- abnormal aorta morphology / MGI
- abnormal head morphology / MGI
- abnormal blood vessel morphology / MGI
- poor circulation / MGI
- abnormal apoptosis / MGI
- hemorrhage / MGI
- intraventricular hemorrhage / MGI
- abnormal neuron morphology / MGI
- abnormal vitelline vasculature morphology / MGI
- abnormal cardinal vein morphology / MGI
- hemopericardium / MGI
- decreased heart rate / MGI
- abnormal vascular endothelial cell morphology / MGI
- increased vascular endothelial cell number / MGI
- hematoma / MGI
- decreased embryo weight / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- abnormal telencephalon development / MGI
B6.129-Braftm1Zim/Cnrm
Status | Available to order |
EMMA ID | EM:01389 |
Citation information | RRID:IMSR_EM:01389 Research Resource Identifiers (RRID) are persistent unique ID numbers assigned to help researchers cite key resources (e.g. antibodies, model organisms and software projects) in the biomedical literature to improve transparency and reproducibility in research. See https://www.rrids.org/ for more information. |
International strain name | B6.129-Braftm1Zim/Cnrm |
Alternative name | Braf Knock-out |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Braftm1Zim |
Gene/Transgene symbol | Braf |
Information from provider
Provider | Leszek Wojnowski |
Provider affiliation | University Mainz |
Genetic information | See Wojnowski et al., Endothelial apoptosis in Braf-deficient mice. Nature Genetics, 16: 293-297 (1997) |
Phenotypic information | Mid-gestational lethality, due to defective angiogenesis. |
References |
|
Information from EMMA
Archiving centre | CNR, Consiglio Nazionale delle Ricerche, Monterotondo, Italy |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Pilomyxoid astrocytoma / Orphanet_251615
- Classic hairy cell leukemia / Orphanet_58017
- Craniopharyngioma / Orphanet_54595
- Differentiated thyroid carcinoma / Orphanet_146
- Langerhans cell histiocytosis / Orphanet_389
- Cardiofaciocutaneous syndrome / Orphanet_1340
- Noonan syndrome with multiple lentigines / Orphanet_500
- Syringocystadenoma papilliferum / Orphanet_840
MGI phenotypes (allele matching)
MGI phenotypes (gene matching)
- abnormal neurocranium morphology / MGI
- abnormal frontal bone morphology / MGI
- abnormal parietal bone morphology / MGI
- abnormal aorta morphology / MGI
- enlarged heart / MGI
- heart hyperplasia / MGI
- abnormal cell morphology / MGI
- abnormal head morphology / MGI
- shortened head / MGI
- abnormal thymus morphology / MGI
- decreased thymocyte number / MGI
- abnormal stratification in cerebral cortex / MGI
- abnormal visual cortex morphology / MGI
- abnormal somatosensory cortex morphology / MGI
- abnormal telencephalon development / MGI
- convulsive seizures / MGI
- decreased body weight / MGI
- decreased body size / MGI
- increased metastatic potential / MGI
- cataract / MGI
- abnormal mating frequency / MGI
- hyperactivity / MGI
- abnormal blood vessel morphology / MGI
- poor circulation / MGI
- abnormal apoptosis / MGI
- decreased embryo size / MGI
- abnormal placenta morphology / MGI
- abnormal placenta labyrinth morphology / MGI
- decreased white adipose tissue amount / MGI
- abnormal immune system physiology / MGI
- hemorrhage / MGI
- intraventricular hemorrhage / MGI
- increased lung adenoma incidence / MGI
- increased pheochromocytoma incidence / MGI
- premature death / MGI
- abnormal kidney morphology / MGI
- no abnormal phenotype detected / MGI
- abnormal astrocyte morphology / MGI
- abnormal long term object recognition memory / MGI
- abnormal neuron morphology / MGI
- increased neuron apoptosis / MGI
- abnormal vitelline vasculature morphology / MGI
- oliguria / MGI
- thymus atrophy / MGI
- embryonic growth retardation / MGI
- abnormal spongiotrophoblast layer morphology / MGI
- small placenta / MGI
- abnormal cardinal vein morphology / MGI
- decreased spleen weight / MGI
- decreased thymus weight / MGI
- abnormal trophoblast layer morphology / MGI
- hemopericardium / MGI
- decreased heart rate / MGI
- behavior/neurological phenotype / MGI
- tachypnea / MGI
- decreased creatinine clearance / MGI
- increased cardiac muscle contractility / MGI
- increased circulating noradrenaline level / MGI
- increased apoptosis / MGI
- abnormal vascular endothelial cell morphology / MGI
- increased vascular endothelial cell number / MGI
- thin cerebral cortex / MGI
- abnormal placental labyrinth vasculature morphology / MGI
- hematoma / MGI
- abnormal pancreatic acinar cell morphology / MGI
- increased splenocyte apoptosis / MGI
- abnormal dermal melanocyte morphology / MGI
- decreased embryo weight / MGI
- abnormal skin sebaceous gland morphology / MGI
- increased thymocyte apoptosis / MGI
- abnormal cerebral cortex pyramidal cell morphology / MGI
- abnormal basicranium morphology / MGI
- increased gland tumor incidence / MGI
- postnatal lethality, incomplete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- embryonic lethality during organogenesis, incomplete penetrance / MGI
- round head / MGI
Literature references
- Endothelial apoptosis in Braf-deficient mice.;Wojnowski L, Zimmer A M, Beck T W, Hahn H, Bernal R, Rapp U R, Zimmer A, ;1997;Nature genetics;16;293-7; 9207797
- Overlapping and specific functions of Braf and Craf-1 proto-oncogenes during mouse embryogenesis.;Wojnowski L, Stancato L F, Larner A C, Rapp U R, Zimmer A, ;2000;Mechanisms of development;91;97-104; 10704835
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