Utrn Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Utrn
utrophin
MGI:104631

37 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Dmd^mdx-3Cv/Dmd^mdx-3Cv Utrn^tm1Ked/Utrn^tm1Ked involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	abnormal skeletal muscle morphology	J:116348
	normal liver/biliary system phenotype	J:116348
	normal nervous system phenotype	J:116348
	normal renal/urinary system phenotype	J:116348
	normal reproductive system phenotype	J:116348
	normal respiratory system phenotype	J:116348
Dmd^mdx-3Cv/Y Utrn^tm1Ked/Utrn^tm1Ked involves: 129 * C3H/HeHa * C57BL * M. m. castaneus * M. m. musculus	abnormal skeletal muscle morphology	J:116348
	normal liver/biliary system phenotype	J:116348
	normal nervous system phenotype	J:116348
	normal renal/urinary system phenotype	J:116348
	normal reproductive system phenotype	J:116348
	normal respiratory system phenotype	J:116348
Dmd^mdx-5Cv/Dmd^mdx-5Cv Flt1^tm1Jrt/Flt1⁺ Utrn^tm1Jrs/Utrn^tm1Jrs involves: 129S1/Sv * 129X1/SvJ * C3HA * C57BL/6Ros	centrally nucleated skeletal muscle fibers	J:164891
	extended life span	J:164891
	increased body weight	J:164891
Dmd^mdx/Dmd^mdx Utrn^tm1Jrs/Utrn^tm1Jrs involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	abnormal gait	J:42389
	abnormal limb morphology	J:42389, J:59675
	abnormal muscle physiology	J:42389
	abnormal muscle relaxation	J:42389
	abnormal neuromuscular synapse morphology	J:42389, J:60776
	cardiomyopathy	J:42389, J:59675
	decreased body size	J:42389
	dystrophic muscle	J:42389, J:59675
	kyphosis	J:42389, J:59675
	muscle degeneration	J:42389
	muscle weakness	J:42389
	myocardium necrosis	J:42389
	postnatal growth retardation	J:42389, J:59675
	premature death	J:42389, J:59675
	skeletal muscle interstitial fibrosis	J:42389
	skeletal muscle necrosis	J:42389
Dmd^mdx/Dmd^mdx Utrn^tm1Ked/Utrn^tm1Ked involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA	abnormal breathing pattern	J:42388
	abnormal gait	J:42388
	abnormal hindlimb morphology	J:42388
	abnormal neuromuscular synapse morphology	J:42388
	abnormal posture	J:42388
	abnormal skeletal muscle fiber morphology	J:42388
	abnormal skeletal muscle fiber size	J:42388
	centrally nucleated skeletal muscle fibers	J:42388
	decreased locomotor activity	J:42388
	dystrophic muscle	J:42388
	kyphosis	J:42388
	premature death	J:42388
	progressive muscle weakness	J:42388
	skeletal muscle interstitial fibrosis	J:42388
	skeletal muscle necrosis	J:42388
	weight loss	J:42388
Dmd^mdx/Y Dtna^tm1Jrs/Dtna^tm1Jrs Utrn^tm1Jrs/Utrn^tm1Jrs involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	abnormal limb morphology	J:59675
	abnormal neuromuscular synapse morphology	J:60776
	cardiomyopathy	J:59675
	dystrophic muscle	J:59675
	kyphosis	J:59675
	postnatal growth retardation	J:59675
	postnatal lethality, incomplete penetrance	J:59675
	premature death	J:59675
	skeletal muscle necrosis	J:59675
Dmd^mdx/Y Utrn^tm1Jrs/Utrn⁺ involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn	diaphragmitis	J:140282
	myositis	J:140282
	skeletal muscle endomysial fibrosis	J:140282
Dtna^tm1Jrs/Dtna^tm1Jrs Utrn^tm1Jrs/Utrn^tm1Jrs involves: 129S1/Sv * 129X1/SvJ	abnormal neuromuscular synapse morphology	J:60776
	cardiomyopathy	J:59675
	dystrophic muscle	J:59675

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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