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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Rarb-cre)1Mrc
transgene insertion 1, Mario R Capecchi
MGI:2159107
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Wnt3tm1Amc/Wnt3tm2Amc
Tg(Rarb-cre)1Mrc/0
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ MGI:2450913
cn2
Fgf4tm1Mrc/Fgf4tm1.1Mrc
Tg(Rarb-cre)1Mrc/0
involves: 129S1/Sv * 129X1/SvJ MGI:3713885
cn3
Fgf4tm1Mrc/Fgf4tm2Mrc
Tg(Rarb-cre)1Mrc/0
involves: 129S1/Sv * 129X1/SvJ MGI:2176789
cn4
Fgf8tm1Mrc/Fgf8tm2Mrc
Tg(Rarb-cre)1Mrc/0
Not Specified MGI:2176855
cn5
Aldh1a2tm1Dll/Aldh1a2tm1Ipc
Tg(Rarb-cre)1Mrc/0
Not Specified MGI:3575693


Genotype
MGI:2450913
cn1
Allelic
Composition
Wnt3tm1Amc/Wnt3tm2Amc
Tg(Rarb-cre)1Mrc/0
Genetic
Background
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Rarb-cre)1Mrc mutation (1 available)
Wnt3tm1Amc mutation (0 available); any Wnt3 mutation (25 available)
Wnt3tm2Amc mutation (0 available); any Wnt3 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• at E10.5, mutant mice exhibit a reduction in the anterior/posterior length of the AER
• mutant mice display variable forelimb defects ranging from three digits (anterior digits 1-3) and normal zeugopod (radius and ulna) to one digit (digit 2 or 3) and also zeugopod defects (missing ulna); in most cases, the humerus appears unaffected

embryo
• at E10.5, mutant mice exhibit a reduction in the anterior/posterior length of the AER




Genotype
MGI:3713885
cn2
Allelic
Composition
Fgf4tm1Mrc/Fgf4tm1.1Mrc
Tg(Rarb-cre)1Mrc/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf4tm1.1Mrc mutation (0 available); any Fgf4 mutation (30 available)
Fgf4tm1Mrc mutation (0 available); any Fgf4 mutation (30 available)
Tg(Rarb-cre)1Mrc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
N
• mutants at E15.5, at birth, and as adults have normal forelimbs




Genotype
MGI:2176789
cn3
Allelic
Composition
Fgf4tm1Mrc/Fgf4tm2Mrc
Tg(Rarb-cre)1Mrc/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf4tm1Mrc mutation (0 available); any Fgf4 mutation (30 available)
Fgf4tm2Mrc mutation (0 available); any Fgf4 mutation (30 available)
Tg(Rarb-cre)1Mrc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
N
• no abnormal limbs/digits/tail phenotypes detected

skeleton
N
• no abnormal skeleton phenotypes detected




Genotype
MGI:2176855
cn4
Allelic
Composition
Fgf8tm1Mrc/Fgf8tm2Mrc
Tg(Rarb-cre)1Mrc/0
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf8tm1Mrc mutation (0 available); any Fgf8 mutation (21 available)
Fgf8tm2Mrc mutation (0 available); any Fgf8 mutation (21 available)
Tg(Rarb-cre)1Mrc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype



Genotype
MGI:3575693
cn5
Allelic
Composition
Aldh1a2tm1Dll/Aldh1a2tm1Ipc
Tg(Rarb-cre)1Mrc/0
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Aldh1a2tm1Dll mutation (0 available); any Aldh1a2 mutation (38 available)
Aldh1a2tm1Ipc mutation (0 available); any Aldh1a2 mutation (38 available)
Tg(Rarb-cre)1Mrc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• abnormal flexure of the forepaw digits, especially of second and third digits
• partial syndactyly of the second to forth forelimb digits

muscle
N
• no defect in the size and topology of distal limb muscle groups and their intersections, except for a slight hypoplasia of the extensor radialis muscles

skeleton
N
• no defect in digit skeleton

nervous system
• an early embryonic loss of a subset of Lim1+ brachial motoneurons, a mispositioning of Islet1+ neurons and inappropriate axonal projections of the nerves innervating extensor limb muscles





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory