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Phenotypes Associated with This Genotype
Genotype
MGI:3607793
Allelic
Composition
sau/Del(13)36H
Foxq1sa/Foxq1+
Genetic
Background
involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Del(13)36H mutation (0 available); any Del(13)36H mutation (0 available)
Foxq1sa mutation (16 available); any Foxq1 mutation (30 available)
sau mutation (2 available); any sau mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• hemizygous progeny are born at less than one-third the expected Mendelian frequency, most dying by 16.5 days post coitum (16.5 dpc)

nervous system
• hemizygous embyros examined at 9.5 dpc often exhibit midline forebrain defects and other aspects of holoprocencephaly
• some hemizygotes that survive to birth exhibit holoprosencephalic phenotypes of varying severity

vision/eye
• some hemizygous embryos and liveborn pups exhibit structural eye defects


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
12/30/2025
MGI 6.24
The Jackson Laboratory