fusion of vertebral bodies Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect leading to the union of two adjacent vertebrae. (Human Phenotype Ontology, HP_0002948)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004612
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8 gene mutations causing the fusion of vertebral bodies phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP7 bone morphogenetic protein 7
HES7 hes family bHLH transcription factor 7
NOTO notochord homeobox
NRARP NOTCH-regulated ankyrin repeat protein
PLXND1 plexin D1
TBX1 T-box 1
TBX6 T-box 6
UNCX UNC homeobox