Type | Description |
---|---|
Definition | SET and MYND domain containing 1 |
Date | Results | Publications |
---|---|---|
2021-04-17 13:13:00 | Stability of Smyd1 in endothelial cells is controlled by PML-dependent SUMOylation upon cytokine stimulation. | 33241844 |
2020-10-24 14:05:00 | Modulation of chromatin remodeling proteins SMYD1 and SMARCD1 promotes contractile function of human pluripotent stem cell-derived ventricular cardiomyocyte in 3D-engineered cardiac tissues. | 31097748 |
2019-11-23 12:48:00 | This novel mutation (c.814T>C/p.F272L) may be the first identified disease-causing mutation of SMYD1 in Hypertrophic cardiomyopathy (HCM) patients worldwide. | 30205637 |
2018-12-29 11:28:00 | We present genetic and statistical evidence that the R320Q substitution in SMYD1 underlies an inherited form of the AnWj-negative blood group phenotype. The mechanism by which the mutation leads to this phenotype remains to be determined. | 29956848 |
2016-07-30 10:47:00 | SMYD1 serves as an Serum Response Factor-interacting protein, enhances Serum Response Factor DNA binding activity, and is required for endothelial cell migration and tube formation to regulate angiogenesis. | 26799706 |
Type | IDs |
---|---|
Synonymous | BOP, KMT3D, ZMYND18, ZMYND22 |
Gene |
UniProtKB-ID:
SMYD1_HUMAN,
Q5HYE8_HUMAN,
E9PHG3_HUMAN
UniprotKB:
Q8NB12,
Q5HYE8,
E9PHG3
UniParc:
UPI000198C5D4,
UPI000006EB68,
UPI00004C414E
EMBL:
AL832035,
AC092836,
AK091724,
BC126191,
BX647878
Ensembl:
ENSG00000115593
KO:
hsa:150572
|
Nucleutide sequences |
EMBL-CDS:
CAI46139.1,
BAC03732.1,
AAI26192.1,
CAI46077.1
Ensembl_TRS:
ENST00000419482,
ENST00000444564
|
Protein sequencees |
Ensembl_PRO:
ENSP00000393453,
ENSP00000407888
RefSeq:
NP_001317293.1,
NP_938015.1
|
Others |
UniRef100:
UniRef100_Q8NB12,
UniRef100_E9PHG3,
UniRef100_Q5HYE8
UniRef90:
UniRef90_E9PHG3,
UniRef90_Q8NB12
UniRef50:
UniRef50_Q8NB12,
UniRef50_Q2MJQ9
UniGene:
Hs.516176
CCDS:
CCDS33240.1
|
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Refseq |
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