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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Grpel1
GrpE-like 1, mitochondrial
MGI:1334417
10 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Grpel1tm1a(EUCOMM)Wtsi/Grpel1tm1a(EUCOMM)Wtsi
C57BL/6N-Grpel1tm1a(EUCOMM)Wtsi/Oulu
embryonic lethality, complete penetrance J:330869
Grpel1tm1c(EUCOMM)Wtsi/Grpel1tm1c(EUCOMM)Wtsi
Tg(ACTA1-cre/ERT2)97.16Mtz/0
involves: C57BL/6N
abnormal muscle physiology J:330869
abnormal skeletal muscle morphology J:330869
decreased circulating glucose level J:330869
decreased grip strength J:330869
decreased skeletal muscle fiber diameter J:330869
normal homeostasis/metabolism phenotype J:330869
skeletal muscle atrophy J:330869
skeletal muscle fibrosis J:330869
weight loss J:330869

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