Type | Description |
---|---|
Definition | solute carrier family 19 member 2 |
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 |
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
|
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Refseq |
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