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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Apbb2
amyloid beta precursor protein binding family B member 2
MGI:108405
10 phenotypes from 4 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Apbb2M1Btlr/Apbb2M1Btlr
C57BL/6J-Apbb2M1Btlr
impaired glucose tolerance J:265064
Apbb2m2Btlr/Apbb2m2Btlr
C57BL/6J-Apbb2m2Btlr
impaired glucose tolerance J:265072
Apbb2tm1.1(KOMP)Vlcg/Apbb2+
C57BL/6N-Apbb2tm1.1(KOMP)Vlcg/Ucd
abnormal eye morphology J:211773
abnormal skin morphology J:211773
hemorrhage J:211773
increased circulating alanine transaminase level J:211773
increased circulating aspartate transaminase level J:211773
increased lung weight J:211773
spina bifida J:211773
Apbb2tm1.1(KOMP)Vlcg/Apbb2tm1.1(KOMP)Vlcg
C57BL/6N-Apbb2tm1.1(KOMP)Vlcg/Ucd
hemorrhage J:211773
preweaning lethality, incomplete penetrance J:211773
spina bifida J:211773
Apbb2tm1Her/Apbb2tm1Her
involves: 129S6/SvEvTac * C57BL/6
no abnormal phenotype detected J:105160

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
11/12/2024
MGI 6.24
The Jackson Laboratory