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Phenotypes Associated with This Genotype
Genotype
MGI:5523900
Allelic
Composition
Cntn1usl/Cntn1usl
Genetic
Background
B6.MRL-Cntn1usl/GrsrJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cntn1usl mutation (1 available); any Cntn1 mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• homozygotes splay their hind legs, stagger from side-to-side, and a few may lean their head to the side or circle slowly
• hind limbs can be splayed

mortality/aging
• lower than expected Mendelian ratio of homozygotes from heterozgyous intercross indicates embryonic or perinatal lethality
• all homozygotes die by 3 weeks of age

growth/size/body
• runted body size and lack of vitality

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Compton-North congenital myopathy DOID:0080101 OMIM:612540
J:222308


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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last database update
02/23/2021
MGI 6.16
The Jackson Laboratory