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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Txnrd1tm1.1Marc
targeted mutation 1.1, Marcus Conrad
MGI:3574773
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Txnrd1tm1.1Marc/Txnrd1tm1.1Marc involves: 129P2/OlaHsd * C57BL/6J MGI:3574775
cn2
Myl2tm1(cre)Krc/Myl2+
Txnrd1tm1Marc/Txnrd1tm1.1Marc
involves: 129P2/OlaHsd * C57BL/6J MGI:3574776


Genotype
MGI:3574775
hm1
Allelic
Composition
Txnrd1tm1.1Marc/Txnrd1tm1.1Marc
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Txnrd1tm1.1Marc mutation (0 available); any Txnrd1 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• frequently observed embryo resorption between E9.5 and E10.5

cellular
• the number of proliferating cells in E9.5 and E10.5 null embryos was reduced
• establishment of proliferating MEFs from homozygous null embryos failed as cells were not capable of proliferating

embryo
• at E10.5, embryos failed to turn
• the anterior-posterior axis of E10.5 embryos was markedly shortened
• development of embryos was retarded with the E10.5 embryo head region resembling that of the E9 wildtype embryo and tissues caudal to the heart resembling the morphology of E8.5 or earlier wildtype embryos
• reduced size of the deciduas and embryos between E8.5 and E10.5, however the layering and size of trophoblast giant cells at the proximal pole of the deciduas seemed normal
• positioning and size of the E9.5 null embryos resembled those of E7.5 wildtype embryos
• E10.5 embryos had a neural tube closure defect with an overall structure comparable to that of the E8.5 wildtype embryo
• impaired somitogenesis
• primary vascular plexus formation in the yolk sac was delayed but blood vessel formation appeared unaffected

growth/size/body
• reduced size of the deciduas and embryos between E8.5 and E10.5, however the layering and size of trophoblast giant cells at the proximal pole of the deciduas seemed normal
• positioning and size of the E9.5 null embryos resembled those of E7.5 wildtype embryos

nervous system
• E10.5 embryos had a neural tube closure defect with an overall structure comparable to that of the E8.5 wildtype embryo




Genotype
MGI:3574776
cn2
Allelic
Composition
Myl2tm1(cre)Krc/Myl2+
Txnrd1tm1Marc/Txnrd1tm1.1Marc
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myl2tm1(cre)Krc mutation (2 available); any Myl2 mutation (22 available)
Txnrd1tm1.1Marc mutation (0 available); any Txnrd1 mutation (49 available)
Txnrd1tm1Marc mutation (1 available); any Txnrd1 mutation (49 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
N
• no differences in heart shape or in the cellular morphology of cardiomyocytes





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory