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65109 UPF3B

65109

UPF3B

UPF3B regulator of nonsense mediated mRNA decay

protein-coding

Homo sapiens

基因描述

Type Description
Definition UPF3B regulator of nonsense mediated mRNA decay

研究结论

Date Results Publications
2019-07-06 10:50:00 RNAseq studies reveal that depletion of ICE1 globally enhances accumulation and stability of NMD-target mRNAs. Further, our data suggest that ICE1 uses a putative MIF4G domain to interact with exon junction complex (EJC) proteins and promotes the association of the NMD protein UPF3B with the EJC. 29528287
2017-10-21 12:24:00 The authors discovered that UPF3B (i) interacts with the release factors, (ii) delays translation termination and (iii) dissociates post-termination ribosomal complexes that are devoid of the nascent peptide. 28899899
2016-10-22 11:57:00 UPF3B gene mutation is associated with Lujan-Fryns syndrome. 26358559
2016-01-23 11:02:00 the neurodevelopmental phenotype of UPF3B missense mutation is caused by impairment of nonsense-mediated mRNA decay pathway function altering neuronal differentiation. 26012578
2014-01-25 11:10:00 These findings indicate that SATB2 activates UPF3B expression through binding to its promoter. 23925499

名称对应

Type IDs
Synonymous HUPF3B, MRX62, MRXS14, RENT3B, UPF3BP1, UPF3BP2, UPF3BP3, UPF3X, Upf3p-X
Gene
UniProtKB-ID: REN3B_HUMAN
UniprotKB: Q9BZI7
UniParc: UPI000006FF6A, UPI000006D21C
EMBL: AF318576, CH471161, AY013251, BC121017
Ensembl: ENSG00000125351
KO: hsa:65109
Nucleutide sequences
EMBL-CDS: EAW89845.1, AAI21018.1, AAG48511.1, EAW89842.1, EAW89844.1, EAW89846.1, AAG60691.1
Ensembl_TRS: ENST00000345865, ENST00000276201
Protein sequencees
Ensembl_PRO: ENSP00000245418, ENSP00000276201
RefSeq: NP_075386.1, XP_016885226.1, XP_016885229.1, XP_016885227.1, XP_016885228.1, NP_542199.1
Others
UniRef100: UniRef100_Q9BZI7
UniRef90: UniRef90_Q9BZI7
UniRef50: UniRef50_Q9BZI7
UniGene: Hs.103832
CCDS: CCDS14588.1, CCDS14587.1

全选

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