abnormal intervertebral disk morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the cartilaginous and gelatinous structure found between vertebrae (Mammalian Phenotype Ontology, MP_0004173)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004173
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Genes

31 gene mutations causing the abnormal intervertebral disk morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACAN aggrecan
ANKH ANKH inorganic pyrophosphate transport regulator
ARNTL aryl hydrocarbon receptor nuclear translocator-like
CLEC3B C-type lectin domain family 3, member B
COL2A1 collagen, type II, alpha 1
ENPP1 ectonucleotide pyrophosphatase/phosphodiesterase 1
FLNB filamin B, beta
GLG1 golgi glycoprotein 1
GLI2 GLI family zinc finger 2
GLRB glycine receptor, beta
HES7 hes family bHLH transcription factor 7
HSPG2 heparan sulfate proteoglycan 2
KIAA1217 KIAA1217
KY kyphoscoliosis peptidase
LASP1 LIM and SH3 protein 1
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
NCDN neurochondrin
NELL1 NEL-like 1 (chicken)
NFIX nuclear factor I/X (CCAAT-binding transcription factor)
NKX3-2 NK3 homeobox 2
NPR3 natriuretic peptide receptor 3
PAX1 paired box 1
QRFPR pyroglutamylated RFamide peptide receptor
ROR2 receptor tyrosine kinase-like orphan receptor 2
T T, brachyury homolog (mouse)
TBX18 T-box 18
TBX6 T-box 6
TP63 tumor protein p63
TRAF4 TNF receptor-associated factor 4
TWSG1 twisted gastrulation BMP signaling modulator 1
ZEB1 zinc finger E-box binding homeobox 1