Skin Fold (Abnormality) Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1399793
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Genes

21 genes associated with the disease Skin Fold (Abnormality) in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADIPOQ adiponectin, C1Q and collagen domain containing
ADIPOR1 adiponectin receptor 1
ANGPT1 angiopoietin 1
CD14 CD14 molecule
CD36 CD36 molecule (thrombospondin receptor)
CDON cell adhesion associated, oncogene regulated
CXCL9 chemokine (C-X-C motif) ligand 9
FAT1 FAT atypical cadherin 1
FOXL2 forkhead box L2
IL6 interleukin 6
LMNA lamin A/C
LPO lactoperoxidase
MAPRE2 microtubule-associated protein, RP/EB family, member 2
MC4R melanocortin 4 receptor
MC5R melanocortin 5 receptor
PPP1R2P9 protein phosphatase 1, regulatory (inhibitor) subunit 2 pseudogene 9
PTPN11 protein tyrosine phosphatase, non-receptor type 11
TECR trans-2,3-enoyl-CoA reductase
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor
XIAP X-linked inhibitor of apoptosis, E3 ubiquitin protein ligase