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Phenotypes Associated with This Genotype
Genotype
MGI:3618353
Allelic
Composition
Supt20drey/Supt20drey
Genetic
Background
either: C3.B6-Supt20drey or (involves: C3H/HeJ * C57BL/6J)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Supt20drey mutation (0 available); any Supt20 mutation (41 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• only 4% survive postnatally

pigmentation
• 79% exhibit expansion of the retinal-pigmented epithelium over the dorsal half of the eye

vision/eye
• 79% exhibit expansion of the retinal-pigmented epithelium over the dorsal half of the eye

nervous system
• in most homozygous mutant embryos the neural tube fails to close completely
• 14% exhibit neural tube closure defects consisting of spina bifida
• 55% exhibit neural tube closure defects consisting of exencephaly

embryo
• fail to turn; incomplete penetrance
• a small proportion of homozygous embryos exhibit defects of gastrulation
• 3% show severe defects in mesoderm development including a malformed allantois, somite defects, and posterior mesoderm defects
• a small proportion of embryos exhibit posterior truncation
• in most homozygous mutant embryos the neural tube fails to close completely
• 14% exhibit neural tube closure defects consisting of spina bifida
• a small proportion of homozygous embryos exhibit somite defects
• in a small proportion of mutant embryos the allantois is malformed

growth/size/body


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)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory