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6854 SYN2

6854

SYN2

synapsin II

protein-coding

Homo sapiens

基因描述

Type Description
Definition synapsin II

研究结论

Date Results Publications
2019-05-18 10:12:00 Our findings support that ASB16-AS1 and SYN2 may represent two novel functional genes underlying bone mineral density variation 29763751
2017-06-10 11:11:00 These findings contribute to previous work showing dysregulation of Synapsins, particularly SYN2, in mood disorders and improve our understanding of the regulatory mechanisms that precipitate these changes likely leading to the BD or MDD phenotype. 27515700
2015-04-25 11:07:00 Both GABRA6 and Synapsin II polymorphisms are important risk factors for the development of idiopathic generalized epilepsy in a South Indian population. 25088614
2014-08-09 12:26:00 Results identify SYN2 as a novel predisposing gene for autism spectrum disorders (ASD) and strengthen the hypothesis that a disturbance of synaptic homeostasis underlies ASD. 23956174
2012-09-01 11:02:00 Synapsin II is involved in the molecular pathway of lithium treatment in bipolar disorder 22384280

名称对应

Type IDs
Synonymous SYNII
Gene
UniProtKB-ID: SYN2_HUMAN, Q86VA8_HUMAN, B3KRB3_HUMAN, Q59GM1_HUMAN
UniprotKB: Q92777, Q86VA8, B3KRB3, Q59GM1
UniParc: UPI000178DFB5, UPI00001969B2, UPI00004F6B78, UPI0000167B8A, UPI000015FFA8
EMBL: AK091286, AB209088, ABBA01025208, BC051307, AC022234, AC026166, AF077737, AF077671, U40215, AC091492
Ensembl: ENSG00000157152
KO: hsa:6854
Nucleutide sequences
EMBL-CDS: AAC33789.1, AAC50718.1, AAC28368.1, AAH51307.1, BAG52325.1, BAD92325.1
Ensembl_TRS: ENST00000621198, ENST00000620175
Protein sequencees
Ensembl_PRO: ENSP00000484916, ENSP00000480050
RefSeq: XP_006713374.1, XP_016862576.1, NP_598328.1, NP_003169.2, XP_006713375.1, XP_006713376.1
Others
UniRef100: UniRef100_A0A5F7ZV61, UniRef100_Q86VA8, UniRef100_Q92777
UniRef90: UniRef90_Q64332, UniRef90_A0A2J8M1E2
UniRef50: UniRef50_Q64332
UniGene: Hs.445503
CCDS: CCDS74901.1, CCDS74900.1

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