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Symbol
Name
ID

Copb2
COPI coat complex subunit beta 2
MGI:1354962

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Cerebral visual impairment
Disease(s) Associated with COPB2	Cerebral visual impairment
primary autosomal recessive microcephaly 19

Mouse Phenotypes		abnormal retina vasculature morphology
Availability	Mouse Genotype	abnormal retina vasculature morphology
	Copb2^em1(IMPC)Bay/Copb2⁺

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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