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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Rpl10aem2Mbar
endonuclease-mediated mutation 2, Maria Barna
MGI:7385086
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Rpl10aem2Mbar/Rpl10aem2Mbar C57BL/6-Rpl10aem2Mbar MGI:7385101
cx2
Rpl10aem2Mbar/Rpl10a+
Vangl2Lp/Vangl2+
involves: A * C57BL/6 MGI:7385102


Genotype
MGI:7385101
hm1
Allelic
Composition
Rpl10aem2Mbar/Rpl10aem2Mbar
Genetic
Background
C57BL/6-Rpl10aem2Mbar
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rpl10aem2Mbar mutation (0 available); any Rpl10a mutation (50 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice die after birth
• however, mice are present in normal Mendelian ratios at E18.5

skeleton
• mildly decreased ossification in the radius
• fragments of cartilage unattached to either the spine or sternum instead of a closed rib cage
• at E14.5 with lack of well-defined posterior vertebral elements
• fragments of cartilage unattached to either the spine or sternum instead of a closed rib cage
• little separation of vertebral segments and almost no ossification, particularly at the posterior end

embryo
• absent tissue posterior to the hindlimbs
• beginning at E9.5
• irregularly spaced somites with indistinct boundaries, particularly at the posterior end of the embryo

respiratory system
• less polarized basal feet orientation

nervous system

homeostasis/metabolism

limbs/digits/tail
• complete penetrant loss of the posterior digit in all four limbs
• mildly decreased ossification in the radius

cellular
• less polarized basal feet orientation

cardiovascular system
• ectopic blood vessels




Genotype
MGI:7385102
cx2
Allelic
Composition
Rpl10aem2Mbar/Rpl10a+
Vangl2Lp/Vangl2+
Genetic
Background
involves: A * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Rpl10aem2Mbar mutation (0 available); any Rpl10a mutation (50 available)
Vangl2Lp mutation (2 available); any Vangl2 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• low frequency as in Vangl2Lp heterozygotes

nervous system
• low frequency as in Vangl2Lp heterozygotes





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