Thiel-Behnke Corneal Dystrophy Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Thiel-Behnke corneal dystrophy (TBCD) is a rare form of superficial corneal dystrophy characterized by sub-epithelial honeycomb-shaped corneal opacities in the superficial cornea, and progressive visual impairment. (Orphanet Rare Disease Ontology, Orphanet_98960)
External Link https://www.disgenet.org/browser/0/1/0/C1562894
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Genes

11 genes associated with the disease Thiel-Behnke Corneal Dystrophy in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACOT8 acyl-CoA thioesterase 8
AZI2 5-azacytidine induced 2
C9ORF156 chromosome 9 open reading frame 156
COL17A1 collagen, type XVII, alpha 1
CXCL8 chemokine (C-X-C motif) ligand 8
NAA25 N(alpha)-acetyltransferase 25, NatB auxiliary subunit
NAP1L1 nucleosome assembly protein 1-like 1
NAPSA napsin A aspartic peptidase
NCKAP1 NCK-associated protein 1
TAB3 TGF-beta activated kinase 1/MAP3K7 binding protein 3
TGFBI transforming growth factor, beta-induced, 68kDa