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Phenotypes Associated with This Genotype
Genotype
MGI:2450742
Allelic
Composition
Pdgfratm8Sor/Pdgfratm8Sor
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
H2az2Tg(Wnt1-cre)11Rth mutation (2 available); any H2az2 mutation (25 available)
Pdgfratm8Sor mutation (1 available); any Pdgfra mutation (88 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• abnormal origin of the right subclavian artery
• observed between E17.7-E18.5
• midline hemorrhage

craniofacial
• phenotype varied in severity; the frontal bones were absent or failed to fuse
• phenotype varied in severity; the nasal bones were absent or failed to fuse
• developmental defects appear at E11.5 with a gap in the frontal nasal processes and progresses to hemorrhaging and blebbing by E13.5
• phenotype varied in severity; the nasal capsule was absent or failed to fuse
• snouts shortened by 8%
• phenotype varied in severity due to defects in the nasal capsule and/or frontal and nasal bones

immune system
• observed with very low penetrance (3 out of 32 homozygous mutant embryos)

skeleton
• phenotype varied in severity; the frontal bones were absent or failed to fuse
• phenotype varied in severity; the nasal bones were absent or failed to fuse
• phenotype varied in severity; the nasal capsule was absent or failed to fuse

hematopoietic system
• observed with very low penetrance (3 out of 32 homozygous mutant embryos)

respiratory system
• phenotype varied in severity; the nasal bones were absent or failed to fuse
• phenotype varied in severity; the nasal capsule was absent or failed to fuse

endocrine/exocrine glands
• observed with very low penetrance (3 out of 32 homozygous mutant embryos)

growth/size/body
• phenotype varied in severity; the frontal bones were absent or failed to fuse
• phenotype varied in severity; the nasal bones were absent or failed to fuse
• phenotype varied in severity; the nasal capsule was absent or failed to fuse
• snouts shortened by 8%
• phenotype varied in severity due to defects in the nasal capsule and/or frontal and nasal bones


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
01/06/2026
MGI 6.24
The Jackson Laboratory