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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Braftm1(ARAF)Urr
targeted mutation 1, Ulf R Rapp
MGI:3664469
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Braftm1(ARAF)Urr/Braftm1(ARAF)Urr involves: 129S1/Sv * C57BL/6 MGI:3710367
hm2
Braftm1(ARAF)Urr/Braftm1(ARAF)Urr involves: 129S1/Sv * C57BL/6 * CD-1 MGI:3710368


Genotype
MGI:3710367
hm1
Allelic
Composition
Braftm1(ARAF)Urr/Braftm1(ARAF)Urr
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1(ARAF)Urr mutation (0 available); any Braf mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• Background Sensitivity: while embryos survive passed E12.5 in a B6 background, less than one third of mice survive passed E13.5

cellular
• endothelial cells undergo increased apoptosis compared to controls or Braftm1(ARAF)Urr homozygotes




Genotype
MGI:3710368
hm2
Allelic
Composition
Braftm1(ARAF)Urr/Braftm1(ARAF)Urr
Genetic
Background
involves: 129S1/Sv * C57BL/6 * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Braftm1(ARAF)Urr mutation (0 available); any Braf mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all mice are dead by 8 weeks postnatal
• Background Sensitivity: in a mixed B6/CD-1 background, more embryos survive than on a B6 background, but only one third survive passed E13.5 and very few survive until 8 weeks postnatal

growth/size/body
• embryos found between E13.5 and E16.5 are small but morphologically normal
• embryos have reduced body weight by about two-fold
• however, no visible behavioral or developmental defects are observed and all organ weights are proportional with the exception of the thymus and spleen

nervous system
• at E14.5, the cortical plate has threefold fewer migrating late born neurons and in a Boyden transwell assay cortical neurons fail to migrate in response to BDNF
• however, alignment and density of radial glial cells and the number of Cajal-Retzius neurons expressing Reelin are normal
• at E14.5 and E16.5, there is a decrease in cortical progenitor cell proliferation in the ventricular zone
• at E16.5, the distance between the subplate and the plial surface is reduced nearly two-fold (from 246um in controls to 127um) but the cortex width is reduced by only 16% (from 592um in controls to 497um in homozygotes)
• at E16.5, the clear boundary between the subplate and the intermediate zone, in which many neurons (TBB1+) are abnormally present, is not visible and cell density in the subplate and the intermediate zone is increased
• at E18.5, Pou3f2+ cells are located deeper in the cortical plate than in wild-type mice
• at P19, neuronal cell bodies are small, round and nearly completely lack the pyramidal cell marker Pou3f2+ in the somatosensory and visual cortexes
• at P19, the more anterior cortex has reduced pyramidal cell marker expression (Pou3f2+)
• at P19, the somatosensory cortex thickness is reduced in layers II, III and V
• however, there is an increase in cell number in layer IV
• at P19, neuronal cells nearly completely lack the pyramidal cell marker Pou3f2
• at P19, mature neurons (NEUN+) are tightly packed in layers II and III unlike in wild-type
• at P19, the apical cortical dendrites (MAP2+) of layer II to V are unfasciculated and disorganized as determined
• at P19, neuronal cells nearly completely lack the pyramidal cell marker Pou3f2
• at P19, the somatosensory cortex thickness is reduced in layers II, III and V
• however, there is an increase in cell number in layer IV

hematopoietic system
• 10-fold lower
• 10-fold lower

embryo
• embryos found between E13.5 and E16.5 are small but morphologically normal

immune system
• 10-fold lower
• 10-fold lower

endocrine/exocrine glands
• 10-fold lower





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
04/23/2024
MGI 6.23
The Jackson Laboratory