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Symbol
Name
ID

Phox2b
paired-like homeobox 2b
MGI:1100882

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Proptosis	Horner syndrome	Opsoclonus
Disease(s) Associated with PHOX2B
neuroblastoma

Mouse Phenotypes		impaired pupillary reflex	abnormal eye morphology	mydriasis
Availability	Mouse Genotype	impaired pupillary reflex	abnormal eye morphology	mydriasis
	Phox2b^Dilp1/Phox2b⁺
	Phox2b^tm1Jbr/Phox2b⁺

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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