Myh1 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Myh1
myosin, heavy polypeptide 1, skeletal muscle, adult
MGI:1339711

27 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Myh1^{tm1b(KOMP)Wtsi}/Myh1^{tm1b(KOMP)Wtsi} C57BL/6N-Myh1^{tm1b(KOMP)Wtsi}/J	abnormal auditory brainstem response	J:211773
	abnormal bone structure	J:211773
	abnormal sleep behavior	J:211773
	abnormal startle reflex	J:211773
	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	decreased exploration in new environment	J:211773
	decreased grip strength	J:211773
	decreased leukocyte cell number	J:211773
	decreased prepulse inhibition	J:211773
	decreased thigmotaxis	J:211773
	decreased urine creatinine level	J:211773
	decreased urine glucose level	J:211773
	decreased urine magnesium level	J:211773
	increased erythrocyte cell number	J:211773
	increased hematocrit	J:211773
	increased hemoglobin content	J:211773
	increased total body fat amount	J:211773
Myh1^tm1Lnwd/Myh1^tm1Lnwd involves: 129/Ola * 129P2/OlaHsd * C57BL/6	abnormal skeletal muscle fiber type ratio	J:48228
	abnormal skeletal muscle morphology	J:44448, J:78284
	decreased body weight	J:44448
	decreased fluid intake	J:44448
	decreased food intake	J:44448
	decreased grip strength	J:44448
	decreased skeletal muscle mass	J:44448
	impaired skeletal muscle contractility	J:44448
	kyphosis	J:44448
	muscle weakness	J:44448

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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