Yeast Systematic Name | Yeast Symbol | SGDID | Analog Name | Analog Description | EC | Organism | Disease | Structure | Uniprot | Human ID | Human Symbol | HHsearch Probability | HHsearch E_value | HHsearch P_value | HHsearch Score | Flag Disease related | Flag Homo sapiens | Flag Mus musculus | Flag Danio rerio | Flag Drosophila melanogaster | Flag Caenorhabditis elegans | Flag Arabidopsis thaliana | Flag Escherichia coli |
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YLR001C | YLR001C | SGDID:S000003991 | TGFBI BIGH3 |
Transforming growth factor-beta-induced protein ig-h3 (Beta ig-h3) (Kerato-epithelin) (RGD-containing collagen-associated protein) (RGD-CAP) |
Homo sapiens | Lattice Corneal Dystrophy,Recurrent Corneal Erosion,Corneal Deposit,Fuchs' Endothelial Dystrophy,Lung Cancer Susceptibility 3,Amyloidosis,Amyloidosis, Finnish Type,Corneal Dystrophy, Reis-Bucklers Type,Corneal Endothelial Dystrophy,Corneal Dystrophy, Lattice Type Iiia,Macular Dystrophy, Corneal,Granular Corneal Dystrophy,Corneal Degeneration,Interstitial Keratitis,Ocular Hyperemia,Corneal Dystrophy,Stromal Corneal Dystrophy,Corneal Disease,Keratoconus,Corneal Dystrophy, Thiel-Behnke Type,Eye Disease,Irregular Astigmatism,Corneal Edema,Corneal Ectasia,Schnyder Corneal Dystrophy,Corneal Dystrophy, Epithelial Basement Membrane,Corneal Dystrophy, Groenouw Type I,Corneal Dystrophy, Posterior Polymorphous, 1,Corneal Dystrophy, Meesmann, 1,Corneal Dystrophy, Lattice Type I,Epithelial Recurrent Erosion Dystrophy,Lubs X-Linked Mental Retardation Syndrome,Type 2 Diabetes Mellitus,Osteopetrosis, Autosomal Recessive 4,Osteopetrosis, Autosomal Recessive 6,Osteopetrosis, Autosomal Recessive 7,Corneal Dystrophy, Avellino Type,Corneal Dystrophy, Gelatinous Drop-Like,Epithelial And Subepithelial Dystrophy,Epithelial-Stromal Tgfbi Dystrophy,Stromal Dystrophy,Epithelial Basement Membrane Dystrophy,Anterior Segment Dysgenesis,Osteopetrosis, Autosomal Recessive 5 |
5nv6_a | Q15582 | ENSG00000120708 | TGFBI | 100.00 | 5.20E-53 | 3.90E-57 | 504.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR001C | YLR001C | SGDID:S000003991 | Fas1 CG6588 |
Fasciclin-1 (Fasciclin I) (FAS I) (FCN) |
Drosophila melanogaster | 1o70_a | P10674 | 99.60 | 2.60E-20 | 2.00E-24 | 200.40 | 0 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | ||||
YLR001C | YLR001C | SGDID:S000003991 | POSTN OSF2 |
Periostin (PN) (Osteoblast-specific factor 2) (OSF-2) |
Homo sapiens | Hypertensive Nephropathy,Heart Disease,Fibrous Dysplasia,Esophagus Carcinoma In Situ,Melorheostosis,Connective Tissue Disease,Bronchial Disease,Esophagitis,Allergic Disease,Myocardial Infarction,Hereditary Spastic Paraplegia,Corneal Dystrophy,Dilated Cardiomyopathy,Aortic Valve Disease 1,Brachydactyly, Type E1,Osteoporosis,Common Cold,Squamous Cell Carcinoma, Head And Neck,Esophagitis, Eosinophilic, 1,Pulmonary Fibrosis, Idiopathic,Craniopharyngioma,Spastic Paraplegia 3, Autosomal Dominant,Lung Cancer,Asthma,Pancreatic Cancer |
5yjg_a | Q15063 | ENSG00000133110 | POSTN | 100.00 | 1.90E-52 | 1.40E-56 | 496.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR001C | YLR001C | SGDID:S000003991 | DUF4993 |
Domain of unknown function |
pfam Family | PF16384 | 99.60 | 7.50E-20 | 5.60E-24 | 199.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |