Gene table of TGFBI : transforming growth factor beta induced

Gene-disease associations table

Disease ID	Disease name	Source of annotation with TGFBI	OMIM link	Number of associated genes	genes
121900	CORNEAL DYSTROPHY, GROENOUW TYPE I	ClinVar, OMIM, HUMSAVAR	link to OMIM	1	TGFBI
122200	CORNEAL DYSTROPHY, LATTICE TYPE I	ClinVar, OMIM, HUMSAVAR	link to OMIM	1	TGFBI
602082	CORNEAL DYSTROPHY, THIEL-BEHNKE TYPE	ClinVar, OMIM, HUMSAVAR	link to OMIM	1	TGFBI
608470	CORNEAL DYSTROPHY, REIS-BUCKLERS TYPE	ClinVar, OMIM, HUMSAVAR	link to OMIM	1	TGFBI
607541	CORNEAL DYSTROPHY, AVELLINO TYPE	ClinVar, OMIM, HUMSAVAR	link to OMIM	1	TGFBI
121820	CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE	ClinVar, OMIM, HUMSAVAR	link to OMIM	1	TGFBI
608471	CORNEAL DYSTROPHY, LATTICE TYPE IIIA	ClinVar, OMIM, HUMSAVAR	link to OMIM	1	TGFBI

Associated genes in ENSEMBL

Associated proteins - SwissProt Accession ID

Associated PDB IDs

Cytogenetic Band

Tandem repeats annotation

Transcription regulation as annotated in TRRUST

Associated KEGG pathways

Associated REACTOME pathways

REACTOME pathway	REACTOME ID	REACTOME IC
Amyloids	R-HSA-977225	7.37
Disease	R-HSA-1643685	3.33

Associated GO terms for Molecular function

GO term	GO ID	GO IC
integrin binding	GO:0005178	5.07
cell adhesion molecule binding	GO:0050839	4.5
extracellular matrix binding	GO:0050840	5.79
macromolecular complex binding	GO:0044877	2.61
binding	GO:0005488	0.18
protein binding	GO:0005515	0.46
protein complex binding	GO:0032403	3.09
receptor binding	GO:0005102	2.43
collagen binding	GO:0005518	5.58