fused dorsal root ganglion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description loss of DRG spacing pattern and the appearance of two or more ganglia as one (Mammalian Phenotype Ontology, MP_0000963)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000963
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10 gene mutations causing the fused dorsal root ganglion phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CITED2 Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 2
DLL1 delta-like 1 (Drosophila)
DLL3 delta-like 3 (Drosophila)
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
LRP6 low density lipoprotein receptor-related protein 6
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
NRARP NOTCH-regulated ankyrin repeat protein
PSEN1 presenilin 1
TBX18 T-box 18
UNCX UNC homeobox