split notochord Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the appearance of an abnormal division in the axial fibrocellular cord in embryos around which develops the vertebral primordia (Mammalian Phenotype Ontology, MP_0004713)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004713
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7 gene mutations causing the split notochord phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APC adenomatous polyposis coli
AXIN1 axin 1
EPHA2 EPH receptor A2
GDF3 growth differentiation factor 3
LDB1 LIM domain binding 1
T T, brachyury homolog (mouse)
ZIC3 Zic family member 3