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Symbol
Name
ID

Ift122
intraflagellar transport 122
MGI:1932386

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Retinal dystrophy	Hypotelorism	Nystagmus	Myopia
Disease(s) Associated with IFT122
cranioectodermal dysplasia 1

Mouse Phenotypes		abnormal eye morphology	abnormal eye development
Availability	Mouse Genotype	abnormal eye morphology	abnormal eye development
	Ift122^sopb/Ift122^sopb
	Mbd4/Ift122^tm1Abc/Mbd4/Ift122^tm1Abc

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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