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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fubp1tm1.1Dlev
targeted mutation 1.1, David Levens
MGI:5789037
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fubp1tm1.1Dlev/Fubp1tm1.1Dlev involves: 129 * C57BL/6 MGI:5792828


Genotype
MGI:5792828
hm1
Allelic
Composition
Fubp1tm1.1Dlev/Fubp1tm1.1Dlev
Genetic
Background
involves: 129 * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fubp1tm1.1Dlev mutation (0 available); any Fubp1 mutation (54 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• a single live-born pup was pale, runt, in obvious respiratory distress, and died within 15 minutes of birth
• all delivered embryos (6%) are stillborn, with a single exception that died within 15 minutes of birth
• homozygous embryos die steadily across a wide developmental span from ~E10.5 until birth

growth/size/body
• concentric hypertrophy of the cardiac ventricular wall at E19.5, suggesting increased vascular resistance
• average gestational age-adjusted weight of live embryos is ~20% below that of wild-type controls
• some of the embryos euthanized at E13.5 to E19.5 appear runted
• embryos appear growth restricted

embryo
• placentas appear thinner and poorly developed at E19.5
• a striking number of microcalcifications are seen along the giant cell and spongiotrophoblastic layers, suggesting placental distress
• poorly formed maternal vascular spaces at E19.5
• collapse of the labyrinth reduces placenta thickness at E19.5

immune system
• a severely hypoplastic spleen is often seen at E19.5
• significant B-cell lymphopenia at E13.5 and E19.5
• a severely hypoplastic spleen is often seen at E19.5
• marked underdevelopment of lymphoid tissues at E19.5

cardiovascular system
• concentric hypertrophy of the cardiac ventricular wall at E19.5, suggesting increased vascular resistance
• the thin-walled capillary bed of fetal circulation is ill defined
• some of the embryos euthanized at E13.5 to E19.5 are hemorrhagic

liver/biliary system
• embryonic livers are often small
• embryonic livers are often pale

hematopoietic system
• a severely hypoplastic spleen is often seen at E19.5
• variable, multi-lineage hematopoietic deficiency at E13.5 and E19.5, with deficits in erythroid, granulocyte/macrophage, and lymphoid lineages, as shown by immunophenotyping of fetal liver cells and colony-forming assays
• significant red cell anemia at E13.5 and E19.5
• bone marrow hypoplasia at E19.5
• significantly decreased number of hepatic megakaryocytes at E19.5
• significant B-cell lymphopenia at E13.5 and E19.5
• rarefaction of hepatic and bone marrow hematopoietic precursors across all lineages at E19.5, suggesting impaired hematopoiesis
• significantly reduced numbers of hematopoietic progenitor cells at E13.5 and E19.5, as shown by colony-forming assays
• a severely hypoplastic spleen is often seen at E19.5
• despite normal or even increased numbers of hematopoietic stem cells (HSCs), transplantation of mutant HSCs into lethally irradiated mice fails to reconstitute hematopoiesis

respiratory system
• markedly small lungs at E19.5
• marked lung hypoplasia at E19.5
• broad, thick-walled terminal sacs lined by primarily bronchial-type cuboidal epithelium at E19.5
• reduced branching of air spaces at E19.5

nervous system
• marked brain parenchymal hypercellularity at E19.5
• cerebral hyperplasia at E19.5
• reduced organization of layers I to VI of the diencephalic cortex with less distinct cortical layering at E19.5
• no cerebellar lobations are present at the level of the choroid plexus in the IV ventricle at E19.5

integument
• some of the embryos euthanized at E13.5 to E19.5 appear pale

endocrine/exocrine glands
• a severely hypoplastic spleen is often seen at E19.5





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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
11/12/2024
MGI 6.24
The Jackson Laboratory