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Symbol
Name
ID

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

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Microcephaly	Frontal encephalocele	Hydrocephalus	Cranial nerve paralysis	Intellectual disability	Global developmental delay
Disease(s) Associated with ESCO2
Roberts syndrome

Mouse Phenotypes		increased neuron apoptosis	abnormal neuronal precursor proliferation	abnormal embryonic neuroepithelium morphology	abnormal hippocampus development	absent hippocampus	abnormal neocortex morphology
Availability	Mouse Genotype
	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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/16/2024 MGI 6.23