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Symbol
Name
ID

Setd1a
SET domain containing 1A
MGI:2446244

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Oligohydramnios
Disease(s) Associated with SETD1A	Oligohydramnios
neurodevelopmental disorder with speech impairment and dysmorphic facies

Mouse Phenotypes		failure to gastrulate	embryonic growth retardation
Availability	Mouse Genotype	failure to gastrulate	embryonic growth retardation
	Setd1a^tm1.2Afst/Setd1a^tm1.2Afst
	Setd1a^tm1Afst/Setd1a^tm1Afst
	Setd1a^tm1.1Afst/Setd1a^tm1.2Afst Tg(Gdf9-icre)5092Coo/0 (conditional)

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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