| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YIL131C | FKH1 | SGDID:S000001393 | FOXN3 C14orf116 CHES1 |
Forkhead box protein N3 (Checkpoint suppressor 1) |
Homo sapiens | Pancreatic Gastrinoma,Ritscher-Schinzel Syndrome |
6nce_a | O00409 | ENSG00000053254 | FOXN3 | 99.80 | 1.20E-24 | 1.20E-28 | 180.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YIL131C | FKH1 | SGDID:S000001393 | FOXN1 RONU WHN |
Forkhead box protein N1 (Winged-helix transcription factor nude) |
Homo sapiens | Lymphopenia,Suppurative Otitis Media,Severe Combined Immunodeficiency,Hair Disease,Ectopic Thymus,Type C Thymoma,Ectodermal Dysplasia 5, Hair/Nail Type,Ectodermal Dysplasia 6, Hair/Nail Type,Ectodermal Dysplasia 7, Hair/Nail Type,Ectodermal Dysplasia 9, Hair/Nail Type,Thymic Dysplasia,Alopecia,Fraser Syndrome 1,Combined Immunodeficiency,T-Cell Immunodeficiency, Congenital Alopecia, And Nail Dystrophy,Ectodermal Dysplasia 4, Hair/Nail Type,Thymus Squamous Cell Carcinoma,T Cell Deficiency,Omenn Syndrome,Hypothyroidism, Thyroidal Or Athyroidal, With Spiky Hair And Cleft Palate,T-Cell Immunodeficiency With Thymic Aplasia,Digeorge Syndrome,T-Cell Lymphopenia, Infantile, With Or Without Nail Dystrophy, Autosomal Dominant,Alopecia Universalis Congenita,Anencephaly,Autism |
6el8_a | O15353 | ENSG00000109101 | FOXN1 | 99.80 | 3.90E-25 | 3.80E-29 | 182.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YIL131C | FKH1 | SGDID:S000001393 | FOXA3 HNF3G TCF3G |
Hepatocyte nuclear factor 3-gamma (HNF-3-gamma) (HNF-3G) (Fork head-related protein FKH H3) (Forkhead box protein A3) (Transcription factor 3G) (TCF-3G) |
Homo sapiens | Crigler-Najjar Syndrome, Type I,Maturity-Onset Diabetes Of The Young |
1vtn_c | P55318 | ENSG00000170608 | FOXA3 | 99.80 | 4.50E-25 | 4.40E-29 | 183.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YIL131C | FKH1 | SGDID:S000001393 | FOXK2 ILF ILF1 |
Forkhead box protein K2 (G/T-mismatch specific binding protein) (nGTBP) (Interleukin enhancer-binding factor 1) |
Homo sapiens | Lung Cancer |
1jxs_a | Q01167 | ENSG00000141568 | FOXK2 | 99.80 | 1.20E-25 | 1.20E-29 | 184.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YIL131C | FKH1 | SGDID:S000001393 | FOXC2 FKHL14 MFH1 |
Forkhead box protein C2 (Forkhead-related protein FKHL14) (Mesenchyme fork head protein 1) (MFH-1 protein) (Transcription factor FKH-14) |
Homo sapiens | Heart Disease,Diabetes Mellitus,Hypotrichosis,Hypoplastic Left Heart Syndrome,Primary Lymphedema,Cystic Lymphangioma,Cleft Lip/Palate-Ectodermal Dysplasia Syndrome,Filariasis,Cleft Palate, Isolated,Chylothorax, Congenital,Axenfeld-Rieger Syndrome,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Distichiasis,Intraocular Pressure Quantitative Trait Locus,Orofacial Cleft,Hereditary Lymphedema,Tetralogy Of Fallot,Varicose Veins,Klippel-Trenaunay-Weber Syndrome,Ptosis,Hypotrichosis-Lymphedema-Telangiectasia Syndrome,Lymphatic Malformation 5,Yellow Nail Syndrome,Lymphedema-Distichiasis Syndrome,Hennekam Syndrome,Anterior Segment Dysgenesis,Hereditary Lymphedema I,Hereditary Lymphedema Ii |
6akp_c | Q99958 | ENSG00000176692 | FOXC2 | 99.80 | 3.00E-25 | 2.90E-29 | 184.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |