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Symbol
Name
ID

Esco2
establishment of sister chromatid cohesion N-acetyltransferase 2
MGI:1919238

Phenotype annotations related to growth/size/body

Darker colors indicate more annotations

Human Phenotypes	Cystic hygroma	Short neck	Severe intrauterine growth retardation	Postnatal growth retardation
Disease(s) Associated with ESCO2
Roberts syndrome

Mouse Phenotypes		microcephaly
Availability	Mouse Genotype	microcephaly
	Emx1^tm1(cre)Krj/Emx1⁺ Esco2^tm1.1Ge/Esco2^tm1.1Ge (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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