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143425 SYT9

143425

SYT9

synaptotagmin 9

protein-coding

Homo sapiens

基因描述

Type Description
Definition synaptotagmin 9

研究结论

Date Results Publications
2018-06-30 12:35:00 The intronic SYT9 variant rs11041321, which exhibits a significant genome-wide association with circulating homocysteine, was associated with the occurrence of congenital cardiac septal defects (CCSDs). This finding helps to characterize the unexpected role of SYT9 in homocysteine metabolism and the development of CCSDs, which further highlighted the interplay of diet, genetics, and human birth defects 28834160
2017-03-22 10:11:00 SYT9 expression is significantly downregulated in human masticatory mucosa during wound healing 28005267
2010-06-30 22:06:00 Clinical trial of gene-disease association and gene-environment interaction. (HuGE Navigator) 20379614

名称对应

Type IDs
Gene
UniProtKB-ID: SYT9_HUMAN
UniprotKB: Q86SS6
UniParc: UPI000000DB7B
EMBL: BC046367
Ensembl: ENSG00000170743
KO: hsa:143425
Nucleutide sequences
EMBL-CDS: AAH46367.1
Ensembl_TRS: ENST00000318881
Protein sequencees
Ensembl_PRO: ENSP00000324419
RefSeq: XP_011518208.1, NP_783860.1, XP_011518202.1, XP_011518206.1, XP_011518203.1, XP_011518204.1, XP_011518209.1
Others
UniRef100: UniRef100_Q86SS6
UniRef90: UniRef90_Q9R0N9
UniRef50: UniRef50_Q9R0N9
UniGene: Hs.177193
CCDS: CCDS7778.1

全选

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研究热度

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