Type | Description |
---|---|
Definition | synaptotagmin 9 |
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 |
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
|
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Refseq |
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