymous SIT1, XT3, Xtrp3
Gene
UniProtKB-ID: S6A20_HUMAN
UniprotKB: Q9NP91
UniParc: UPI000002A162, UPI0000046064
EMBL: AL389979, BC126197, AJ276208, AJ289880, AF125107, CH471055, AJ276207, AF075260, BC136431
Ensembl: ENSG00000163817
KO: hsa:54716
Nucleutide sequences
EMBL-CDS: CAB97535.1, CAB99310.1, CAB99311.1, EAW64748.1, AAC27755.1, CAB96872.1, AAL75944.1, AAI26198.1, AAI36432.1
Ensembl_TRS: ENST00000353278, ENST00000358525
Protein sequencees
Ensembl_PRO: ENSP00000346298, ENSP00000296133
RefSeq: XP_011532150.1, NP_071800.1, XP_011532149.1, NP_064593.1, NP_001372612.1
Others
UniRef100: UniRef100_Q9NP91
UniRef90: UniRef90_Q9NP91
UniRef50: UniRef50_Q9NP91
UniGene: Hs.413095
CCDS: CCDS2730.1, CCDS43077.1

全选

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