About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Utrn
utrophin
MGI:104631
37 phenotypes from multigenic genotypes
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Dmdmdx-3Cv/Dmdmdx-3Cv
Utrntm1Ked/Utrntm1Ked
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
Dmdmdx-3Cv/Y
Utrntm1Ked/Utrntm1Ked
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
Dmdmdx-5Cv/Dmdmdx-5Cv
Flt1tm1Jrt/Flt1+
Utrntm1Jrs/Utrntm1Jrs
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
Dmdmdx/Dmdmdx
Utrntm1Jrs/Utrntm1Jrs
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
Dmdmdx/Dmdmdx
Utrntm1Ked/Utrntm1Ked
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
Dmdmdx/Y
Dtnatm1Jrs/Dtnatm1Jrs
Utrntm1Jrs/Utrntm1Jrs
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
Dmdmdx/Y
Utrntm1Jrs/Utrn+
involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn
diaphragmitis J:140282
myositis J:140282
skeletal muscle endomysial fibrosis J:140282
Dtnatm1Jrs/Dtnatm1Jrs
Utrntm1Jrs/Utrntm1Jrs
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/07/2024
MGI 6.23
The Jackson Laboratory