Cornea Plana Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description NT MGI. (Human Disease Ontology, DOID_0060287)
External Link https://www.disgenet.org/browser/0/1/0/C0344529
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Genes

21 genes associated with the disease Cornea Plana in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ADAMTS2 ADAM metallopeptidase with thrombospondin type 1 motif, 2
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CLIP2 CAP-GLY domain containing linker protein 2
DCN decorin
ELN elastin
EPYC epiphycan
FBN1 fibrillin 1
FOXC1 forkhead box C1
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
KERA keratocan
LIMK1 LIM domain kinase 1
LUM lumican
MARK3 MAP/microtubule affinity-regulating kinase 3
PITX2 paired-like homeodomain 2
PPP3CB protein phosphatase 3, catalytic subunit, beta isozyme
PPP3R1 protein phosphatase 3, regulatory subunit B, alpha
RFC2 replication factor C (activator 1) 2, 40kDa
SLC7A3 solute carrier family 7 (cationic amino acid transporter, y+ system), member 3
TBL2 transducin (beta)-like 2
TGFB2 transforming growth factor, beta 2