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Phenotypes Associated with This Genotype
Genotype
MGI:5050501
Allelic
Composition
Whl/Whl
Genetic
Background
involves: BALB/cRl * C3Hf/Rl * C57BL/10Rl
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No mouse lines available in IMSR.
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phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• embryos die E10.5 to E11.5 exhibiting significant growth retardation growth retardation
• normal branching of the vascular network established in the yolk sac and embryo does not occur, compromising blood circulation to the developing embryo

nervous system
• blistering and edema are evident in E10.5-E11.5 embryos
• embryos show a paucity of blood vessels in the most anterior and rostral areas of the forebrain
• anomalies in the organization of the rhombomeric segment boundaries and abnormal flexure of the rhombomeric folds are seen
• alterations in the organization of the rhombomeric segment boundaries and abnormal flexure of the rhombomeric folds are typical

embryo
• alterations in the organization of the rhombomeric segment boundaries and abnormal flexure of the rhombomeric folds are typical

cardiovascular system
• evident at E9.5
• normal branching of the vascular network established in the yolk sac and embryo does not occur compromising blood circulation to the developing embryo
• there are fewer than normal blood vessels in the most anterior and rostral regions of the forebrain regions of the forebrain regions of the forebrain
• abnormal sprouting of vessels in the intersomitic region indicates defects in vascular patterning

hearing/vestibular/ear
• during development the primordia of the lateral and posterior canal are reduced in size and the fusion process delayed


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
06/12/2024
MGI 6.13
The Jackson Laboratory