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84627 ZNF469

84627

ZNF469

zinc finger protein 469

protein-coding

Homo sapiens

基因描述

Type Description
Definition zinc finger protein 469

研究结论

Date Results Publications
2019-08-24 12:36:00 CXL may be associated with the development of corneal perforation in particular at-risk individuals with keratoconus. Identifying clinical and genetic risk factors, including screening of ZNF469 and PRDM5, may be useful in the prevention of significant complications after CXL. 31107761
2019-06-22 10:10:00 This is the first report of a ZNF469 homozygous mutation causing a Brittle cornea syndrome phenotype in a consanguineous Pakistani family. 30865045
2019-03-02 10:34:00 Linc-ZNF469-3 promotes lung metastasis of TNBC through miR-574-5p-ZEB1 signaling axis. 29755127
2018-07-21 10:29:00 genotype frequencies did not differ between the sporadic or familial keratoconus cases 29187250
2018-04-14 10:25:00 ZNF469 has a pathogenic role in Chinese patients with keratoconus. 28484309

名称对应

Type IDs
Synonymous BCS, BCS1
Gene
UniProtKB-ID: H3BS19_HUMAN
UniprotKB: H3BS19
UniParc: UPI0004620D6A
EMBL: KF456226, AC135049, AC132804
Ensembl: ENSG00000225614
Nucleutide sequences
Ensembl_TRS: ENST00000565624
Protein sequencees
Ensembl_PRO: ENSP00000456500
RefSeq: XP_016879273.1, NP_001354553.1
Others
UniRef100: UniRef100_H3BS19
UniRef90: UniRef90_Q96JG9
UniRef50: UniRef50_Q96JG9
UniGene: Hs.54925

全选

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研究热度

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