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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Cntnap1
contactin associated protein-like 1
MGI:1858201
40 phenotypes from 11 alleles in 9 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Ccr10/Cntnap1tm1Bhat/Ccr10/Cntnap1tm1Bhat
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, 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
Cntnap1em1Bhat/Ccr10/Cntnap1tm1Bhat
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 coordination J:342323
muscle weakness J:342323
paresis J:342323
tremors J:342323
Cntnap1em2Bhat/Ccr10/Cntnap1tm1Bhat
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 coordination J:342323
muscle weakness J:342323
paresis J:342323
tremors J:342323
Cntnap1M1Btlr/Cntnap1+
C57BL/6J-Cntnap1M1Btlr 		decreased body weight J:255017
Cntnap1M1Btlr/Cntnap1M1Btlr
C57BL/6J-Cntnap1M1Btlr 		decreased body weight J:255017
Cntnap1shm-3J/Cntnap1shm-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
Cntnap1shm-4J/Cntnap1shm-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
Cntnap1shm-5J/Cntnap1shm-5J
B6.Cg-Cntnap1shm-5J/GrsrJ 		abnormal gait J:181679
abnormal limb posture J:181679
decreased body size J:181679
reduced male fertility J:181679
tremors J:181679
Cntnap1shm/Cntnap1shm-2J
Not Specified 		abnormal gait J:84767
abnormal motor coordination/balance J:84767
ataxia J:84767
tremors J:84767
Cntnap1shm/Cntnap1shm
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
Cntnap1shm/Cntnap1shm
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
Cntnap1tm1Bhat/Cntnap1tm1Bhat
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
Cntnap1tm1Pele/Cntnap1tm1Pele
involves: ICR 		ataxia J:166099
decreased nerve conduction velocity J:166099
tremors J:166099
Cntnap1tm1Pele/Cntnap1tm1Pele
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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11/12/2024
MGI 6.24 		The Jackson Laboratory