Symbol
Name
ID

Ntn1
netrin 1
MGI:105088

Phenotype annotations related to nervous system

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

Human Phenotypes	Easy fatigability	Agenesis of corpus callosum	Dysgenesis of the hippocampus	Abnormal corticospinal tract morphology	Clumsiness	Poor fine motor coordination	Cerebral palsy	Intellectual disability, mild	Abnormality of movement	Bimanual synkinesia	Specific learning disability
Disease(s) Associated with NTN1
congenital mirror movement disorder

Mouse Phenotypes

nervous system phenotype

abnormal axon guidance

abnormal brain commissure morphology

absent corpus callosum

absent hippocampal commissure

abnormal anterior commissure morphology

abnormal pyramidal decussation morphology

abnormal pontine nuclei morphology

abnormal spinal cord ependymal layer morphology

abnormal corticospinal tract morphology

abnormal spinal cord ventral commissure morphology

abnormal dorsal spinal root morphology

abnormal spinal cord central canal morphology

abnormal spinal cord dorsal column morphology

Availability

Mouse Genotype

Ntn1^{Gt(IRESBetageo)1Pgr}/Ntn1^{Gt(IRESBetageo)1Pgr}

Ntn1^Gt(ST629)Byg/Ntn1^Gt(ST629)Byg

Ntn1^tm1.2Tek/Ntn1^tm1.2Tek

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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