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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Neb
nebulin
MGI:97292
39 phenotypes from 7 alleles in 7 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Nebm1Anu/Nebm2Anu
C57BL/6J-Nebm1Anu Nebm2Anu
abnormal muscle fiber morphology J:285564
abnormal muscle physiology J:285564
abnormal skeletal muscle fiber type ratio J:285564
decreased body size J:285564
decreased grip strength J:285564
decreased locomotor activity J:285564
decreased skeletal muscle fiber diameter J:285564
decreased skeletal muscle fiber size J:285564
impaired skeletal muscle contractility J:285564
increased variability of skeletal muscle fiber size J:285564
Nebm2Anu/Neb+
C57BL/6J-Nebm2Anu
decreased body weight J:285564
Nebm2Anu/Nebm2Anu
C57BL/6J-Nebm2Anu
preweaning lethality, complete penetrance J:285564
Nebtm1(cre)Chen/Nebtm1(cre)Chen
involves: 129S1/Sv * 129X1/SvJ * Black Swiss
abnormal A band morphology J:111470
abnormal I band morphology J:111470
abnormal muscle fiber morphology J:111470
abnormal sarcomere morphology J:111470
abnormal suckling behavior J:111470
abnormal Z line morphology J:111470
decreased body weight J:111470
decreased total body fat amount J:111470
normal muscle phenotype J:111470
postnatal lethality, complete penetrance J:111470
Nebtm1.1Hgra/Nebtm1.1Hgra
involves: C57BL/6 * C57BL/6J * SJL
abnormal muscle physiology J:206854
abnormal sarcomere morphology J:206854
abnormal skeletal muscle fiber morphology J:206854
abnormal Z line morphology J:206854
decreased skeletal muscle fiber size J:206854
muscle weakness J:206854
postnatal growth retardation J:206854
postnatal lethality, complete penetrance J:206854
Nebtm1Slbt/Nebtm1Slbt
involves: 129P2/OlaHsd
abnormal gait J:119578
abnormal H zone morphology J:119578
abnormal muscle contractility J:119578
abnormal sarcomere morphology J:119578
blepharoptosis J:119578
kyphosis J:119578
lethality at weaning, complete penetrance J:119578
postnatal growth retardation J:119578
postnatal lethality, incomplete penetrance J:119578
progressive muscle weakness J:119578
Nebtm2.1Chen/Nebtm2.1Chen
involves: 129 * Black Swiss
abnormal muscle electrophysiology J:211217
increased susceptibility to injury J:211217
normal muscle phenotype J:211217
Nebtm2Hgra/Nebtm2Hgra
Tg(Ckmm-cre)5Khn/0
involves: 129S6/SvEvTac * FVB
abnormal A band morphology J:225840
abnormal H zone morphology J:225840
abnormal muscle fiber morphology J:225840
abnormal sarcomere morphology J:225840
abnormal skeletal muscle fiber size J:225840
abnormal skeletal muscle fiber type ratio J:225840
abnormal Z line morphology J:225840
decreased body weight J:225840
decreased quadriceps weight J:225840
decreased skeletal muscle weight J:225840
impaired exercise endurance J:225840
impaired skeletal muscle contractility J:225840
increased skeletal muscle fiber number J:225840
premature death J:225840

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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last database update
07/02/2024
MGI 6.13
The Jackson Laboratory