Cntn1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cntn1
contactin 1
MGI:105980

34 phenotypes from 3 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cntn1^m1J/Cntn1^m1J B6;C-Cntn1^m1J/GrsrJ	abnormal motor coordination/balance	J:178817
	ataxia	J:178817
	decreased body weight	J:178817
	lethality at weaning, complete penetrance	J:178817
	normal muscle phenotype	J:178817
	normal nervous system phenotype	J:178817
	preweaning lethality, incomplete penetrance	J:178817
	normal vision/eye phenotype	J:178817
Cntn1^tm1Brns/Cntn1^tm1Brns involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6	abnormal axon fasciculation	J:58556
	abnormal axon guidance	J:58556
	abnormal cerebellar Golgi cell morphology	J:58556
	abnormal cerebellar granule cell morphology	J:58556
	abnormal cerebellar granule layer morphology	J:58556
	abnormal cerebellar molecular layer	J:58556
	abnormal cerebellum morphology	J:58556
	abnormal dendrite morphology	J:58556
	abnormal gait	J:58556
	abnormal motor capabilities/coordination/movement	J:58556
	abnormal motor coordination/balance	J:58556
	abnormal posture	J:58556
	abnormal Purkinje cell axon morphology	J:58556
	ataxia	J:58556
	normal behavior/neurological phenotype	J:58556
	cachexia	J:58556
	decreased body size	J:58556
	impaired limb coordination	J:58556
	postnatal lethality, complete penetrance	J:58556
	small cerebellum	J:58556
	weakness	J:58556
	weight loss	J:58556
Cntn1^usl/Cntn1^usl B6.MRL-Cntn1^usl/GrsrJ	abnormal limb posture	J:203032
	abnormal motor coordination/balance	J:203032
	ataxia	J:203032
	decreased body size	J:203032
	prenatal lethality, incomplete penetrance	J:203032
	preweaning lethality, complete penetrance	J:203032
Cntn1^usl/Cntn1^usl MRL/MpJ-Fas^lpr Cntn1^usl/GrsrJ	abnormal cerebellar granule cell morphology	J:203032
	abnormal limb posture	J:203032
	abnormal motor coordination/balance	J:203032
	ataxia	J:203032
	circling	J:203032
	decreased body size	J:203032
	gliosis	J:203032
	prenatal lethality, incomplete penetrance	J:203032
	preweaning lethality, complete penetrance	J:203032
	stomach non-glandular epithelium hyperkeratosis	J:203032
	normal vision/eye phenotype	J:203032

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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