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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Sp7tm1Rnis
targeted mutation 1, Riko Nishimura
MGI:5466595
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Sp7tm1Rnis/Sp7tm1Rnis
Tg(Col11a2-cre)1Ntsu/0
involves: C57BL * C57BL/6 * CBA/JNCrlj * DBA/2 MGI:5466671
cn2
Sp7tm1Rnis/Sp7tm1Rnis
Tg(Col2a1-cre)1Bhr/0
involves: C57BL * C57BL/6 * CBA/JNCrlj * SJL MGI:5466672
cn3
Sp7tm1Rnis/Sp7tm1Rnis
Tg(Prrx1-cre)1Cjt/0
involves: C57BL * C57BL/6 * CBA/JNCrlj * SJL/J MGI:5466673


Genotype
MGI:5466671
cn1
Allelic
Composition
Sp7tm1Rnis/Sp7tm1Rnis
Tg(Col11a2-cre)1Ntsu/0
Genetic
Background
involves: C57BL * C57BL/6 * CBA/JNCrlj * DBA/2
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sp7tm1Rnis mutation (1 available); any Sp7 mutation (21 available)
Tg(Col11a2-cre)1Ntsu mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Impairment of ossification in various conditional Sp7tm1Rnis/Sp7tm1Rnis mice

skeleton
• endochondral ossification stopped at the hypertrophic stage




Genotype
MGI:5466672
cn2
Allelic
Composition
Sp7tm1Rnis/Sp7tm1Rnis
Tg(Col2a1-cre)1Bhr/0
Genetic
Background
involves: C57BL * C57BL/6 * CBA/JNCrlj * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sp7tm1Rnis mutation (1 available); any Sp7 mutation (21 available)
Tg(Col2a1-cre)1Bhr mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Impairment of ossification in various conditional Sp7tm1Rnis/Sp7tm1Rnis mice

skeleton
• mice exhibit reduced vascular invasion into cartilage because of insufficient space in non-degraded cartilage tissues indicating disruption in cartilage matric degradation compared to in control mice
• however, mice exhibit normal angiogenesis in the bone collar and apoptosis in hypertrophic chondrocytes
• calcification is inhibited at E17.5 and E18.5
• endochondral ossification stopped at the hypertrophic stage




Genotype
MGI:5466673
cn3
Allelic
Composition
Sp7tm1Rnis/Sp7tm1Rnis
Tg(Prrx1-cre)1Cjt/0
Genetic
Background
involves: C57BL * C57BL/6 * CBA/JNCrlj * SJL/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Sp7tm1Rnis mutation (1 available); any Sp7 mutation (21 available)
Tg(Prrx1-cre)1Cjt mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Impairment of ossification in various conditional Sp7tm1Rnis/Sp7tm1Rnis mice

skeleton
• endochondral ossification stopped at the hypertrophic stage





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory