impaired pain sensation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Reduced ability to perceive painful stimuli. (Human Phenotype Ontology, HP_0007328)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007328
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Genes

25 genes associated with the impaired pain sensation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
CCT5 chaperonin containing TCP1, subunit 5 (epsilon)
FBN1 fibrillin 1
FLII flightless I homolog (Drosophila)
GJB1 gap junction protein, beta 1, 32kDa
H19 H19, imprinted maternally expressed transcript (non-protein coding)
HDAC4 histone deacetylase 4
IGF2 insulin-like growth factor 2
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
KCNQ1OT1 KCNQ1 opposite strand/antisense transcript 1 (non-protein coding)
LIFR leukemia inhibitory factor receptor alpha
MFN2 mitofusin 2
MPV17 MpV17 mitochondrial inner membrane protein
NDN necdin, melanoma antigen (MAGE) family member
NGF nerve growth factor (beta polypeptide)
NTRK1 neurotrophic tyrosine kinase, receptor, type 1
OPA1 optic atrophy 1 (autosomal dominant)
PRPS1 phosphoribosyl pyrophosphate synthetase 1
RAI1 retinoic acid induced 1
SCN11A sodium channel, voltage gated, type XI alpha subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
SHANK3 SH3 and multiple ankyrin repeat domains 3
SNRPN small nuclear ribonucleoprotein polypeptide N
WFS1 Wolfram syndrome 1 (wolframin)