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Symbol
Name
ID

Phox2b
paired-like homeobox 2b
MGI:1100882

Phenotype annotations related to respiratory system

Darker colors indicate more annotations

Human Phenotypes	Hypercapnia	Hypoxemia	Apnea	Respiratory distress	Hypoventilation	Central hypoventilation	Nocturnal hypoventilation	Respiratory insufficiency
Disease(s) Associated with PHOX2B	Hypercapnia	Hypoxemia	Apnea	Respiratory distress	Hypoventilation	Central hypoventilation	Nocturnal hypoventilation	Respiratory insufficiency
congenital central hypoventilation syndrome
neuroblastoma

Mouse Phenotypes		abnormal respiration	abnormal lung volume	abnormal respiratory function	abnormal breathing pattern	decreased pulmonary respiratory rate	apnea	abnormal pulmonary ventilation	decreased pulmonary ventilation	hypoventilation	respiratory failure
Availability	Mouse Genotype	abnormal respiration	abnormal lung volume	abnormal respiratory function	abnormal breathing pattern	decreased pulmonary respiratory rate	apnea	abnormal pulmonary ventilation	decreased pulmonary ventilation	hypoventilation	respiratory failure
	Phox2b^tm1.1Heno/Phox2b⁺
	Phox2b^tm1Jbr/Phox2b⁺
	Phox2b^tm2.1Heno/Phox2b⁺
	Phox2b^tm2Jbr/Phox2b⁺
	Egr2^tm2(cre)Pch/Egr2⁺ Phox2b^tm4Jbr/Phox2b⁺ (conditional)
	Phox2b^tm1Rth/Phox2b⁺ Hprt1^{tm1(CAG-cre)Mnn}/? (conditional)
	Phox2b^tm1Rth/Phox2b⁺ Tg(Fabp7-cre,-lacZ)3Gtm/0 (conditional)
	Phox2b^tm4Jbr/Phox2b⁺ Tg(Pgk1-cre)1Lni/0 (conditional)

Contributing Projects: 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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