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Symbol
Name
ID

Cntn1
contactin 1
MGI:105980

Phenotype annotations related to behavior/neurological

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

Human Phenotypes	Decreased fetal movement	Fetal akinesia sequence	Feeding difficulties	Poor suck
Disease(s) Associated with CNTN1
Compton-North congenital myopathy

Mouse Phenotypes		behavior/neurological phenotype	abnormal motor capabilities/coordination/movement	abnormal motor coordination/balance	ataxia	impaired limb coordination	weakness	abnormal posture	abnormal limb posture	abnormal gait	circling
Availability	Mouse Genotype	behavior/neurological phenotype	abnormal motor capabilities/coordination/movement	abnormal motor coordination/balance	ataxia	impaired limb coordination	weakness	abnormal posture	abnormal limb posture	abnormal gait	circling
	Cntn1^m1J/Cntn1^m1J
	Cntn1^tm1Brns/Cntn1^tm1Brns	*
	Cntn1^usl/Cntn1^usl

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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