analgesia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An agnosia that is a loss of the ability to perceive and process pain. (Human Disease Ontology, DOID_0060145)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004270
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Genes

26 gene mutations causing the analgesia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
CDH23 cadherin-related 23
CDK5 cyclin-dependent kinase 5
DLG2 discs, large homolog 2 (Drosophila)
ERBB3 erb-b2 receptor tyrosine kinase 3
KIF1A kinesin family member 1A
KIF1B kinesin family member 1B
KLF7 Kruppel-like factor 7 (ubiquitous)
MAP1B microtubule-associated protein 1B
MAPK6 mitogen-activated protein kinase 6
MC1R melanocortin 1 receptor (alpha melanocyte stimulating hormone receptor)
MUSK muscle, skeletal, receptor tyrosine kinase
MYO6 myosin VI
MYOG myogenin (myogenic factor 4)
NBEA neurobeachin
NRG1 neuregulin 1
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
PCSK2 proprotein convertase subtilisin/kexin type 2
PLCB3 phospholipase C, beta 3 (phosphatidylinositol-specific)
RYR1 ryanodine receptor 1 (skeletal)
SLC17A7 solute carrier family 17 (vesicular glutamate transporter), member 7
SLC7A7 solute carrier family 7 (amino acid transporter light chain, y+L system), member 7
SNAP25 synaptosomal-associated protein, 25kDa
SOX10 SRY (sex determining region Y)-box 10
TMC1 transmembrane channel-like 1
WFS1 Wolfram syndrome 1 (wolframin)