Overlap Connective Tissue Disease Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1858556
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Genes

34 genes associated with the disease Overlap Connective Tissue Disease in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
AHR aryl hydrocarbon receptor
ANK1 ankyrin 1, erythrocytic
ANKH ANKH inorganic pyrophosphate transport regulator
AR androgen receptor
ARSB arylsulfatase B
CALCR calcitonin receptor
CNR1 cannabinoid receptor 1 (brain)
COL1A1 collagen, type I, alpha 1
CRK v-crk avian sarcoma virus CT10 oncogene homolog
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1
DKK1 dickkopf WNT signaling pathway inhibitor 1
EPAS1 endothelial PAS domain protein 1
F2R coagulation factor II (thrombin) receptor
FBN1 fibrillin 1
FERMT2 fermitin family member 2
FGF21 fibroblast growth factor 21
FGFR1 fibroblast growth factor receptor 1
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
LEP leptin
LRP5 low density lipoprotein receptor-related protein 5
MBTPS1 membrane-bound transcription factor peptidase, site 1
NEGR1 neuronal growth regulator 1
PGR progesterone receptor
S1PR3 sphingosine-1-phosphate receptor 3
SIRT1 sirtuin 1
SLIT3 slit homolog 3 (Drosophila)
SMURF1 SMAD specific E3 ubiquitin protein ligase 1
SMURF2 SMAD specific E3 ubiquitin protein ligase 2
SOST sclerostin
TPO thyroid peroxidase
WNT11 wingless-type MMTV integration site family, member 11
WNT3 wingless-type MMTV integration site family, member 3