Symbol
Name
ID

Pcdh19
protocadherin 19
MGI:2685563

Phenotype annotations related to nervous system

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes

Ventriculomegaly

Delayed speech and language development

Anxiety

Psychosis

Atypical behavior

Abnormal social behavior

Autistic behavior

Abnormal eating behavior

Aggressive behavior

Compulsive behaviors

Hyperactivity

Attention deficit hyperactivity disorder

Impulsivity

Intellectual disability

Intellectual disability, mild

Intellectual disability, moderate

Intellectual disability, profound

Intellectual disability, severe

Developmental regression

Global developmental delay

Motor delay

Bilateral tonic-clonic seizure

Bilateral tonic-clonic seizure with generalized onset

Convulsive status epilepticus

Generalized non-motor (absence) seizure

Atypical absence seizure

Focal-onset seizure

Focal hemiclonic seizure

Focal sensory seizure with cephalic sensation

Generalized clonic seizure

Generalized myoclonic seizure

Generalized tonic seizure

Febrile seizure (within the age range of 3 months to 6 years)

Complex febrile seizure

Atonic seizure

Status epilepticus

Disease(s) Associated with PCDH19

developmental and epileptic encephalopathy 9

Mouse Phenotypes		nervous system phenotype	abnormal neuronal migration	abnormal forebrain development	abnormal brain wave pattern
Availability	Mouse Genotype	nervous system phenotype	abnormal neuronal migration	abnormal forebrain development	abnormal brain wave pattern
	Pcdh19^tm1Tac/Pcdh19^tm1Tac	*
	Pcdh19^tm1Tac/Pcdh19⁺	*
	Pcdh19^tm1Tac/Pcdh19^em1Pqt
	Pcdh19^tm1Tac/Y	*

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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