- kyphosis / MGI
- abnormal cartilage morphology / MGI
- abnormal erythropoiesis / MGI
- abnormal cell proliferation / MGI
- increased cell proliferation / MGI
- abnormal liver morphology / MGI
- liver hypoplasia / MGI
- small liver / MGI
- enlarged liver sinusoidal spaces / MGI
- decreased hepatocyte number / MGI
- abnormal hepatocyte morphology / MGI
- mammary gland hyperplasia / MGI
- abnormal neuroendocrine gland morphology / MGI
- decreased brain size / MGI
- abnormal frontal lobe morphology / MGI
- abnormal third ventricle morphology / MGI
- abnormal fourth ventricle morphology / MGI
- dilated fourth ventricle / MGI
- abnormal Purkinje cell morphology / MGI
- ectopic Purkinje cell / MGI
- abnormal dorsal root ganglion morphology / MGI
- small dorsal root ganglion / MGI
- abnormal trigeminal ganglion morphology / MGI
- obese / MGI
- increased metastatic potential / MGI
- cataract / MGI
- abnormal pilomotor reflex / MGI
- hunched posture / MGI
- anemia / MGI
- abnormal myelopoiesis / MGI
- abnormal blood vessel morphology / MGI
- abnormal embryo development / MGI
- decreased embryo size / MGI
- abnormal placenta labyrinth morphology / MGI
- pale yolk sac / MGI
- edema / MGI
- skin edema / MGI
- pericardial edema / MGI
- mammary gland duct hyperplasia / MGI
- respiratory distress / MGI
- neoplasm / MGI
- preneoplasia / MGI
- increased tumor incidence / MGI
- increased pituitary adenoma incidence / MGI
- increased pheochromocytoma incidence / MGI
- premature death / MGI
- abnormal definitive hematopoiesis / MGI
- abnormal brain morphology / MGI
- no abnormal phenotype detected / MGI
- neurodegeneration / MGI
- abnormal macrophage morphology / MGI
- abnormal erythrocyte morphology / MGI
- low mean erythrocyte cell number / MGI
- abnormal lens fiber morphology / MGI
- decreased erythrocyte cell number / MGI
- no phenotypic analysis / MGI
- abnormal cell cycle / MGI
- increased neuron apoptosis / MGI
- nervous system phenotype / MGI
- abnormal response/metabolism to endogenous compounds / MGI
- abnormal chromosome morphology / MGI
- pallor / MGI
- abnormal milk ejection / MGI
- embryonic growth retardation / MGI
- aneuploidy / MGI
- abnormal cell cycle checkpoint function / MGI
- abnormal mitosis / MGI
- decreased fetal size / MGI
- abnormal placental transport / MGI
- hypoxia / MGI
- abnormal cell differentiation / MGI
- cachexia / MGI
- lethargy / MGI
- digestive/alimentary phenotype / MGI
- cellular phenotype / MGI
- vision/eye phenotype / MGI
- abnormal lens development / MGI
- increased apoptosis / MGI
- decreased apoptosis / MGI
- abnormal retinal apoptosis / MGI
- increased body mass index / MGI
- thin cerebellar granule layer / MGI
- increased lung tumor incidence / MGI
- abnormal macrophage differentiation / MGI
- increased megakaryocyte cell number / MGI
- enlarged fourth ventricle / MGI
- increased lens fiber apoptosis / MGI
- increased brain tumor incidence / MGI
- increased nucleated erythrocyte cell number / MGI
- skeletal muscle atrophy / MGI
- increased sensitivity to induced morbidity/mortality / MGI
- decreased sensitivity to induced morbidity/mortality / MGI
- abnormal neuron differentiation / MGI
- increased thyroid tumor incidence / MGI
- increased pituitary gland tumor incidence / MGI
- increased thyroid C-cell carcinoma incidence / MGI
- increased pituitary adenohypophysis tumor incidence / MGI
- increased pituitary melanotroph tumor incidence / MGI
- postnatal lethality, incomplete penetrance / MGI
- neonatal lethality, incomplete penetrance / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- preweaning lethality, incomplete penetrance / MGI
- increased fibroblast proliferation / MGI
- decreased retinal apoptosis / MGI
- flat forehead / MGI
FVB;129P2-Rb1tm2Brn/Cnrm
Status | Available to order |
EMMA ID | EM:00433 |
Citation information | RRID:IMSR_EM:00433 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 | FVB;129P2-Rb1tm2Brn/Cnrm |
Alternative name | RbF |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Rb1tm2Brn |
Gene/Transgene symbol | Rb1 |
Information from provider
Provider | Anton Berns |
Provider affiliation | Research - Animal Facility, The Netherlands Cancer Institute |
Genetic information | Insertion of loxP sequences into the introns surrounding exon 19 of the Rb1 gene. |
Phenotypic information | Conditional Rb1 knock-out; no phenotype. |
References |
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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
- Small cell lung cancer / Orphanet_70573
- Non-hereditary retinoblastoma / Orphanet_357034
- Hereditary retinoblastoma / Orphanet_357027
MGI phenotypes (gene matching)
Literature references
- Induction of medulloblastomas in p53-null mutant mice by somatic inactivation of Rb in the external granular layer cells of the cerebellum.;Marino S, Vooijs M, van Der Gulden H, Jonkers J, Berns A, ;2000;Genes & development;14;994-1004; 10783170
Information on how we integrate external resources can be found here
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