|
Symbol Name ID |
Cntn1
contactin 1 MGI:105980 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Areflexia |
Akinesia |
Global developmental delay |
| Disease(s) Associated with CNTN1 | |||
| Compton-North congenital myopathy |
| Mouse Phenotypes | nervous system phenotype |
abnormal axon fasciculation |
abnormal axon guidance |
abnormal cerebellum morphology |
abnormal Purkinje cell axon morphology |
abnormal cerebellar granule layer morphology |
abnormal cerebellar Golgi cell morphology |
abnormal cerebellar granule cell morphology |
abnormal cerebellar molecular layer |
small cerebellum |
gliosis |
abnormal dendrite morphology |
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| Availability | Mouse Genotype | ||||||||||||
| Cntn1m1J/Cntn1m1J | * | ||||||||||||
| Cntn1tm1Brns/Cntn1tm1Brns | |||||||||||||
| Cntn1usl/Cntn1usl | |||||||||||||
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 04/23/2024 MGI 6.23 |
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