lumbar vertebral fusion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description the union of one or more lumbar vertebrae into a single structure (Mammalian Phenotype Ontology, MP_0004621)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004621
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Genes

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

Symbol Name
AXIN1 axin 1
DMRT2 doublesex and mab-3 related transcription factor 2
GNAI3 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 3
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
NDC1 NDC1 transmembrane nucleoporin
NRARP NOTCH-regulated ankyrin repeat protein
PSEN1 presenilin 1
SMARCAD1 SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
TACC3 transforming, acidic coiled-coil containing protein 3