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18935 Phox2b

18935

Phox2b

paired-like homeobox 2b

protein-coding

Mus musculus

基因描述

Type Description
Definition paired-like homeobox 2b

研究结论

Date Results Publications
2020-10-31 13:16:00 Rnf220/Zc4h2-mediated monoubiquitylation of Phox2 is required for noradrenergic neuron development. 32094113
2020-06-20 11:45:00 The paired-like homeobox 2b gene (Phox2b) is the disease-defining gene for congenital central hypoventilation syndrome and is restrictively present in brainstem nucleus 30626698
2018-06-09 12:11:00 This study demonstrated that the Phox2b distinguishes between oral and non-oral sensory neurons in the geniculate ganglion in mice. 28856690
2017-09-09 14:07:00 Murine models of congenital central hypoventilation syndrome designed with PHOX2B mutations have suggested RTN neuron agenesis. 27226447
2016-01-16 11:39:00 The retrotrapezoid nucleus neurons expressing Atoh1 and Phox2b are essential for the respiratory response to CO2. 25866925

名称对应

Type IDs
Synonymous Dilp1, NBPhox, Pmx2b, Px2b
Gene
UniProtKB-ID: PHX2B_MOUSE
UniprotKB: O35690
UniParc: UPI000000D936
EMBL: Y14493, BC079610, AB015672
Ensembl: ENSMUSG00000012520
KO: mmu:18935
Nucleutide sequences
EMBL-CDS: CAA74833.1, AAH79610.1, BAA82671.1
Ensembl_TRS: ENSMUST00000012664
Protein sequencees
Ensembl_PRO: ENSMUSP00000012664
RefSeq: NP_032914.1
Others
UniRef100: UniRef100_Q99453
UniRef90: UniRef90_Q99453
UniRef50: UniRef50_Q99453
UniGene: Mm.62505
CCDS: CCDS19316.1

全选

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研究热度

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