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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fhl1tm1.1Mihi
targeted mutation 1.1, Michio Hirano
MGI:5705759
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
ot1
Fhl1tm1.1Mihi/Y involves: 129S/SvEv * C57BL/6J * C57BL/6NJ MGI:5706792


Genotype
MGI:5706792
ot1
Allelic
Composition
Fhl1tm1.1Mihi/Y
Genetic
Background
involves: 129S/SvEv * C57BL/6J * C57BL/6NJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fhl1tm1.1Mihi mutation (1 available); any Fhl1 mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• 30% decrease in forelimb grip strength in 7-10 month old males
• however, forelimb and hindlimb muscle strength is not impaired
• decreased latency to fall (30%) as assessed by rotarod is observed in 7-10 month old males
• latency to fall is increased to 35% in 8-10 month old animals

growth/size/body
• by 7-10 months of age body weight is reduced compared to wild-type mice
• proportions of lean tissue, fat and fluid are similar to wild-type

homeostasis/metabolism
• decreased latency to fall (30%) as assessed by rotarod is observed in 7-10 month old males
• latency to fall is increased to 35% in 8-10 month old animals

muscle
• mild myopathy characterized by focal reductions of muscle fiber diameter and increased internal nuclei is observed in 3 out of 7 10 month old males

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
scapuloperoneal myopathy DOID:0060253 OMIM:300695
J:218097





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory