abnormal intervertebral disk development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the formation of the cartilaginous and gelatinous structure found between vertebrae (Mammalian Phenotype Ontology, MP_0005229)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005229
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9 gene mutations causing the abnormal intervertebral disk development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLEC3B C-type lectin domain family 3, member B
HES7 hes family bHLH transcription factor 7
HSPG2 heparan sulfate proteoglycan 2
KIAA1217 KIAA1217
NELL1 NEL-like 1 (chicken)
NPR3 natriuretic peptide receptor 3
PAX1 paired box 1
TBX6 T-box 6
TWSG1 twisted gastrulation BMP signaling modulator 1