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Symbol
Name
ID

Neurod2
neurogenic differentiation 2
MGI:107755

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Dysphagia

Delayed CNS myelination

Hypoplasia of the corpus callosum

Periventricular white matter hyperintensities

Cerebral atrophy

Hypsarrhythmia

Reduced eye contact

Inability to walk

Hyperkinetic movements

Epileptic encephalopathy

Global developmental delay

Delayed ability to sit

Delayed ability to walk

Infantile spasms

Disease(s) Associated with NEUROD2

developmental and epileptic encephalopathy 72

Mouse Phenotypes		increased susceptibility to pharmacologically induced seizures	tonic-clonic seizures	sporadic seizures	small cerebellum	decreased prepulse inhibition
Availability	Mouse Genotype		tonic-clonic seizures	sporadic seizures	small cerebellum	decreased prepulse inhibition
	Neurod2^{em1(IMPC)Hmgu}/Neurod2^{em1(IMPC)Hmgu}
	Neurod2^tm1Tap/Neurod2^tm1Tap
	Neurod2^tm1Tap/Neurod2⁺

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 04/23/2024 MGI 6.23