abnormal vertebral body development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomalous formation of the main portion of the vertebra anterior to the vertebral canal, and distinct from the vertebral arch (Mammalian Phenotype Ontology, MP_0005227)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005227
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Genes

7 gene mutations causing the abnormal vertebral body development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMPER BMP binding endothelial regulator
CLEC3B C-type lectin domain family 3, member B
HES7 hes family bHLH transcription factor 7
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NKX3-2 NK3 homeobox 2
TBX6 T-box 6
Funding