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6571 SLC18A2

6571

SLC18A2

solute carrier family 18 member A2

protein-coding

Homo sapiens

基因描述

Type Description
Definition solute carrier family 18 member A2

研究结论

Date Results Publications
2020-04-11 10:52:00 Nominal associations were indicated for 20 variants in six genes including an experiment-wise significant association from the combined effect of three SLC18A2 SNPs (rs363332, rs363334 and rs363338) with heroin dependence (pfinal = 0.047). 30983500
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
2019-12-28 11:44:00 Study shows decreased pallidal vesicular monoamine transporter type 2 availability in Parkinson's disease. Findings showed dopamine terminals in the globus pallidus may be differentially vulnerable in different stages of the disease. 30471418
2018-04-07 11:19:00 single nucleotide polymorphisms (rs363223, rs363226, rs363251, and rs363341interact with assessed cognitive impairment after severe traumatic brain injury 26828714
2018-02-24 11:14:00 This study showed that in Chinese patient population, "GG" of rs363371 in VMAT2 may reduce the risk for ALS. 28477711

名称对应

Type IDs
Synonymous PKDYS2, SVAT, SVMT, VAT2, VMAT2
Gene
UniProtKB-ID: VMAT2_HUMAN
UniprotKB: Q05940
UniParc: UPI0000404AA3, UPI00001389DE
EMBL: L09118, BC108928, AL731557, BC108927, L23205, AL391988, CH471066, L14269, BC030593, AB044401, AK314997, X71354
Ensembl: ENSG00000165646
KO: hsa:6571
Nucleutide sequences
EMBL-CDS: BAB19009.1, AAH30593.1, EAW49429.1, AAA91853.1, EAW49428.1, AAA61290.1, AAI08928.1, AAA59877.1, AAI08929.1, BAG37493.1, CAA50489.1
Ensembl_TRS: ENST00000644641
Protein sequencees
Ensembl_PRO: ENSP00000496339
RefSeq: NP_003045.2
Others
UniRef100: UniRef100_Q05940
UniRef90: UniRef90_Q05940
UniRef50: UniRef50_Q05940
UniGene: Hs.596992
CCDS: CCDS7599.1

全选

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研究热度

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