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Phenotype Image Detail
Image
Caption External phenotype and skeletal and somite defects in Pofut1cax/Pofut1cax mice. (A-C) Examples of homozygous mutants demonstrating the variable phenotype in the backcross progeny. (D-G) Skeletal preparations of E15.5 embryos showing that even externally apparently normal mice have skeletal defects (D), and demonstrating various defects such as split vertebrae (asterisks in D, F, G), rib fusions and bifurcations (arrowheads in F), reduced or missing pedicles (arrows in G), and axial truncations (E). White and black boxes in (E) indicate the regions shown enlarged in (F) and (G), respectively. (H, I) Sections of E9.5 mutant embryos showing distinct somite borders (indicated by arrowheads) and somites of variable size.
Copyright This image is from Schuster-Gossler K, BMC Dev Biol 2009;9():6, an open-access article, licensee BioMed Central Ltd. J:145608
Associated
Alleles
Symbol Name
Pofut1cax protein O-fucosyltransferase 1; compact axial skeleton
Associated
Genotypes
Allelic Composition Genetic Background
Pofut1cax/Pofut1cax C3H/HeJ-Pofut1cax/J
Pofut1cax/Pofut1cax involves: C57BL/6J * CAST/Ei

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
12/10/2024
MGI 6.24
The Jackson Laboratory