- kyphosis / MGI
- muscle spasm / MGI
- tremors / MGI
- weakness / MGI
- paresis / MGI
- abnormal Purkinje cell morphology / MGI
- abnormal cerebellar molecular layer / MGI
- decreased body weight / MGI
- decreased body size / MGI
- ataxia / MGI
- hypoactivity / MGI
- impaired coordination / MGI
- abnormal gait / MGI
- abnormal motor coordination/balance / MGI
- impaired swimming / MGI
- impaired limb coordination / MGI
- impaired balance / MGI
- reduced fertility / MGI
- reduced male fertility / MGI
- premature death / MGI
- nervous system phenotype / MGI
- abnormal myelin sheath morphology / MGI
- abnormal limb posture / MGI
- abnormal action potential / MGI
- abnormal nerve conduction / MGI
- abnormal axon morphology / MGI
- decreased survivor rate / MGI
- decreased nerve conduction velocity / MGI
- abnormal resting posture / MGI
- hypermyelination / MGI
- abnormal node of Ranvier morphology / MGI
- abnormal paranode morphology / MGI
- abnormal paranodal axoglial junction morphology / MGI
- abnormal visual evoked potential / MGI
- lethality at weaning, complete penetrance / MGI
- lethality at weaning, incomplete penetrance / MGI
- cerebellum atrophy / MGI
C57BL/6NTac-Cntnap1tm1a(EUCOMM)Wtsi/IcsOrl
Status | Available to order |
EMMA ID | EM:09950 |
International strain name | C57BL/6NTac-Cntnap1tm1a(EUCOMM)Wtsi/IcsOrl |
Alternative name | EPD0198_2_B10 |
Strain type | Targeted Mutant Strains |
Allele/Transgene symbol | Cntnap1tm1a(EUCOMM)Wtsi |
Gene/Transgene symbol | Cntnap1 |
Disclaimer | Please note that for EUCOMM and KOMP-CSD mice supplied to the scientific community by INFRAFRONTIER/EMMA:
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Information from provider
Provider | ICS, Institut Clinique de la Souris |
Provider affiliation | ICS, Institut Clinique de la Souris |
Genetic information | This mouse line originates from EUCOMM ES clone EPD0198_2_B10. For further details on the construction of this clone see the page at the IKMC portal. |
Phenotypic information | Potential phenotyping data in the IMPC portal |
References | None available |
Information from EMMA
Archiving centre | Institut de Transgenose, INTRAGENE, Orléans, France |
Animals used for archiving | heterozygous C57BL/6NTac |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Hypomyelination neuropathy-arthrogryposis syndrome / Orphanet_2680
MGI phenotypes (gene matching)
Information on how we integrate external resources can be found here
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