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10560 SLC19A2

10560

SLC19A2

solute carrier family 19 member 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 19 member 2

研究结论

Date Results Publications
2021-04-13 10:09:00 pH-dependent pyridoxine transport by SLC19A2 and SLC19A3: Implications for absorption in acidic microclimates. 33008889
2021-03-20 13:31:00 3'-UTR Polymorphisms of Vitamin B-Related Genes Are Associated with Osteoporosis and Osteoporotic Vertebral Compression Fractures (OVCFs) in Postmenopausal Women. 32498429
2020-12-19 13:39:00 Posttranscriptional regulation of thiamin transporter-1 expression by microRNA-200a-3p in pancreatic acinar cells. 32683950
2020-09-05 13:56:00 TRMA syndrome with a severe phenotype, cerebral infarction, and novel compound heterozygous SLC19A2 mutation: a case report. 31296181
2020-07-11 10:12:00 Besides reporting a novel mutation of the causative gene SLC19A2, we wanted to emphasize this syndrome in the aspect of coexistence of insulin dependent diabetes, transfusion dependent anemia and thrombocytopenia. 31951336

名称对应

Type IDs
Synonymous TC1, THMD1, THT1, THTR1, TRMA
Gene
UniProtKB-ID: S19A2_HUMAN, A0A024R928_HUMAN, A0A024R8Y5_HUMAN
UniprotKB: O60779, A0A024R928, A0A024R8Y5
UniParc: UPI0000036177, UPI000006EF15
EMBL: AF160756, BC018514, AJ238413, AK316465, CH471067, KU178535, AF160812, KU178534, AF160186, AF158233, AK304021, AL021068, AF272359, AF135488, AF153330, AK313779, AJ237724
Ensembl: ENSG00000117479
KO: hsa:10560
Nucleutide sequences
EMBL-CDS: CAB50770.1, AAD51283.1, AAD54242.1, AAH18514.1, EAW90846.1, AAK54468.1, AAD45985.1, CAB50771.1, BAH14836.1, AAD43534.1, EAW90843.1, BAG64936.1, BAG36517.1, AAF15129.1, AAD51280.1, ALQ33993.1, EAW90845.1, EAW90847.1, ALQ33992.1
Gene_ORFName: hCG_38014, hCG_38014
Ensembl_TRS: ENST00000367804, ENST00000236137
Protein sequencees
Ensembl_PRO: ENSP00000356778, ENSP00000236137
RefSeq: NP_001306596.1, NP_008927.1
Others
UniRef100: UniRef100_O60779, UniRef100_A0A024R8Y5
UniRef90: UniRef90_I3N5R6, UniRef90_O60779
UniRef50: UniRef50_A0A096MJN0, UniRef50_O60779
UniGene: Hs.30246
CCDS: CCDS81398.1, CCDS1280.1

全选

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