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157570 ESCO2

157570

ESCO2

establishment of sister chromatid cohesion N-acetyltransferase 2

protein-coding

Homo sapiens

基因描述

Type Description
Definition establishment of sister chromatid cohesion N-acetyltransferase 2

研究结论

Date Results Publications
2021-01-09 13:33:00 Juberg-Hayward syndrome and Roberts syndrome are allelic, caused by mutations in ESCO2. 32977150
2020-12-12 13:22:00 Alternative catalytic residues in the active site of Esco acetyltransferases. 32555289
2020-10-31 13:14:00 The role of ESCO2, SALL4 and TBX5 genes in the susceptibility to thalidomide teratogenesis. 31388035
2020-04-04 10:31:00 DDX11, ESCO1 and ESCO2 control different fractions of cohesin that are spatially and mechanistically separated. 31935221
2019-10-19 11:04:00 MCM complex couples ESCO2 with DNA replication and that the CUL4-DDB1-VPRBP complex promotes post-replicative ESCO2 degradation, presumably to suppress cohesion formation during mitosis. 30100344

名称对应

Type IDs
Synonymous 2410004I17Rik, EFO2, EFO2p, RBS, hEFO2
Gene
UniProtKB-ID: ESCO2_HUMAN
UniprotKB: Q56NI9
UniParc: UPI000056F154, UPI0000160D17
EMBL: AK124215, AY882862, AC104997, BC034641
Ensembl: ENSG00000171320
KO: hsa:157570
Nucleutide sequences
EMBL-CDS: AAX68677.1, AAH34641.1, BAG54021.1
Ensembl_TRS: ENST00000397418, ENST00000305188
Protein sequencees
Ensembl_PRO: ENSP00000380563, ENSP00000306999
RefSeq: XP_011542724.1, NP_001017420.1, XP_011542723.1
Others
UniRef100: UniRef100_Q56NI9
UniRef90: UniRef90_Q56NI9
UniRef50: UniRef50_Q56NI9
UniGene: Hs.99480
CCDS: CCDS34872.1

全选

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