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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Recktm2.2Noda
targeted mutation 2.2, Makoto Noda
MGI:5428466
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Recktm1.1Noda/Recktm2.2Noda involves: 129P2/OlaHsd * C57BL/6NCrlj * CBA/JNCrlj MGI:5428662
cn2
Recktm2.1Noda/Recktm2.2Noda
Tg(Prrx1-cre)1Cjt/0
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * FVB/N * SJL/J MGI:5428660
cn3
Recktm2.1Noda/Recktm2.2Noda
Tg(Col2a1-cre)1Bhr/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL MGI:5428659
cn4
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Recktm2.2Noda/Recktm3.1(cre/ERT2)Noda
involves: 129S4/SvJaeSor * C57BL/6 * FVB/N MGI:5428661


Genotype
MGI:5428662
ht1
Allelic
Composition
Recktm1.1Noda/Recktm2.2Noda
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6NCrlj * CBA/JNCrlj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Recktm1.1Noda mutation (0 available); any Reck mutation (46 available)
Recktm2.2Noda mutation (1 available); any Reck mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• with multiple cutaneous horns on the dorsal side of the extremities
• as early as E12.5 in the forelimb buds
• the posterior side is hypoplastic
• poor chondrocyte condensation
• increased cell density in the central area and uneven, spongy distribution of cells in the marginal areas
• hypoplastic without an increase in apoptosis
• the dorsal ectoderm cells exhibit altered appearance
• fingertip bones are round and porous in all limbs
• in some mice one or both of the forelimbs are pointing backwards
• mice exhibit loss of postaxial forelimb structures with variable severity
• more severe in the right forelimb
• in some mice with forelimb pointing backward

embryo
• as early as E12.5 in the forelimb buds
• the posterior side is hypoplastic
• poor chondrocyte condensation
• increased cell density in the central area and uneven, spongy distribution of cells in the marginal areas
• hypoplastic without an increase in apoptosis
• the dorsal ectoderm cells exhibit altered appearance

skeleton
• in some mice with forelimb pointing backward




Genotype
MGI:5428660
cn2
Allelic
Composition
Recktm2.1Noda/Recktm2.2Noda
Tg(Prrx1-cre)1Cjt/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * FVB/N * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Recktm2.1Noda mutation (1 available); any Reck mutation (46 available)
Recktm2.2Noda mutation (1 available); any Reck mutation (46 available)
Tg(Prrx1-cre)1Cjt mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
N
• authors state that mice exhibit the same defects as in Recktm1.1Noda/Recktm2.1Noda mice




Genotype
MGI:5428659
cn3
Allelic
Composition
Recktm2.1Noda/Recktm2.2Noda
Tg(Col2a1-cre)1Bhr/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Recktm2.1Noda mutation (1 available); any Reck mutation (46 available)
Recktm2.2Noda mutation (1 available); any Reck mutation (46 available)
Tg(Col2a1-cre)1Bhr mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
N
• mice exhibit normal limb patterning




Genotype
MGI:5428661
cn4
Allelic
Composition
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
Recktm2.2Noda/Recktm3.1(cre/ERT2)Noda
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1Sor mutation (7 available); any Gt(ROSA)26Sor mutation (993 available)
Recktm2.2Noda mutation (1 available); any Reck mutation (46 available)
Recktm3.1(cre/ERT2)Noda mutation (0 available); any Reck mutation (46 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• mice exhibit abnormal distribution of Reck+ cells compared with control mice





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