About   Help   FAQ
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
Export: Excel File
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory