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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
sau
sauron
MGI:3607721
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Foxq1sa/Foxq1+
sau/sau+
involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR MGI:3607722
cx2
sau/Del(13)36H
Foxq1sa/Foxq1+
involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR MGI:3607793


Genotype
MGI:3607722
cx1
Allelic
Composition
Foxq1sa/Foxq1+
sau/sau+
Genetic
Background
involves: 101 * BALB/cOlaHsd * C3H * C57BL/6J * C57BR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxq1sa mutation (16 available); any Foxq1 mutation (29 available)
sau mutation (2 available); any sau mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• heterozygous mice exhibit heightened anxiety in the Open Field Activity test, entering the center of the field 29% less frequently than littermate controls




Genotype
MGI:3607793
cx2
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 (29 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





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory