Symbol
Name
ID

Kptn
kaptin
MGI:1890380

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes

Ventriculomegaly

Delayed speech and language development

Anxiety

Autistic behavior

Motor stereotypy

Self-injurious behavior

Intellectual disability

Global developmental delay

Motor delay

Bilateral tonic-clonic seizure

Generalized non-motor (absence) seizure

Generalized-onset seizure

Disease(s) Associated with KPTN

autosomal recessive intellectual developmental disorder 41

Mouse Phenotypes		increased brain size	small lateral ventricles	increased corpus callosum size	increased brain internal capsule size	small hippocampus	increased cerebral cortex cell number	increased cerebral cortex total cell area	increased primary motor cortex size	thickened cerebral cortex	abnormal brain physiology
Availability	Mouse Genotype
	Kptn^{tm1a(EUCOMM)Wtsi}/Kptn^{tm1a(EUCOMM)Wtsi}

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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