synostosis Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A dysostosis that results_in abnormal fusing of adjacent bones. (Human Disease Ontology, DOID_11971)
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Genes

20 genes involed in the disease synostosis from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ALX4 ALX homeobox 4
ASXL1 additional sex combs like transcriptional regulator 1
CD96 CD96 molecule
CYP26B1 cytochrome P450, family 26, subfamily B, polypeptide 1
ERF Ets2 repressor factor
FGFR1 fibroblast growth factor receptor 1
FGFR2 fibroblast growth factor receptor 2
FGFR3 fibroblast growth factor receptor 3
FREM1 FRAS1 related extracellular matrix 1
GLI3 GLI family zinc finger 3
IL11RA interleukin 11 receptor, alpha
MEGF8 multiple EGF-like-domains 8
MSX2 msh homeobox 2
POR P450 (cytochrome) oxidoreductase
RAB23 RAB23, member RAS oncogene family
RECQL4 RecQ protein-like 4
SKI SKI proto-oncogene
TCF12 transcription factor 12
TGFBR1 transforming growth factor, beta receptor 1
TWIST1 twist family bHLH transcription factor 1