Annotation Detail
Information
- Associated Genes
- TGFBI
- Associated Variants
-
TGFBI p.Arg124Ser (p.R124S)
(
ENST00000442011.7 )
TGFBI p.Arg124Cys (p.R124C) ( ENST00000442011.7 )
TGFBI p.Arg124His (p.R124H) ( ENST00000442011.7 )
TGFBI p.Arg124Leu (p.R124L) ( ENST00000442011.7 )
TGFBI p.Pro501Thr (p.P501T) ( ENST00000442011.7 )
TGFBI p.Pro501Ala (p.P501A) ( ENST00000442011.7 )
TGFBI p.Pro501Ser (p.P501S) ( ENST00000442011.7 )
TGFBI p.Ala546Asp (p.A546D) ( ENST00000442011.7 )
TGFBI p.Arg555Trp (p.R555W) ( ENST00000442011.7 )
TGFBI p.Arg124Ser (p.R124S) ( ENST00000442011.7 )
TGFBI p.Arg124Cys (p.R124C) ( ENST00000442011.7 )
TGFBI p.Arg124His (p.R124H) ( ENST00000442011.7 )
TGFBI p.Arg124Leu (p.R124L) ( ENST00000442011.7 )
TGFBI p.Pro501Thr (p.P501T) ( ENST00000442011.7 )
TGFBI p.Pro501Ala (p.P501A) ( ENST00000442011.7 )
TGFBI p.Pro501Ser (p.P501S) ( ENST00000442011.7 )
TGFBI p.Ala546Asp (p.A546D) ( ENST00000442011.7 )
TGFBI p.Arg555Trp (p.R555W) ( ENST00000442011.7 ) - Associated Disease
- Corneal Dystrophy, Lattice Type IIIA
- Source Database
- DisGeNET
- Description
- In our study, thirty patients from five pedigrees and ten sporadic patients were diagnosed as four TGFBI gene-linked corneal dystrophies of granular corneal dystrophy type I (GGCD I), Avellino corneal dystrophy (ACD), lattice corneal dystrophy type I (LCD I), and lattice corneal dystrophy type IIIA (LCD IIIA), and in total, seven disease-causing mutations, namely R555W, A546D, A546T, and T538P mutations in exon 12, R124H and R124C mutations in exon 4, and P501T mutation in exon 11, were identified, while four polymorphisms of V327V, L472L, F540F, and 1665-1666insC were screened in exons 8, 11, and 12.
- Pubmed
- 21462384
- Original source reporting the Gene Disease association
- BeFree
- DisGENET score for the Gene Disease association
- 0.360542883744161
- Year of publication
- 2011
Drugs