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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ino80d
INO80 complex subunit D
MGI:3027003
8 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Ino80dtm1b(EUCOMM)Wtsi/Ino80d+
C57BL/6N-Ino80dtm1b(EUCOMM)Wtsi/Bay
abnormal retina outer nuclear layer morphology J:211773
decreased locomotor activity J:211773
decreased total body fat amount J:211773
decreased total retina thickness J:211773
increased lean body mass J:211773
Ino80dtm1b(EUCOMM)Wtsi/Ino80dtm1b(EUCOMM)Wtsi
C57BL/6N-Ino80dtm1b(EUCOMM)Wtsi/Bay
abnormal embryo size J:211773
embryonic growth retardation J:211773
preweaning lethality, incomplete penetrance 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
04/16/2024
MGI 6.23
The Jackson Laboratory