Symbol Name ID |
Men1
multiple endocrine neoplasia 1 MGI:1316736 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Increased susceptibility to fractures |
Chondrocalcinosis |
Back pain |
Reduced bone mineral density |
Osteopenia |
Generalized osteoporosis |
Osteolysis |
Disease(s) Associated with MEN1 | |||||||
hyperparathyroidism | |||||||
multiple endocrine neoplasia type 1 | |||||||
pancreatic cancer |
Mouse Phenotypes | skeleton phenotype |
abnormal basisphenoid bone morphology |
abnormal pterygoid process morphology |
abnormal sternum morphology |
abnormal sternum ossification |
abnormal rib morphology |
abnormal rib development |
rib bifurcation |
rib fusion |
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Availability | Mouse Genotype | |||||||||
Men1tm1.2Ctre/Men1tm1.2Ctre Pax3tm1(cre)Joe/Pax3+ (conditional) |
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Men1tm1.2Ctre/Men1tm1.2Ctre Tg(Pax3-cre)1Joe/0 (conditional) |
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Men1tm1.2Ctre/Men1tm1.2Ctre H2az2Tg(Wnt1-cre)11Rth/H2az2+ (conditional) |
* |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 05/14/2024 MGI 6.23 |
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