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Phenotypes Associated with This Genotype
Genotype
MGI:5304474
Allelic
Composition
Tg(RP11-209M4)#Gglo/Tg(RP11-209M4)#Gglo
Genetic
Background
FVB-Tg(RP11-209M4)#Gglo
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• mice exhibit a wide range of fused and missing digits
• to a greater extent than in mice hemizygous for transgene insertion
• mice exhibit impaired bone formation rate compared with non-transgenic mice and to a greater extent than in mice hemizygous for transgene insertion

limbs/digits/tail
• mice exhibit a wide range of fused and missing digits
• mice exhibit a wide range of fused and missing digits

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
SOST-related sclerosing bone dysplasia DOID:0080036 OMIM:239100
J:99965


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
07/31/2018
MGI 6.12
The Jackson Laboratory