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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Otx1tm3(OTX2)Asim
targeted mutation 3, Antonio Simeone
MGI:2153200
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Otx1tm3(OTX2)Asim/Otx1tm3(OTX2)Asim involves: 129P2/OlaHsd * C57BL/6 * DBA/2 MGI:3845659


Genotype
MGI:3845659
hm1
Allelic
Composition
Otx1tm3(OTX2)Asim/Otx1tm3(OTX2)Asim
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Otx1tm3(OTX2)Asim mutation (0 available); any Otx1 mutation (86 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• the postnatal lethality observed in Otx1tm1Asim homozygotes is rescued

nervous system
N
• compared to Otx1tm1Asim homozygotes, the telencephalic cortex is thickened and the regions located dorsally and ventrally to the presumptive sulcus rhinalis are restored to normal size
• cell proliferation in the dorsal telencephalon is greater than in Otx1tm1Asim homozygotes
• in 50% of mice
• mice exhibit reduced brain size compared with wild-type mice that is not as severe as in Otx1tm1Asim homozygotes
• mice exhibit reduced brain mass compared with wild-type mice that is not as severe as in Otx1tm1Asim homozygotes
• 45% of mice exhibit a reduction in mesencephalon size compared to in wild-type mice

hearing/vestibular/ear
• mice exhibit a partial rescue of inner ear defects observed in Otx1tm1Asim homozygotes

vision/eye
• in 25% of mice
• 30% of mice lack the ciliary process

behavior/neurological
N
• unlike Otx1tm1Asim homozygotes, mice exhibit moderate-speed turning behavior and lack seizures

endocrine/exocrine glands
• in 25% of mice
• in 25% of mice





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last database update
10/29/2024
MGI 6.24
The Jackson Laboratory