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Symbol
Name
ID

Smn1
survival motor neuron 1
MGI:109257

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement
Disease(s) Associated with SMN1	Decreased fetal movement
Werdnig-Hoffmann disease

Mouse Phenotypes		embryonic growth arrest	embryonic growth retardation	abnormal embryonic tissue morphology	absent blastocoele
Availability	Mouse Genotype	embryonic growth arrest	embryonic growth retardation	abnormal embryonic tissue morphology	absent blastocoele
	Smn1^tm1Cdid/Smn1^tm1Cdid
	Smn1^tm1Msd/Smn1^tm1Msd
	Smn1^tm2Cdid/Smn1^tm2Cdid

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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