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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mycbp2tm1.1Adia
targeted mutation 1.1, Aaron DiAntonio
MGI:3760640
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mycbp2tm1.1Adia/Mycbp2tm1.1Adia involves: C57BL/6 * FVB/N MGI:3760656
cx2
Ednrbs-15DttMb/Ednrb+
Mycbp2tm1.1Adia/Mycbp2+
involves: 101/Rl * C3H/Rl * C57BL/6 * FVB/N MGI:3760666
cx3
Map3k12Gt(RRN366)Byg/Map3k12Gt(RRN366)Byg
Mycbp2tm1.1Adia/Mycbp2tm1.1Adia
involves: 129P2/OlaHsd * C57BL/6 * FVB/N MGI:3760660


Genotype
MGI:3760656
hm1
Allelic
Composition
Mycbp2tm1.1Adia/Mycbp2tm1.1Adia
Genetic
Background
involves: C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mycbp2tm1.1Adia mutation (0 available); any Mycbp2 mutation (223 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die at birth without taking a breath

nervous system
• peripheral nerves are thin
• axons from the dorsal thalamus extend beyond their nuclei, avoiding the telencephalon and extending along the diencephalons-telecephalon boundary
• however, at E13.5 a well-formed domain of Islet1+ cells is present in the subcortical telencephalon indicating that the permissive corridor for migration into the telencephalon is present
• descending axons extend through the cerebral white matter and terminate abruptly at the border between the cortex and the striatum
• mice exhibit a general reduction in neurofilaments in the hippocampus, cerebral cortex, subcortical telencephalon and thalamus
• mice exhibit a reduction in staining for neurites of GABAnergic interneurons without a reduction in the number of GABAnergic cell bodies in the cerebral cortex
• the volume of lateral ventricles is increased and extends into the olfactory bulb
• the corpus callosum is reduced in size in the anterior-posterior and dorsal-ventral axes
• unlike in wild-type mice, corticofugal projections in the internal capsule contribute to the internal capsule
• mice lack the axonal tracts running through the internal capsule
• the interpeduncular fossa is exaggerated
• the diencephalon is small and altered in organization
• the habenulopeduncular tract is short
• the thalamus lacks innervation
• the lateral geniculate nucleus lacks innervation
• however, axons leave the retina, form an optic nerve and reach and cross the optic chiasm
• hippocampal formations are reduced in size and dysmorphic compared to in wild-type mice
• corticofugal and thalamocortical projections are lost
• by E18.5, corticofugal axons fail to exit the cerebral cortex and the thamamocortical axons fail to reach their targets in the cortex
• the thalamus lacks innervation
• motor neurons terminate normally but also extend dysmorphic extrasynaptic variscosities filled with axonal and synaptic markers
• the average motor unit size is increased relative to in wild-type mice with each motorneuron innervating more endplates than in wild-type mice
• mice have narrow phrenic nerves with fewer axons than in wild-type mice
• the ventral most region of the diaphragm often lacks innervation
• although post-synaptic endplate numbers in the diaphragm are normal, endplates are more densely packed within a narrower endplate band

muscle
• the ventral most region of the diaphragm often lacks innervation
• although post-synaptic endplate numbers in the diaphragm are normal, endplates are more densely packed within a narrower endplate band

cellular
• axons from the dorsal thalamus extend beyond their nuclei, avoiding the telencephalon and extending along the diencephalons-telecephalon boundary
• however, at E13.5 a well-formed domain of Islet1+ cells is present in the subcortical telencephalon indicating that the permissive corridor for migration into the telencephalon is present
• descending axons extend through the cerebral white matter and terminate abruptly at the border between the cortex and the striatum




Genotype
MGI:3760666
cx2
Allelic
Composition
Ednrbs-15DttMb/Ednrb+
Mycbp2tm1.1Adia/Mycbp2+
Genetic
Background
involves: 101/Rl * C3H/Rl * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ednrbs-15DttMb mutation (0 available); any Ednrb mutation (103 available)
Mycbp2tm1.1Adia mutation (0 available); any Mycbp2 mutation (223 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• authors state that mice exhibit the same gross morphological defects as observed in Phr1tm1.1Adia homozygotes




Genotype
MGI:3760660
cx3
Allelic
Composition
Map3k12Gt(RRN366)Byg/Map3k12Gt(RRN366)Byg
Mycbp2tm1.1Adia/Mycbp2tm1.1Adia
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map3k12Gt(RRN366)Byg mutation (1 available); any Map3k12 mutation (39 available)
Mycbp2tm1.1Adia mutation (0 available); any Mycbp2 mutation (223 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• authors state that mice exhibit the same gross morphological defects as observed in Phr1tm1.1Adia homozygotes
• lateral ventricles are increased in size
• mice lack the axon tract that runs through the internal capsule





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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory