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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rtcatm1a(EUCOMM)Hmgu
targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH
MGI:4841792
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rtcatm1a(EUCOMM)Hmgu/Rtcatm1a(EUCOMM)Hmgu involves: C57BL/6N MGI:5806942


Genotype
MGI:5806942
hm1
Allelic
Composition
Rtcatm1a(EUCOMM)Hmgu/Rtcatm1a(EUCOMM)Hmgu
Genetic
Background
involves: C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rtcatm1a(EUCOMM)Hmgu mutation (0 available); any Rtca mutation (20 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• homozygotes are born at less than the expected Mendelian ratio

nervous system
N
• at 3 weeks after optic nerve crush, adult homozygotes show no differences in retinal ganglion cell (RGC) number and RGC axon morphology in contralateral uninjured retinas or in RGC survival in injured retinas relative to heterozygous or wild-type controls
• at 2 weeks after optic nerve crush, homozygotes operated at P35 show significantly more regenerating RGC axons up to 800 um distal to the lesion site, with some regenerating axons extending over 1.5 mm beyond the crush site, whereas heterozygous and wild-type controls show no obvious axon regrowth beyond the crush site
• at 3 weeks after optic nerve crush, homozygotes operated at 2-3 months of age show a milder phenotype with regenerating RGC axons up to 300 um distal to the lesion site; curving, turning and looping of axons indicates new axon growth, while the furthest distance traveled beyond the injury site is ~3.5 longer than in controls, and a large number of axons are found hundreds of microns beyond the ED1+ crush region unlike in controls





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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
05/14/2024
MGI 6.23
The Jackson Laboratory