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Symbol
Name
ID

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

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Polyhydramnios
Disease(s) Associated with ESCO2	Polyhydramnios
Roberts syndrome

Mouse Phenotypes		abnormal preimplantation embryo development	abnormal embryonic neuroepithelium morphology
Availability	Mouse Genotype	abnormal preimplantation embryo development	abnormal embryonic neuroepithelium morphology
	Esco2^tm1.2Ge/Esco2^tm1.2Ge
	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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