Mn1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Mn1
meningioma 1
MGI:1261813

33 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Mn1^tm1Ecz/Mn1⁺ FVB.129-Mn1^tm1Ecz	abnormal cranial suture morphology	J:98889
	alisphenoid bone hypoplasia	J:98889
	basisphenoid bone hypoplasia	J:98889
	cleft secondary palate	J:98889
	large cranial foramen ovale	J:98889
	large foramen rotundum	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
Mn1^tm1Ecz/Mn1^tm1Ecz FVB.129-Mn1^tm1Ecz	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 temporal bone squamous part	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
	thin frontal bone	J:98889
	thin interparietal bone	J:98889
	thin parietal bone	J:98889

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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