flat cornea Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description NT MGI. (Human Disease Ontology, DOID_0060287)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0007720
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Genes

12 genes associated with the flat cornea phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADAMTSL4 ADAMTS-like 4
BAZ1B bromodomain adjacent to zinc finger domain, 1B
CLIP2 CAP-GLY domain containing linker protein 2
ELN elastin
FBN1 fibrillin 1
GTF2I general transcription factor IIi
GTF2IRD1 GTF2I repeat domain containing 1
KERA keratocan
LIMK1 LIM domain kinase 1
PRDM5 PR domain containing 5
RFC2 replication factor C (activator 1) 2, 40kDa
TBL2 transducin (beta)-like 2