joint swelling Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001386
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Genes

28 genes associated with the joint swelling phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
ANKH ANKH inorganic pyrophosphate transport regulator
ANKRD55 ankyrin repeat domain 55
ASAH1 N-acylsphingosine amidohydrolase (acid ceramidase) 1
CD247 CD247 molecule
FAS Fas cell surface death receptor
FGA fibrinogen alpha chain
FGB fibrinogen beta chain
FGG fibrinogen gamma chain
HGD homogentisate 1,2-dioxygenase
HPGD hydroxyprostaglandin dehydrogenase 15-(NAD)
IL1RN interleukin 1 receptor antagonist
IL2RA interleukin 2 receptor, alpha
IL2RB interleukin 2 receptor, beta
IL6 interleukin 6
LMX1B LIM homeobox transcription factor 1, beta
MED12 mediator complex subunit 12
MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor)
NOD2 nucleotide-binding oligomerization domain containing 2
OCRL oculocerebrorenal syndrome of Lowe
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PTPN2 protein tyrosine phosphatase, non-receptor type 2
PTPN22 protein tyrosine phosphatase, non-receptor type 22 (lymphoid)
SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1
SLCO2A1 solute carrier organic anion transporter family, member 2A1
STAT4 signal transducer and activator of transcription 4
TYK2 tyrosine kinase 2
WISP3 WNT1 inducible signaling pathway protein 3