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Symbol
Name
ID

Dcc
DCC netrin 1 receptor
MGI:94869

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 DCC
congenital mirror movement disorder

Mouse Phenotypes

nervous system phenotype

abnormal axon guidance

abnormal brain morphology

absent corpus callosum

absent hippocampal commissure

abnormal pyramidal decussation morphology

abnormal pontine nuclei morphology

abnormal optic nerve innervation

abnormal corticospinal tract morphology

ectopic neuron

abnormal optic nerve morphology

abnormal spinal cord dorsal column morphology

Availability

Mouse Genotype

Dcc^kanga/Dcc^kanga

Dcc^tm1.1Nki/Dcc^tm1.1Nki

Dcc^tm1Wbg/Dcc^tm1Wbg

*

Dcc^kanga/Dcc^tm1Wbg

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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