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11198 SUPT16H

11198

SUPT16H

SPT16 homolog, facilitates chromatin remodeling subunit

protein-coding

Homo sapiens

基因描述

Type Description
Definition SPT16 homolog, facilitates chromatin remodeling subunit

研究结论

Date Results Publications
2021-04-17 13:15:00 Proteasomal Regulation of Mammalian SPT16 in Controlling Transcription. 33526453
2020-05-02 10:42:00 suggest a compelling mechanism for how FACT maintains chromatin integrity during polymerase passage, by facilitating removal of the H2A-H2B dimer, stabilizing intermediate subnucleosomal states and promoting nucleosome reassembly 31775157
2019-11-30 11:08:00 FACT subunit Spt16 controls UVSSA recruitment to lesion-stalled RNA Pol II and stimulates transcription-coupled nucleotide excision repair. 30715484
2019-09-21 12:30:00 Spt16 N-terminal domain is a histone H3-H4-specific binding domain with a distinct mechanism of interaction between histones and histone chaperones. 30528735
2019-03-16 11:12:00 We suggested that this constituted a new multiple congenital anomaly-intellectual disability syndrome due to defects in CHD8 and/or SUPT16H..The identification of multiple patients with the same genetic defect and characteristic clinical phenotype, confirms our suggestion that this is a syndromic disorder caused by haploinsufficiency or heterozygous loss of function of CHD8. 30670789

名称对应

Type IDs
Synonymous CDC68, FACTP140, SPT16, SPT16/CDC68
Gene
UniProtKB-ID: SP16H_HUMAN
UniprotKB: Q9Y5B9
UniParc: UPI0000035D5C
EMBL: BC064561, AF164924, BC073849, AF152961, BC014046, BC000565
Ensembl: ENSG00000092201
KO: hsa:11198
Nucleutide sequences
EMBL-CDS: AAF28231.1, AAH00565.1, AAD43978.1, AAH14046.1, AAH73849.1, AAH64561.1
Ensembl_TRS: ENST00000216297
Protein sequencees
Ensembl_PRO: ENSP00000216297
RefSeq: NP_009123.1, XP_011534683.1
Others
UniRef100: UniRef100_Q9Y5B9
UniRef90: UniRef90_Q9Y5B9
UniRef50: UniRef50_Q9Y5B9
UniGene: Hs.213724
CCDS: CCDS9569.1

全选

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