Cntnap1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cntnap1
contactin associated protein-like 1
MGI:1858201

41 phenotypes from 11 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Ccr10/Cntnap1^tm1Bhat/Ccr10/Cntnap1^tm1Bhat involves: 129S7/SvEvBrd	abnormal action potential	J:69621
	abnormal axon morphology	J:69621
	abnormal cerebellar molecular layer	J:162215
	abnormal gait	J:69621, J:107653
	abnormal myelin sheath morphology	J:69621, J:162215
	abnormal nerve conduction	J:342323
	abnormal Purkinje cell axon morphology	J:107653, J:162215
	abnormal Purkinje cell morphology	J:107653, J:162215
	ataxia	J:69621, J:107653
	cerebellum atrophy	J:162215
	decreased body size	J:69621
	decreased body weight	J:69621
	decreased locomotor activity	J:69621
	decreased nerve conduction velocity	J:69621, J:342323
	dysmyelination	J:342323
	hypermyelination	J:69621
	impaired balance	J:69621
	impaired coordination	J:107653
	impaired fine motor coordination	J:342323
	kyphosis	J:69621
	lethality at weaning, incomplete penetrance	J:69621
	muscle spasm	J:69621
	paresis	J:69621
	premature death	J:69621
	tremors	J:69621
	weakness	J:69621
Cntnap1^em1Bhat/Ccr10/Cntnap1^tm1Bhat involves: 129S7/SvEvBrd	abnormal nerve conduction	J:342323
	abnormal paranodal axoglial junction morphology	J:342323
	abnormal paranode morphology	J:342323
	decreased body weight	J:342323
	decreased locomotor activity	J:342323
	decreased nerve conduction velocity	J:342323
	dysmyelination	J:342323
	impaired fine motor coordination	J:342323
	muscle weakness	J:342323
	paresis	J:342323
	tremors	J:342323
Cntnap1^em2Bhat/Ccr10/Cntnap1^tm1Bhat involves: 129S7/SvEvBrd	abnormal nerve conduction	J:342323
	abnormal paranodal axoglial junction morphology	J:342323
	abnormal paranode morphology	J:342323
	decreased body weight	J:342323
	decreased locomotor activity	J:342323
	decreased nerve conduction velocity	J:342323
	dysmyelination	J:342323
	impaired fine motor coordination	J:342323
	muscle weakness	J:342323
	paresis	J:342323
	tremors	J:342323
Cntnap1^M1Btlr/Cntnap1⁺ C57BL/6J-Cntnap1^M1Btlr	decreased body weight	J:255017
Cntnap1^M1Btlr/Cntnap1^M1Btlr C57BL/6J-Cntnap1^M1Btlr	decreased body weight	J:255017
Cntnap1^shm-3J/Cntnap1^shm-3J involves: C3H/HeJ	abnormal gait	J:16313
	abnormal motor coordination/balance	J:16313
	abnormal resting posture	J:16313
	ataxia	J:16313
	tremors	J:16313
Cntnap1^shm-4J/Cntnap1^shm-4J involves: C3H/HeDiSn * Swiss stock	abnormal gait	J:16313
	abnormal motor coordination/balance	J:16313
	abnormal resting posture	J:16313
	ataxia	J:16313
	tremors	J:16313
Cntnap1^shm-5J/Cntnap1^shm-5J B6.Cg-Cntnap1^shm-5J/GrsrJ	abnormal gait	J:181679
	abnormal limb posture	J:181679
	decreased body size	J:181679
	reduced male fertility	J:181679
	tremors	J:181679
Cntnap1^shm/Cntnap1^shm-2J Not Specified	abnormal gait	J:84767
	abnormal motor coordination/balance	J:84767
	ataxia	J:84767
	tremors	J:84767
Cntnap1^shm/Cntnap1^shm involves: BALB/cJ * C3HeB/FeJ * C57BL/6J * DBA/2J	abnormal gait	J:5040
	abnormal motor coordination/balance	J:5040
	abnormal resting posture	J:5040
	ataxia	J:5040
	decreased body size	J:5040
	decreased locomotor activity	J:5040
	decreased survivor rate	J:5217
	impaired coordination	J:5040
	impaired swimming	J:5040
	reduced fertility	J:5040
	tremors	J:5040
Cntnap1^shm/Cntnap1^shm SHM/Nem	abnormal axon morphology	J:165697
	abnormal gait	J:165697
	abnormal limb posture	J:165697
	abnormal nerve conduction	J:165697
	abnormal node of Ranvier morphology	J:165697
	abnormal paranodal axoglial junction morphology	J:165697
	abnormal paranode morphology	J:165697
	abnormal visual evoked potential	J:165697
	ataxia	J:165697
	decreased body size	J:165697
	decreased locomotor activity	J:165697
	decreased nerve conduction velocity	J:165697
	impaired limb coordination	J:165697
	lethality at weaning, complete penetrance	J:165697
	tremors	J:165697
Cntnap1^tm1Bhat/Cntnap1^tm1Bhat involves: 129S7/SvEvBrd	abnormal action potential	J:107653
	abnormal axon morphology	J:107653
	abnormal gait	J:107653
	abnormal myelin sheath morphology	J:107653
	ataxia	J:107653
	decreased body size	J:107653
	decreased body weight	J:107653
	decreased locomotor activity	J:107653
	decreased nerve conduction velocity	J:107653
	hypermyelination	J:107653
	kyphosis	J:107653
	lethality at weaning, incomplete penetrance	J:107653
	muscle spasm	J:107653
	normal nervous system phenotype	J:107653
	paresis	J:107653
	premature death	J:107653
	tremors	J:107653
	weakness	J:107653
Cntnap1^tm1Pele/Cntnap1^tm1Pele involves: ICR	ataxia	J:166099
	decreased nerve conduction velocity	J:166099
	tremors	J:166099
Cntnap1^tm1Pele/Cntnap1^tm1Pele Not Specified	abnormal axon morphology	J:87070

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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