Type | Description |
---|---|
Definition | paired-like homeobox 2b |
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 |
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
|
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Refseq |
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