- abnormal heart development / MGI
- abnormal cell death / MGI
- decreased cell proliferation / MGI
- abnormal hair follicle morphology / MGI
- decreased hair follicle number / MGI
- abnormal awl hair morphology / MGI
- kinked tail / MGI
- abnormal mammary gland morphology / MGI
- abnormal mammary gland development / MGI
- mammary gland hyperplasia / MGI
- abnormal branching of the mammary ductal tree / MGI
- abnormal embryonic neuroepithelial layer differentiation / MGI
- exencephaly / MGI
- open neural tube / MGI
- abnormal ovary morphology / MGI
- abnormal uterine cervix squamous epithelium morphology / MGI
- small testis / MGI
- arrest of spermatogenesis / MGI
- dermatitis / MGI
- increased body weight / MGI
- decreased body weight / MGI
- hyperactivity / MGI
- increased mortality induced by gamma-irradiation / MGI
- absent mesoderm / MGI
- abnormal axial mesoderm / MGI
- incomplete somite formation / MGI
- failure of primitive streak formation / MGI
- absent egg cylinders / MGI
- decreased embryo size / MGI
- absent amniotic folds / MGI
- absent trophoblast giant cells / MGI
- postnatal growth retardation / MGI
- mammary gland duct hyperplasia / MGI
- male infertility / MGI
- neoplasm / MGI
- increased cellular sensitivity to gamma-irradiation / MGI
- increased tumor incidence / MGI
- increased T cell derived lymphoma incidence / MGI
- abnormal hair growth / MGI
- abnormal coat/hair pigmentation / MGI
- abnormal developmental patterning / MGI
- abnormal embryonic tissue morphology / MGI
- abnormal extraembryonic tissue morphology / MGI
- abnormal skin pigmentation / MGI
- no abnormal phenotype detected / MGI
- abnormal primitive streak formation / MGI
- disorganized extraembryonic tissue / MGI
- uterus hyperplasia / MGI
- spina bifida / MGI
- abnormal cell cycle / MGI
- abnormal egg cylinder morphology / MGI
- abnormal cell migration / MGI
- abnormal cell nucleus morphology / MGI
- enlarged tail bud / MGI
- abnormal cell adhesion / MGI
- abnormal nervous system morphology / MGI
- abnormal embryonic-extraembryonic boundary morphology / MGI
- embryonic growth retardation / MGI
- disorganized embryonic tissue / MGI
- abnormal chromosome number / MGI
- increased incidence of tumors by ionizing radiation induction / MGI
- abnormal trophoblast layer morphology / MGI
- azoospermia / MGI
- cellular phenotype / MGI
- reproductive system phenotype / MGI
- increased apoptosis / MGI
- early cellular replicative senescence / MGI
- increased liver tumor incidence / MGI
- abnormal small intestinal villus morphology / MGI
- decreased survivor rate / MGI
- decreased subcutaneous adipose tissue amount / MGI
- endometrium hyperplasia / MGI
- abnormal mammary gland duct morphology / MGI
- abnormal mammary gland epithelium morphology / MGI
- abnormal mammary gland lobule morphology / MGI
- increased mammary gland ductal carcinoma incidence / MGI
- empty decidua capsularis / MGI
- abnormal mitotic spindle morphology / MGI
- increased sensitivity to xenobiotic induced morbidity/mortality / MGI
- increased mammary gland epithelial cell proliferation / MGI
- decreased mammary gland epithelial cell proliferation / MGI
- increased hepatoma incidence / MGI
- increased mammary gland tumor incidence / MGI
- increased lipoma incidence / MGI
- mortality/aging / MGI
- abnormal double-strand DNA break repair / MGI
- prenatal lethality, complete penetrance / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality between implantation and placentation, complete penetrance / MGI
- embryonic lethality between implantation and somite formation, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- prenatal lethality, incomplete penetrance / MGI
- abnormal visceral endoderm morphology / MGI
- abnormal parietal endoderm morphology / MGI
- decreased fibroblast proliferation / MGI
- increased lymphoma incidence / MGI
- decreased small intestinal villus height / MGI
- increased mammary gland apoptosis / MGI
FVB.129P2-Brca1tm1Brn/Cnrm
Status | Available to order |
EMMA ID | EM:01645 |
Citation information | RRID:IMSR_EM:01645 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-Brca1tm1Brn/Cnrm |
Alternative name | Br1F |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Brca1tm1Brn |
Gene/Transgene symbol | Brca1 |
Information from provider
Provider | Anton Berns |
Provider affiliation | Research - Animal Facility, The Netherlands Cancer Institute |
Genetic information | Insertion of 5' (intron 4) and 3' (intron 13) loxP sites in the Brca1 gene, by homologous recombination in ES cells. |
Phenotypic information | None. |
Breeding history | 6 generations backcrossed on FVB/N. |
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
- Fanconi anemia / Orphanet_84
- Hereditary breast and ovarian cancer syndrome / Orphanet_145
- Cholangiocarcinoma / Orphanet_70567
MGI phenotypes (gene matching)
Literature references
- Conditional inactivation of Brca1 in the mouse ovarian surface epithelium results in an increase in preneoplastic changes.;Clark-Knowles Katherine V, Garson Kenneth, Jonkers Jos, Vanderhyden Barbara C, ;2007;Experimental cell research;313;133-45; 17070800
Information on how we integrate external resources can be found here
INFRAFRONTIER® and European Mouse Mutant Archive - EMMA® are registered trademarks at the European Union Intellectual Property Office (EUIPO).