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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Apobec2
apolipoprotein B mRNA editing enzyme, catalytic polypeptide 2
MGI:1343178
12 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Apobec2Gt(OST259634)Lex/Apobec2Gt(OST259634)Lex
involves: 129S5/SvEvBrd * C57BL/6J
decreased body weight J:103485
decreased bone mineral content J:103485
decreased bone mineral density J:103485
postnatal growth retardation J:103485
Apobec2tm1Msn/Apobec2tm1Msn
B6.129P2-Apobec2tm1Msn
abnormal skeletal muscle fiber type ratio J:221028
abnormal soleus morphology J:221028
centrally nucleated skeletal muscle fibers J:221028
decreased body weight J:221028
decreased soleus weight J:221028
decreased tibialis anterior weight J:221028
increased variability of skeletal muscle fiber size J:221028
myopathy J:221028
Apobec2tm1Msn/Apobec2tm1Msn
involves: 129P2/OlaHsd * C57BL/6
no abnormal phenotype detected J:119326

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