Symbol
Name
ID

Slitrk2
SLIT and NTRK-like family, member 2
MGI:2679449

Phenotype annotations related to nervous system

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

Human Phenotypes

Spasticity

Ventriculomegaly

Hippocampal atrophy

Thin corpus callosum

Corpus callosum atrophy

Reduced cerebral white matter volume

Cerebral palsy

Phonic tics

Absent speech

Delayed speech and language development

Anxiety

Autistic behavior

Aggressive behavior

Compulsive behaviors

Hyperactivity

Intellectual disability

Dystonia

Unsteady gait

Global developmental delay

Seizure

Disease(s) Associated with SLITRK2

non-syndromic X-linked intellectual developmental disorder 111

Mouse Phenotypes		nervous system phenotype	abnormal serotonergic neuron morphology	abnormal synapse morphology	abnormal postsynaptic density morphology	abnormal excitatory synapse morphology	abnormal excitatory postsynaptic potential	abnormal miniature excitatory postsynaptic currents
Availability	Mouse Genotype	nervous system phenotype	abnormal serotonergic neuron morphology	abnormal synapse morphology	abnormal postsynaptic density morphology	abnormal excitatory synapse morphology	abnormal excitatory postsynaptic potential	abnormal miniature excitatory postsynaptic currents
	Slitrk2^tm1.1Jaru/Slitrk2^tm1.1Jaru	*
	Slitrk2^tm1.1Jwum/Y Tg(Nes-cre)1Atp/0 (conditional)
	Slitrk2^tm1.1Jwum/Y (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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