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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Mn1
meningioma 1
MGI:1261813
28 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Mn1tm1Ecz/Mn1+
FVB.129-Mn1tm1Ecz
abnormal cranial suture morphology J:98889
alisphenoid bone hypoplasia J:98889
basisphenoid bone hypoplasia J:98889
cleft secondary palate J:98889
neonatal lethality, incomplete penetrance J:98889
normal neoplasm J:98889
palate bone hypoplasia J:98889
presphenoid bone hypoplasia J:98889
pterygoid bone hypoplasia J:98889
temporal bone hypoplasia J:98889
vomer bone hypoplasia J:98889
Mn1tm1Ecz/Mn1tm1Ecz
FVB.129-Mn1tm1Ecz
abnormal frontal bone morphology J:98889
abnormal interparietal bone morphology J:98889
abnormal parietal bone morphology J:98889
abnormal pterygoid process morphology J:98889
abnormal sphenoid bone morphology J:98889
abnormal suckling behavior J:98889
abnormal supraoccipital bone morphology J:98889
absent alisphenoid bone J:98889
absent squamosal bone J:98889
absent vomer bone J:98889
basisphenoid bone hypoplasia J:98889
cleft secondary palate J:98889
cyanosis J:98889
lethargy J:98889
maxillary shelf hypoplasia J:98889
palatal shelves fail to meet at midline J:98889
palatine bone horizontal plate hypoplasia J:98889
perinatal lethality, complete penetrance J:98889
presphenoid bone hypoplasia J:98889
respiratory distress J:98889

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
10/10/2017
MGI 6.10
The Jackson Laboratory