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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Map1btm1Prop
targeted mutation 1, Friedrich Propst
MGI:3575407
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Map1btm1Prop/Map1btm1Prop involves: 129S1/Sv * 129X1/SvJ MGI:3575572
hm2
Map1btm1Prop/Map1btm1Prop involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:3575571
cx3
Kif21atm1.1Ece/Kif21a+
Map1btm1Prop/Map1b+
Tg(Isl1-EGFP*)1Slp/0
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/c * C57BL/6 MGI:6241441
cx4
Map1btm1Prop/Map1btm1Prop
Tg(Isl1-EGFP*)1Slp/0
involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 MGI:6241439


Genotype
MGI:3575572
hm1
Allelic
Composition
Map1btm1Prop/Map1btm1Prop
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map1btm1Prop mutation (0 available); any Map1b mutation (85 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
vision/eye
• mice exhibit unilateral or bilateral ptosis and/or globe retraction that is 90% penetrant
• mice exhibit unilateral or bilateral ptosis and/or globe retraction that is 90% penetrant

nervous system
• in dorsal root ganglia explants axon outgrowth is wavy/frizzy and covers less area
• dissociated dorsal root ganglion neurons display a curled aspect, have more branching points per neurite, and are more likely to stop growing rather than turn away from a nonpermissive area

cellular
• in dorsal root ganglia explants axon outgrowth is wavy/frizzy and covers less area
• dissociated dorsal root ganglion neurons display a curled aspect, have more branching points per neurite, and are more likely to stop growing rather than turn away from a nonpermissive area




Genotype
MGI:3575571
hm2
Allelic
Composition
Map1btm1Prop/Map1btm1Prop
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map1btm1Prop mutation (0 available); any Map1b mutation (85 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• about 56% of homozygous pups die postnatally

behavior/neurological
• exploratory activity is absent; however, general activity and gait are normal

growth/size/body
• severely reduced body weight is seen in 94% of homozygous pups
• this body weight reduction is most pronounced before weaning and is decreased later in life through the loss of the most severely affected pups

homeostasis/metabolism
• homozygotes appear dehydrated and malnourished

reproductive system
• homozygotes are poor breeders

vision/eye
• in 94% of homozygotes one or both eyes appear smaller or retracted; however, eyeball size is normal
• retinal morphology is normal

nervous system
• in 20% of homozygotes the corpus callosum is thin throughout the brain or absent only in the posterior portions of the forebrain
• in 80% of homozygotes agenesis of the corpus callosum is seen
• in the parietal portion of the brain the corpus callosum is replaced by a fine fibrous membrane containing the choroid plexus of the third ventricle
• a longitudinal bundle of myelinated fibers (similar to a Probst bundle) is found in the most medial aspects of the white matter
• the cingulate gyrus is rotated ventrally
• the hippocampus is dislocated laterally; however, the cortical architecture is normal
• aberrant bundles of myelinated axons are found in the deeper layers of the parietal cortex
• in the peripheral nerves the number of axons in the intermediate and large size classes are decreased and myelin sheaths of axons within a given size class are thinner; however the overall number of axons is normal
• in the peripheral nerves myelin sheaths of axons within a given size class are thinner
• motor nerve conduction velocity is reduced to 19.82 +/- 2.93 compared to 30.60 +/- 6.71 in wild-type mice

integument




Genotype
MGI:6241441
cx3
Allelic
Composition
Kif21atm1.1Ece/Kif21a+
Map1btm1Prop/Map1b+
Tg(Isl1-EGFP*)1Slp/0
Genetic
Background
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kif21atm1.1Ece mutation (0 available); any Kif21a mutation (81 available)
Map1btm1Prop mutation (0 available); any Map1b mutation (85 available)
Tg(Isl1-EGFP*)1Slp mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• approximately 90% penetrance of abducens nerve hypoplasia
• oculomotor nerve superior branch axons terminate prematurely within a bulb with a penetrance of 90%




Genotype
MGI:6241439
cx4
Allelic
Composition
Map1btm1Prop/Map1btm1Prop
Tg(Isl1-EGFP*)1Slp/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Map1btm1Prop mutation (0 available); any Map1b mutation (85 available)
Tg(Isl1-EGFP*)1Slp mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• 90% of oculomotor nerves have mild proximal thickening in the absence of a bulb, distal thinning, hypoplasia of the oculomotor nerve superior division and a smaller oculomotor nerve inferior division
• about 30% of distal oculomotor nerves have aberrant, long, fasciculated branches that emerge from the oculomotor nerve inferior division exploratory region





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last database update
07/05/2024
MGI 6.24
The Jackson Laboratory