small vertebral body Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decreased size of the main cylindrical portion of the vertebra ventral to the vertebral canal (Mammalian Phenotype Ontology, MP_0004670)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004670
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Genes

15 gene mutations causing the small vertebral body phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMPER BMP binding endothelial regulator
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
CHRD chordin
COL1A1 collagen, type I, alpha 1
COL2A1 collagen, type II, alpha 1
FGFR3 fibroblast growth factor receptor 3
FOXC1 forkhead box C1
FOXC2 forkhead box C2
LASP1 LIM and SH3 protein 1
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NKX3-2 NK3 homeobox 2
PAX1 paired box 1
PTH parathyroid hormone
ROR2 receptor tyrosine kinase-like orphan receptor 2
TBX6 T-box 6