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Phenotypes Associated with This Genotype
Genotype
MGI:5551750
Allelic
Composition
Gt(ROSA)26Sortm1(Tbx1/GFP)Bem/Gt(ROSA)26Sor+
Foxg1tm1(cre)Skm/Foxg1+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Foxg1tm1(cre)Skm mutation (2 available); any Foxg1 mutation (30 available)
Gt(ROSA)26Sortm1(Tbx1/GFP)Bem mutation (1 available); any Gt(ROSA)26Sor mutation (1095 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Thymic aplasia, nasal malformations, and eye, pharyngeal and ear defects in Gt(ROSA)26Sortm1(Tbx1/GFP)Bem/Gt(ROSA)26Sor+ Foxg1tm1(cre)Skm/Foxg1+ mice and microcephaly, ocular and ear defects in Gt(ROSA)26Sortm1(Tbx1/GFP)Bem/Gt(ROSA)26Sor+ Tg(Pax2-cre)1Akg/0 mice

mortality/aging

hearing/vestibular/ear
• hypoplastic to varying degrees, but enlarged in two instances
• enlarged at E14.5

nervous system
• abnormal size and misguided projections
• abnormal size and misguided projections
• abnormal size and misguided projections
• abnormal size and misguided projections

respiratory system

vision/eye

hematopoietic system
• thymic aplasia

craniofacial

taste/olfaction

immune system
• thymic aplasia

endocrine/exocrine glands
• thymic aplasia


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
03/18/2025
MGI 6.24
The Jackson Laboratory