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3199 HOXA2

3199

HOXA2

homeobox A2

protein-coding

Homo sapiens

基因描述

Type Description
Definition homeobox A2

研究结论

Date Results Publications
2021-03-20 13:26:00 lncRNA HOTAIRM1 promotes osteogenesis of hDFSCs by epigenetically regulating HOXA2 via DNMT1 in vitro. 32324272
2020-08-29 12:49:00 Identification of loss-of-function HOXA2 mutations in Chinese families with dominant bilateral microtia. 32649979
2020-01-18 12:04:00 our experiments support that PPP1CB and KPC2 together inhibit the activity of HOXA2 by activating its nuclear export, but favored HOXA2 de-ubiquitination and stabilization thereby establishing a store of HOXA2 in the cytoplasm. 31323436
2018-02-24 11:52:00 Performed mutational analysis of TCOF1, GSC, and HOXA2 to determine the mutational features of the 3 genes in Chinese patients with Treacher Collins syndrome. 27526242
2017-06-03 10:55:00 The role of HOXA2 gene in dominant isolated microtia and the dysmorphogenetic effect of this gene on ear development 27503514

名称对应

Type IDs
Synonymous HOX1K, MCOHI
Gene
UniProtKB-ID: HXA2_HUMAN
UniprotKB: O43364
UniParc: UPI0000049C49
EMBL: AC004079, BC136500, CH236948, BC130571, CH471073
Ensembl: ENSG00000105996
KO: hsa:3199
Nucleutide sequences
EMBL-CDS: AAI36501.1, EAL24227.1, EAW93864.1, AAI30572.1, AAS00375.1
Ensembl_TRS: ENST00000222718
Protein sequencees
Ensembl_PRO: ENSP00000222718
RefSeq: NP_006726.1
Others
UniRef100: UniRef100_O43364
UniRef90: UniRef90_O43364
UniRef50: UniRef50_P31245
UniGene: Hs.445239, Hs.592177
CCDS: CCDS5403.1

全选

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研究热度

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