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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mycbp2m7Bei
mutation 7 David R Beier
MGI:5505462
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Mycbp2m7Bei/Mycbp2m7Bei
Cntn2tm1Furl/Cntn2+
involves: 129S1/Sv * A/J * C57BL/6 MGI:5505464


Genotype
MGI:5505464
cx1
Allelic
Composition
Mycbp2m7Bei/Mycbp2m7Bei
Cntn2tm1Furl/Cntn2+
Genetic
Background
involves: 129S1/Sv * A/J * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cntn2tm1Furl mutation (1 available); any Cntn2 mutation (53 available)
Mycbp2m7Bei mutation (1 available); any Mycbp2 mutation (223 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• midline crossing defect occasionally
• aberrant patterning in the striatum
• corticofugal axon tracts in the ventral striatum

limbs/digits/tail





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
05/07/2024
MGI 6.23
The Jackson Laboratory