- 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 |
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, wild-type C57BL/6J |
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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