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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Myo10tm1a(KOMP)Wtsi
targeted mutation 1a, Wellcome Trust Sanger Institute
MGI:4362586
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Myo10tm1a(KOMP)Wtsi/Myo10tm1a(KOMP)Wtsi involves: C57BL/6N MGI:6116651


Genotype
MGI:6116651
hm1
Allelic
Composition
Myo10tm1a(KOMP)Wtsi/Myo10tm1a(KOMP)Wtsi
Genetic
Background
involves: C57BL/6N
Cell Lines EPD0332_3_B02
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myo10tm1a(KOMP)Wtsi mutation (2 available); any Myo10 mutation (612 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only 45% of homozygotes survived birth and grew to adulthood
• homozygous mutant pups from heterozygous matings were obtained at less than half (45%) the expected number, suggesting a high frequency of embryonic or perinatal lethality

nervous system
• at E12.5, 9 of 18 (50%) embryos resulting from 2 homozygous crosses exhibited exencephaly

vision/eye
• all adult homozygotes whose eyes were dissected (5 of 5) had persistent hyaloid vasculature that was pigmented and bilateral

pigmentation
• all surviving homozygotes had a white belly spot; a few also had a white spot on the back
• all surviving homozygotes had a white belly spot

limbs/digits/tail
• ~50% of adult homozygotes had webbed digits, usually on the forelimbs
• ~50% of adult homozygotes had a kink near the tip of the tail

integument
• all surviving homozygotes had a white belly spot; a few also had a white spot on the back
• all surviving homozygotes had a white belly spot





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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
11/12/2024
MGI 6.24
The Jackson Laboratory