Myo1h Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myo1h
myosin 1H
MGI:1914674

5 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Myo1h^{tm1b(KOMP)Wtsi}/Myo1h⁺ C57BL/6N-Myo1h^{tm1b(KOMP)Wtsi}/J	abnormal motor coordination/balance	J:211773
	decreased urine magnesium level	J:211773
Myo1h^{tm1b(KOMP)Wtsi}/Myo1h^{tm1b(KOMP)Wtsi} C57BL/6N-Myo1h^{tm1b(KOMP)Wtsi}/J	abnormal embryo size	J:211773
	embryonic growth retardation	J:211773
	preweaning lethality, complete 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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