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Symbol
Name
ID
Men1
multiple endocrine neoplasia 1
MGI:1316736
Phenotype annotations related to craniofacial
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
Availability Mouse Genotype
Men1tm1Ctre/Men1tm1Ctre
Men1tm1.2Ctre/Men1tm1.2Ctre
Pax3tm1(cre)Joe/Pax3+  (conditional)
Men1tm1.2Ctre/Men1tm1.2Ctre
Tg(Pax3-cre)1Joe/0  (conditional)
Men1tm1.2Ctre/Men1tm1.2Ctre
H2az2Tg(Wnt1-cre)11Rth/H2az2+  (conditional)

Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory