Symbol Name ID |
Phox2b
paired-like homeobox 2b MGI:1100882 |
Darker colors indicate more annotations |
Human Phenotypes | Increased circulating ferritin concentration |
Increased circulating lactate dehydrogenase concentration |
Abnormality of temperature regulation |
Fever |
Elevated urinary homovanillic acid |
Elevated urinary vanillylmandelic acid |
Elevated urinary catecholamine level |
Elevated circulating catecholamine level |
Disease(s) Associated with PHOX2B | ||||||||
congenital central hypoventilation syndrome | ||||||||
neuroblastoma |
Mouse Phenotypes | alkalemia |
cyanosis |
abnormal noradrenaline level |
|
Availability | Mouse Genotype | |||
Phox2btm1(Phox2a)Mist/Phox2btm1(Phox2a)Mist | ||||
Phox2btm1Jbr/Phox2btm1Jbr | ||||
Phox2btm1.1Heno/Phox2b+ | ||||
Phox2btm2.1Heno/Phox2b+ | ||||
Phox2btm2Jbr/Phox2b+ | ||||
Egr2tm2(cre)Pch/Egr2+ Phox2btm4Jbr/Phox2b+ (conditional) |
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Phox2btm1Rth/Phox2b+ Hprt1tm1(CAG-cre)Mnn/? (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 08/02/2024 MGI 6.24 |
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