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Symbol
Name
ID

Phox2b
paired-like homeobox 2b
MGI:1100882

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties	Bone pain	Fatigue
Disease(s) Associated with PHOX2B	Feeding difficulties	Bone pain	Fatigue
congenital central hypoventilation syndrome
neuroblastoma

Mouse Phenotypes		abnormal suckling behavior	impaired pupillary reflex
Availability	Mouse Genotype	abnormal suckling behavior	impaired pupillary reflex
	Phox2b^Dilp1/Phox2b⁺
	Phox2b^tm1Jbr/Phox2b⁺
	Phox2b^tm1Rth/Phox2b⁺ Tg(Fabp7-cre,-lacZ)3Gtm/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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