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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Klhl40tm1(KOMP)Vlcg
targeted mutation 1, Velocigene
MGI:4843038
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Klhl40tm1(KOMP)Vlcg/Klhl40tm1(KOMP)Vlcg C57BL/6-Klhl40tm1(KOMP)Vlcg MGI:5774663


Genotype
MGI:5774663
hm1
Allelic
Composition
Klhl40tm1(KOMP)Vlcg/Klhl40tm1(KOMP)Vlcg
Genetic
Background
C57BL/6-Klhl40tm1(KOMP)Vlcg
Cell Lines 14780A-B6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Klhl40tm1(KOMP)Vlcg mutation (0 available); any Klhl40 mutation (26 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Small size of P8 Klhl40tm1(KOMP)Vlcg/Klhl40tm1(KOMP)Vlcg pups

mortality/aging
• 50% of mice die by 7 days of age and none survive past 3 weeks of age

growth/size/body
• at P8, surviving mice are visibly smaller than wild-type controls
• mice exhibit reduced growth within several days of birth

muscle
• at P8, a subset of diaphragm muscle fibers show complete loss of sarcomere organization
• however, sarcomere thin filament lengths are not decreased in P5 tibialis anterior muscles
• at P8, a subset of diaphragm muscle fibers exhibit widened Z-discs that resemble nemaline bodies
• other diaphragm myofibers display irregular, wave-like structures known as Z line streaming
• at P1, diaphragm muscles appear relatively normal; however, subtle Z-line defects may be present
• expression analysis of thin filament proteins revealed that nebulin (NEB) is decreased by ~50% while leiomodin 3 (LMOD3) is nearly abolished in P1 and P8 quadriceps muscles, leading to destabilization of thin filaments and sarcomere dysfunction
• severe skeletal muscle dysfunction that likely contributes to lethality
• at P1, the maximum tetanic force of whole hind limbs following 150-Hz stimulation is reduced by >50%
• >50% reduction in hind limb strength at P1
• mice develop a nemaline-like myopathy

cardiovascular system
• at P5-P11, hearts are smaller but otherwise normal
• at P5, heart rate is decreased by 15%
• however, fractional shortening is relatively normal

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
nemaline myopathy 8 DOID:0110930 OMIM:615348
J:213780





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory