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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 11/19/2024 MGI 6.24