About   Help   FAQ
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 (8 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





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