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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

Abnormality of the eye

Astigmatism

Cataract

Aplasia/Hypoplasia of the iris

Hypertelorism

Hypotelorism

Proptosis

Microphthalmia

Strabismus

Nystagmus

Abnormality of vision

Visual impairment

Ptosis

Disease(s) Associated with FANCD2

Fanconi anemia

Fanconi anemia complementation group D2

Mouse Phenotypes		abnormal retina blood vessel morphology	abnormal lens development	aphakia	abnormal retina development	persistence of hyaloid vascular system	microphthalmia
Availability	Mouse Genotype	abnormal retina blood vessel morphology	abnormal lens development	aphakia	abnormal retina development	persistence of hyaloid vascular system	microphthalmia
	Fancd2^em1Tzh/Fancd2^em1Tzh
	Fancd2^{Gt(OST57859)Lex}/Fancd2^{Gt(OST57859)Lex}
	Fancd2^tm1Hou/Fancd2^tm1Hou
	Fancd2^{em1(IMPC)Hmgu}/Fancd2⁺

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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