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150572 SMYD1

150572

SMYD1

SET and MYND domain containing 1

protein-coding

Homo sapiens

基因描述

Type Description
Definition SET and MYND domain containing 1

研究结论

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

名称对应

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

全选

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