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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Myf6tm1Wb
targeted mutation 1, Barbara Wold
MGI:1857220
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Myf6tm1Wb/Myf6tm1Wb involves: 129S1/Sv * C57BL/6 MGI:2175131
cx2
Myf5tm1Jae/Myf5+
Myf6tm1Wb/Myf6+
involves: 129S1/Sv * 129S4/SvJae MGI:3714407


Genotype
MGI:2175131
hm1
Allelic
Composition
Myf6tm1Wb/Myf6tm1Wb
Genetic
Background
involves: 129S1/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myf6tm1Wb mutation (1 available); any Myf6 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• die shortly after birth

respiratory system
• unable to breathe

skeleton
• rib foreshortening leads to variable failure to join the sternum
• rib development is severely disturbed in newborns
• some ribs display abnormal angles of extension
• fusion of rib cartilage from adjacent ribs
• rib foreshortening in ribs 2-12 is usually less than 20% of total length and leads to variable failure to join the sternum
• the first and last ribs are more dramatically shortened compared to others
• truncated ribs that fail to attach to the sternum
• the tuberculum anterior is absent on the 6th cervical vertebrae of most mice
• disorganized ossification in the sternum

muscle
• although earliest myotome formation is unaffected, mutants exhibit a deficit in myotome development beginning around E9 and ending around E11
• myotomes are greatly reduced in size and cell number at E11
• some intercostals muscles associated with ribs 35 are either disorganized or significantly reduced in fiber number at E18.5 and in newborns




Genotype
MGI:3714407
cx2
Allelic
Composition
Myf5tm1Jae/Myf5+
Myf6tm1Wb/Myf6+
Genetic
Background
involves: 129S1/Sv * 129S4/SvJae
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myf5tm1Jae mutation (1 available); any Myf5 mutation (17 available)
Myf6tm1Wb mutation (1 available); any Myf6 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• double heterozygous mice in which the Myf5 and Myf6 alleles are on different chromosomes show severely reduced expression of Myf5 and die at birth due to respiratory distress

respiratory system

skeleton
• sternum shows irregular ossification of sternebrae
• none of the first seven ribs are attached to the sternum
• fusion of adjacent ribs
• short ribs; ribs are shorter than in wild-type or Myf6 homozygotes but longer than the stubs of Myf5 homozygotes

muscle
• myotomes are disorganized at E10.5





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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
12/10/2024
MGI 6.24
The Jackson Laboratory