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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Myo3b
myosin IIIB
MGI:2448580
7 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background		 Annotated Term Reference
Myo3btm1b(EUCOMM)Hmgu/Myo3btm1b(EUCOMM)Hmgu
C57BL/6N-Myo3btm1b(EUCOMM)Hmgu/J 		abnormal bone structure J:211773
convulsive seizures J:211773
decreased leukocyte cell number J:211773
increased bone mineral content J:211773
increased heart weight J:211773
Myo3btm1Pgg/Myo3btm1Pgg
B6.129-Myo3btm1Pgg 		abnormal vestibular hair cell stereociliary bundle morphology J:236347
normal hearing/vestibular/ear phenotype J:236347
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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Send questions and comments to User Support. 		last database update
05/07/2024
MGI 6.23 		The Jackson Laboratory