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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fndc5
fibronectin type III domain containing 5
MGI:1917614
17 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Fndc5em21Gpt/Fndc5em21Gpt
C57BL/6JGpt-Fndc5em21Cd/Gpt
abnormal behavior J:247171
abnormal circulating enzyme level J:247171
abnormal circulating lipid level J:247171
abnormal fatty acid oxidation J:247171
normal growth/size/body region phenotype J:247171
impaired autophagy J:247171
increased susceptibility to diet-induced hepatic steatosis J:247171
increased susceptibility to diet-induced obesity J:247171, J:291193
increased susceptibility to hepatic steatosis J:247171
increased susceptibility to induced morbidity/mortality J:291193
Fndc5tm1.1Brsp/Fndc5tm1.1Brsp
involves: C57BL/6J
abnormal osteocyte lacuna morphology J:269575
abnormal osteocyte morphology J:269575
decreased bone resorption J:269575
decreased susceptibility to osteoporosis J:269575
increased trabecular bone connectivity density J:269575
increased trabecular bone mass J:269575
normal skeleton phenotype J:269575

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
04/23/2024
MGI 6.23
The Jackson Laboratory