Type | Description |
---|---|
Definition | solute carrier family 18 member A1 |
Date | Results | Publications |
---|---|---|
2020-02-01 13:34:00 | Finding suggests that monoamine uptake by VMAT1 initially declined in early human evolution (from 130Glu/136Asn to 130Gly/136Thr) but increased along with the emergence of the 130Gly/136Ile variant around the time of the out of Africa dispersal of modern humans. | 31791232 |
2020-01-25 14:25:00 | SV2 was highly expressed in neuroblastoma (NB) and can thus be useful marker in NB diagnostics. VMAT1 and VMAT2 were also expressed in NB but similar to syn less reliable as tumor markers. | 31317476 |
2019-08-17 12:23:00 | SLC18A1 variants correlated with Anger and Vigor scores, only among males. | 30656852 |
2019-05-04 12:42:00 | SLC18A1 as one potential pleiotropic gene overlapped between Mood disorders and Cardiometabolic diseases. Genetic variation in SLC18A1 made statistically significant contributions to Body Mass Index. | 29998543 |
2018-12-01 10:05:00 | SLC18A1 might complement other biomarkers currently under study in relation to programmed cell death protein 1/programmed cell death protein ligand 1 inhibition | 30194079 |
Type | IDs |
---|---|
Synonymous | CGAT, VAT1, VMAT1 |
Gene |
UniProtKB-ID:
VMAT1_HUMAN,
Q96GL6_HUMAN
UniprotKB:
P54219,
Q96GL6
UniParc:
UPI00001389CE,
UPI000186C999,
UPI000006FF6B,
UPI000013D686
EMBL:
AC025853,
BC009387,
U39905,
BC006317
Ensembl:
ENSG00000036565
KO:
hsa:6570
|
Nucleutide sequences |
EMBL-CDS:
AAH06317.1,
AAC50472.1,
AAH09387.1
Ensembl_TRS:
ENST00000265808,
ENST00000381608,
ENST00000440926,
ENST00000519026,
ENST00000276373,
ENST00000437980,
ENST00000517776
|
Protein sequencees |
Ensembl_PRO:
ENSP00000265808,
ENSP00000429664,
ENSP00000276373,
ENSP00000413361,
ENSP00000387549,
ENSP00000371021,
ENSP00000428001
RefSeq:
NP_001135797.1,
XP_011542927.1,
NP_003044.1,
NP_001129163.1,
NP_001135796.1,
XP_011542928.1
|
Others |
UniRef100:
UniRef100_P54219,
UniRef100_Q96GL6
UniRef90:
UniRef90_P54219,
UniRef90_Q96GL6
UniRef50:
UniRef50_P54219,
UniRef50_A0A3Q3BG18
UniGene:
Hs.158322
CCDS:
CCDS6013.1,
CCDS47814.1,
CCDS47815.1
|
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