persistence of notochord tissue Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description failure of notochord tissue to differentiate into the vertebral primordia during development resulting in the presence of notochord tissue at later stages than it is normally seen (Mammalian Phenotype Ontology, MP_0004711)
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4 gene mutations causing the persistence of notochord tissue phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
COL2A1 collagen, type II, alpha 1
GLI2 GLI family zinc finger 2
NKX3-2 NK3 homeobox 2
TWSG1 twisted gastrulation BMP signaling modulator 1