Excessive Tearing Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0152227
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Genes

24 genes associated with the disease Excessive Tearing in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADRB2 adrenoceptor beta 2, surface
ANKRD11 ankyrin repeat domain 11
ARSD arylsulfatase D
COL17A1 collagen, type XVII, alpha 1
DCPS decapping enzyme, scavenger
DKC1 dyskeratosis congenita 1, dyskerin
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
IGSF3 immunoglobulin superfamily, member 3
IRX5 iroquois homeobox 5
KRT12 keratin 12, type I
KRT3 keratin 3, type II
LRP1 low density lipoprotein receptor-related protein 1
MOXD1 monooxygenase, DBH-like 1
NHP2 NHP2 ribonucleoprotein
NLRP3 NLR family, pyrin domain containing 3
NOP10 NOP10 ribonucleoprotein
OCLN occludin
OVOL2 ovo-like zinc finger 2
PLG plasminogen
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SEMA4A sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4A
SLURP1 secreted LY6/PLAUR domain containing 1
TINF2 TERF1 (TRF1)-interacting nuclear factor 2
TRPM8 transient receptor potential cation channel, subfamily M, member 8