About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dab1tm2Cpr
targeted mutation 2, Jonathan A Cooper
MGI:2388292
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dab1tm2Cpr/Dab1tm2Cpr either: (involves: 129S4/SvJaeSor * BALB/c) or (involves: 129S4/SvJaeSor * C57BL/6) MGI:3722250
hm2
Dab1tm2Cpr/Dab1tm2Cpr involves: 129S4/SvJaeSor MGI:3810295
hm3
Dab1tm2Cpr/Dab1tm2Cpr involves: 129S4/SvJaeSor * C57BL/6 MGI:3722179
ht4
Dab1tm1Cpr/Dab1tm2Cpr involves: 129S4/SvJaeSor * C57BL/6 MGI:3722181


Genotype
MGI:3722250
hm1
Allelic
Composition
Dab1tm2Cpr/Dab1tm2Cpr
Genetic
Background
either: (involves: 129S4/SvJaeSor * BALB/c) or (involves: 129S4/SvJaeSor * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dab1tm2Cpr mutation (0 available); any Dab1 mutation (77 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• at P17 and P61, rostral migratory streams of (RMS) neuroblasts are severely disrupted and neuroblasts accumulate in the subventricular zone
• neuroblasts accumulate in the subventricular zone
• a 15-fold increase in apoptosis in the subventricular zone is observed




Genotype
MGI:3810295
hm2
Allelic
Composition
Dab1tm2Cpr/Dab1tm2Cpr
Genetic
Background
involves: 129S4/SvJaeSor
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dab1tm2Cpr mutation (0 available); any Dab1 mutation (77 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• the neocortical marginal zone is crowded with polymorphic cells unlike in wild-type mice
• the dentate gyrus is disrupted
• the pyramidal cells are scattered over a broad region unlike in wild-type mice




Genotype
MGI:3722179
hm3
Allelic
Composition
Dab1tm2Cpr/Dab1tm2Cpr
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dab1tm2Cpr mutation (0 available); any Dab1 mutation (77 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die at day 20 to 30 of unidentified causes

nervous system
• the cerebral cortex, hippocampus and cerebellum exhibit defects
• the cortical marginal zone is occupied with many cells unlike in wild-type mice
• the intermediate plexiform zone proximal to the pial surface contains ectopic nerve tracts
• only two or three wavy lamina form
• the granule cells in the dentate gyrus are disorganized
• the six layers of the cerebral cortex are disorganized
• the Purkinje cell layers are organized into internal clusters
• the cerebellar granule cells are found in a less organized layer than in wild-type mice and are excluded from the external limits of the cerebellum by a thin molecular layer
• the cerebellum is one fifth the size of that in normal mice

behavior/neurological
• mice display ataxia that is characterized by frequent loss of balance, tremulous locomotion, tendency to drag hind limbs and hyperextension of the tail
• ataxic mice often display hyperextension of the tail




Genotype
MGI:3722181
ht4
Allelic
Composition
Dab1tm1Cpr/Dab1tm2Cpr
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dab1tm1Cpr mutation (1 available); any Dab1 mutation (77 available)
Dab1tm2Cpr mutation (0 available); any Dab1 mutation (77 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• authors state that mice exhibit the same ataxic phenotype as Dab1tm2Cpr homozygotes





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
04/30/2024
MGI 6.23
The Jackson Laboratory