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Symbol
Name
ID

Fancd2
Fanconi anemia, complementation group D2
MGI:2448480

Phenotype annotations related to growth/size/body

!	Indicates phenotype varies with strain background.
	Darker colors indicate more annotations

Human Phenotypes	Umbilical hernia	Short stature	Small for gestational age	Weight loss	Growth delay	Intrauterine growth retardation
Disease(s) Associated with FANCD2	Umbilical hernia	Short stature	Small for gestational age	Weight loss	Growth delay	Intrauterine growth retardation
Fanconi anemia
Fanconi anemia complementation group D2

Mouse Phenotypes		decreased body weight	decreased body size	postnatal growth retardation	fetal growth retardation	enlarged spleen
Availability	Mouse Genotype	decreased body weight	decreased body size	postnatal growth retardation	fetal growth retardation	enlarged spleen
	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)
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