sacral vertebral fusion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the union of one or more sacral vertebrae into a single structure in species where this does not normally occur (Mammalian Phenotype Ontology, MP_0004622)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004622
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Genes

12 gene mutations causing the sacral vertebral fusion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARNTL aryl hydrocarbon receptor nuclear translocator-like
AXIN1 axin 1
CHUK conserved helix-loop-helix ubiquitous kinase
GLI3 GLI family zinc finger 3
HOXD10 homeobox D10
HOXD13 homeobox D13
HOXD9 homeobox D9
NACC1 nucleus accumbens associated 1, BEN and BTB (POZ) domain containing
NRARP NOTCH-regulated ankyrin repeat protein
PSEN1 presenilin 1
ROR2 receptor tyrosine kinase-like orphan receptor 2
SULF2 sulfatase 2