- hypoglycemia / MGI
- increased circulating calcium level / MGI
- decreased circulating phosphate level / MGI
- thin ventricular wall / MGI
- trabecula carnea hypoplasia / MGI
- delayed hepatic development / MGI
- abnormal pituitary gland morphology / MGI
- enlarged pituitary gland / MGI
- enlarged adrenal glands / MGI
- exencephaly / MGI
- enlarged testis / MGI
- Leydig cell hyperplasia / MGI
- decreased embryo size / MGI
- increased circulating corticosterone level / MGI
- pancreas inflammation / MGI
- hemorrhage / MGI
- abnormal pancreas morphology / MGI
- increased tumor incidence / MGI
- increased lung adenocarcinoma incidence / MGI
- increased adrenal gland tumor incidence / MGI
- increased carcinoma incidence / MGI
- increased pituitary adenoma incidence / MGI
- increased pheochromocytoma incidence / MGI
- increased circulating insulin level / MGI
- premature death / MGI
- abnormal embryonic tissue morphology / MGI
- increased intestinal adenoma incidence / MGI
- pancreas cysts / MGI
- increased insulinoma incidence / MGI
- increased glucagonoma incidence / MGI
- increased pancreatic islet cell adenoma incidence / MGI
- parathyroid gland hyperplasia / MGI
- increased parathyroid adenoma incidence / MGI
- increased thyroid adenoma incidence / MGI
- thyroid gland hyperplasia / MGI
- increased prolactinoma incidence / MGI
- increased pancreatic beta cell number / MGI
- abnormal neural tube closure / MGI
- abnormal craniofacial development / MGI
- embryonic growth retardation / MGI
- enlarged ovary / MGI
- abnormal cell differentiation / MGI
- homeostasis/metabolism phenotype / MGI
- pancreatic islet hyperplasia / MGI
- increased testis tumor incidence / MGI
- increased ovary tumor incidence / MGI
- increased lung tumor incidence / MGI
- increased pancreas adenoma incidence / MGI
- increased adrenal gland adenoma incidence / MGI
- abnormal pancreatic acinar cell morphology / MGI
- pancreas necrosis / MGI
- increased pancreas tumor incidence / MGI
- increased gonad tumor incidence / MGI
- increased Leydig cell tumor incidence / MGI
- increased gastrointestinal tumor incidence / MGI
- increased gland tumor incidence / MGI
- increased mammary gland tumor incidence / MGI
- increased stomach tumor incidence / MGI
- increased thyroid tumor incidence / MGI
- increased pituitary gland tumor incidence / MGI
- increased parathyroid gland tumor incidence / MGI
- increased thyroid carcinoma incidence / MGI
- increased pancreatic islet cell carcinoma incidence / MGI
- increased pituitary adenohypophysis tumor incidence / MGI
- increased adrenal cortical tumor incidence / MGI
- increased adrenocortical adenoma incidence / MGI
- thin interventricular septum / MGI
- embryonic lethality, complete penetrance / MGI
- embryonic lethality during organogenesis, complete penetrance / MGI
- lethality throughout fetal growth and development, complete penetrance / MGI
- thyroid cyst / MGI
STOCK Men1tm1.2Zqw/Flmg
Status | Available to order |
EMMA ID | EM:09502 |
Citation information | RRID:IMSR_EM:09502 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 | STOCK Men1tm1.2Zqw/Flmg |
Alternative name | Men1floxed/floxed |
Strain type | Targeted Mutant Strains : Conditional mutation |
Allele/Transgene symbol | Men1tm1.2Zqw |
Gene/Transgene symbol | Men1 |
Information from provider
Provider | Philippe Bertolino |
Provider affiliation | Cancer Research Center of Lyon |
Genetic information | Mice carrying the homozygous floxed Men1 allele. |
Phenotypic information | Homozygous:No phenotype has been observed.Heterozygous:No phenotype has been observed. |
References |
|
Homozygous fertile | yes |
Homozygous viable | yes |
Homozygous matings required | no |
Immunocompromised | no |
Information from EMMA
Archiving centre | B.S.R.C. Alexander Fleming, Vari, Greece |
Animals used for archiving | homozygous mixed 129, C57BL/6 males, wild-type C57BL/6J females |
Stage of embryos | Morula |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Pituitary gigantism / Orphanet_99725
- Familial isolated hyperparathyroidism / Orphanet_99879
- Multiple endocrine neoplasia type 1 / Orphanet_652
MGI phenotypes (gene matching)
Literature references
- Genetic ablation of the tumor suppressor menin causes lethality at mid-gestation with defects in multiple organs.;Bertolino Philippe, Radovanovic Ivan, Casse Huguette, Aguzzi Adriano, Wang Zhao-Qi, Zhang Chang-Xian, ;2003;Mechanisms of development;120;549-60; 12782272
- Pancreatic beta-cell-specific ablation of the multiple endocrine neoplasia type 1 (MEN1) gene causes full penetrance of insulinoma development in mice.;Bertolino Philippe, Tong Wei-Min, Herrera Pedro Luis, Casse Huguette, Zhang Chang Xian, Wang Zhao-Qi, ;2003;Cancer research;63;4836-41; 12941803
- Alpha cell-specific Men1 ablation triggers the transdifferentiation of glucagon-expressing cells and insulinoma development.;Lu Jieli, Herrera Pedro L, Carreira Christine, Bonnavion Rémy, Seigne Christelle, Calender Alain, Bertolino Philippe, Zhang Chang Xian, ;2010;Gastroenterology;138;1954-65; 20138042
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