Symbol Name ID |
Men1
multiple endocrine neoplasia 1 MGI:1316736 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormality of the head |
Adenoma sebaceum |
Gingival fibromatosis |
Disease(s) Associated with MEN1 | |||
hyperparathyroidism | |||
multiple endocrine neoplasia type 1 |
Mouse Phenotypes | abnormal basisphenoid bone morphology |
abnormal pterygoid process morphology |
abnormal craniofacial development |
abnormal palatal mesenchymal cell differentiation |
abnormal palatal mesenchymal cell proliferation |
abnormal secondary palate development |
abnormal palatal shelf bone ossification |
palatal shelves fail to meet at midline |
palatal shelf hypoplasia |
short soft palate |
cleft secondary palate |
bilateral cleft palate |
abnormal snout morphology |
short snout |
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Availability | Mouse Genotype | ||||||||||||||
Men1tm1Ctre/Men1tm1Ctre | |||||||||||||||
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 07/05/2024 MGI 6.24 |
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