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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Bnc2
basonuclin 2
MGI:2443805
19 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Bnc2Gt(pU21)18Imeg/Bnc2Gt(pU21)18Imeg
involves: C57BL/6 * CBA
abnormal maxillary shelf morphology J:151992
abnormal palate development J:151992
abnormal pterygoid process morphology J:151992
absent palatine bone J:151992
cleft secondary palate J:151992
decreased birth body size J:151992
decreased tongue size J:151992
frontal bone hypoplasia J:151992
large posterior fontanelle J:151992
meteorism J:151992
microcephaly J:151992
neonatal lethality, complete penetrance J:151992
palatal shelves fail to meet at midline J:151992
parietal bone hypoplasia J:151992
small alisphenoid bone J:151992
wide sagittal suture J:151992
Bnc2tm1b(KOMP)Wtsi/Bnc2+
C57BL/6N-Bnc2tm1b(KOMP)Wtsi/Orl
decreased exploration in new environment J:211773
increased cornea thickness J:211773
increased prepulse inhibition J:211773

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
02/23/2021
MGI 6.16
The Jackson Laboratory