Symbol Name ID |
Dcc
DCC netrin 1 receptor MGI:94869 |
* | 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 |
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Availability | Mouse Genotype | ||||||||||||
Dcckanga/Dcckanga | |||||||||||||
Dcctm1.1Nki/Dcctm1.1Nki | |||||||||||||
Dcctm1Wbg/Dcctm1Wbg | * | ||||||||||||
Dcckanga/Dcctm1Wbg |
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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last database update 07/05/2024 MGI 6.24 |
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