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Phenotypes Associated with This Genotype
Genotype
MGI:2451064
Allelic
Composition
Bmp7tm1Rob/Bmp7tm1Rob
Genetic
Background
either: (involves: 129S/SvEv * C57BL/6J) or (involves: 129S/SvEv * MF1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Bmp7tm1Rob mutation (2 available); any Bmp7 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• ~95% die within a day of birth
• the remaining 5% die within 5-10 days of birth

limbs/digits/tail
• ~33% exhbibited hind limb polydactyly, mixed background involving either C57BL/6J or MF1
• 1 mouse (of 14) was observed with hind limb polydactyly on the 129S/SvEv background

renal/urinary system
• bilateral renal dysplasia
• observed in both inbred and mixed backgrounds
• often accompanying renal dysplasia

vision/eye
• ~20% exhibited bilateral microphthalmia
• ~20% exhibited unilateral anophthalmia in combination with unilateral microphthalmia
• proportions observed on both inbred and mixed genetic backgrounds
• ~60% exhibited bilateral anophthalmia
• ~20% exhibited unilateral anophthalmia in combination with unilateral microphthalmia
• proportions observed on both inbred and mixed genetic backgrounds

skeleton
• about 50% of mice display minor axial skeletal abnormalities
• occasionally, membranous bones in cranial region are not fully developed
• prevalent axial skeletal defect is failure of one or both of seventh rib pair to fuse to sternum, usually accompanied by absence of an obvious fourth sternebral ossification center

craniofacial
• occasionally, membranous bones in cranial region are not fully developed

nervous system
• exencephaly is observed in very low percentage of late stage or perinatal mutant mice


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
04/16/2024
MGI 6.23
The Jackson Laboratory