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55867 SLC22A11

55867

SLC22A11

solute carrier family 22 member 11

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 22 member 11

研究结论

Date Results Publications
2020-06-27 11:53:00 our study discovered 3 novel population-specific functional genetic variants (rs6913677, rs2078267, rs8100011) in 2 novel (SLC22A11 and ZNF45) and 1 earlier reported gene (BAI3) for BMI in Indians. Our study decodes key genomic loci underlying obesity phenotype in Indians that may serve as prospective drug targets in future 32363570
2016-12-24 10:13:00 The first genome-wide association study for serum uric acid level in Indians revealed association of SLC2A9, SLC22A11 and ABCG2 gene variants at genome wide significance level in Type 2 diabetes patients. 26902266
2016-08-27 10:59:00 modifies placental passage of perfluorinated alkyl acids, may decrease fetal exposure 26303760
2016-07-02 10:20:00 The regulation of hOAT4 activity was mediated by sgk2 acting through Nedd4-2. 26740304
2015-08-29 10:19:00 SLC22A11 at the basal plasma membrane of human placental syncytiotrophoblasts plays a predominant role in the uptake of 16alpha-OH DHEAS for placental estriol synthesis. 25919187

名称对应

Type IDs
Synonymous OAT4, hOAT4
Gene
UniProtKB-ID: S22AB_HUMAN
UniprotKB: Q9NSA0
UniParc: UPI00001C1114, UPI000003ED3F
EMBL: AK129930, AK075224, BC034384, CH471076, AK222869, AC044790, AB026116, AK290791
Ensembl: ENSG00000168065
KO: hsa:55867
Nucleutide sequences
EMBL-CDS: BAA95316.1, BAF83480.1, EAW74269.1, AAK68155.1, BAC85252.1, AAH34384.1, BAD96589.1, BAC11483.1
Ensembl_TRS: ENST00000301891, ENST00000377585
Protein sequencees
Ensembl_PRO: ENSP00000301891, ENSP00000366809
RefSeq: NP_060954.1, XP_011543469.1, NP_001294914.1
Others
UniRef100: UniRef100_Q9NSA0
UniRef90: UniRef90_Q9NSA0
UniRef50: UniRef50_Q9NSA0
UniGene: Hs.220844
CCDS: CCDS8074.1, CCDS76425.1

全选

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