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Symbol
Name
ID

Fancd2
Fanconi anemia, complementation group D2
MGI:2448480

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Hypertelorism	Hypotelorism	Microphthalmia	Strabismus
Disease(s) Associated with FANCD2
Fanconi anemia complementation group D2

Mouse Phenotypes		abnormal lens development	aphakia	abnormal retinal development	microphthalmia
Availability	Mouse Genotype	abnormal lens development	aphakia	abnormal retinal development	microphthalmia
	Fancd2^em1Tzh/Fancd2^em1Tzh
	Fancd2^{Gt(OST57859)Lex}/Fancd2^{Gt(OST57859)Lex}
	Fancd2^tm1Hou/Fancd2^tm1Hou

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)
Citing These Resources Funding Information Warranty Disclaimer & Copyright Notice Send questions and comments to User Support.	last database update 02/16/2021 MGI 6.16