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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YCR065W | HCM1 | SGDID:S000000661 | FOXP3 IPEX JM2 |
Forkhead box protein P3 (Scurfin) [Cleaved into: Forkhead box protein P3, C-terminally processed; Forkhead box protein P3 41 kDa form] |
Homo sapiens | Megacolon,Skin Melanoma,Primary Thrombocytopenia,X-Linked Recessive Disease,Lymphopenia,Conjunctivitis,Spinal Chordoma,Syphilis,Leishmaniasis,Cutaneous Leishmaniasis,Hypersplenism,Visceral Leishmaniasis,Neonatal Diabetes,Bronchial Disease,Diabetes Mellitus,Milk Allergy,Egg Allergy,Autoimmune Disease Of The Nervous System,Autoimmune Hepatitis,Dacryoadenitis,Leukocyte Disease,Chronic Mucocutaneous Candidiasis,Allergic Disease,Rhinitis,B Cell Deficiency,Common Variable Immunodeficiency,T-Cell Lymphoblastic Leukemia/Lymphoma,Nasal Cavity Disease,Thyroiditis,Filarial Elephantiasis,Primary Biliary Cholangitis,Diamond-Blackfan Anemia 1,Alopecia Areata,Lymph Node Disease,Arteriosclerosis,Pancytopenia,Relapsing-Remitting Multiple Sclerosis,Granulomatosis With Polyangiitis,Leukemia, Acute Myeloid,Orchitis,Combined Immunodeficiency,Autoimmune Disease,Rectal Disease,Gastroesophageal Reflux,Behcet Syndrome,Polyendocrinopathy,Late Congenital Syphilis,Dermatitis,Arthritis,Dermatitis Herpetiformis,Parasitic Protozoa Infectious Disease,Bronchiolitis Obliterans,Type 1 Diabetes Mellitus,Nose Disease,Diarrhea,Sezary'S Disease,Autoimmune Lymphoproliferative Syndrome,Brachydactyly, Type C,Immune System Disease,Hypersensitivity Reaction Type Iv Disease,Caplan'S Syndrome,Aplastic Anemia,Ovarian Cancer,T-Cell Adult Acute Lymphocytic Leukemia,Crohn'S Disease,Food Allergy,Parasitic Helminthiasis Infectious Disease,Breast Cancer,Colorectal Cancer,Interstitial Lung Disease,Hepatocellular Carcinoma,Autoimmune Polyendocrine Syndrome,Tropical Spastic Paraparesis,Autoimmune Enteropathy,Demyelinating Disease,Thymoma,Deficiency Anemia,Dermatitis, Atopic, 8,Dermatitis, Atopic,Bone Inflammation Disease,Allergic Conjunctivitis,Prostatitis,Skin Carcinoma,Omenn Syndrome,Uveal Disease,Cone-Rod Dystrophy 2,Disease Of Mental Health,Thrombocytopenia,Integumentary System Disease,Skin Disease,Rheumatoid Arthritis,Type 2 Diabetes Mellitus,Multiple Sclerosis,Autoimmune Pancreatitis,Autoimmune Atherosclerosis,Secretory Diarrhea,Autoimmune Polyendocrine Syndrome Type 1,Primary Bacterial Infectious Disease,Malaria,Hydrops Fetalis, Nonimmune,Hypotrichosis 1,Aneruptive Fever,Early Congenital Syphilis,Adult T-Cell Leukemia,Esophageal Cancer,Immunodeficiency 31c,Inflammatory Bowel Disease,Kawasaki Disease,Immune Deficiency Disease,Immunodeficiency 41 With Lymphoproliferation And Autoimmunity,X-Linked Monogenic Disease,Peripheral T-Cell Lymphoma,Hashimoto Thyroiditis,Leprosy 3,Spermatogenic Failure 3,Tongue Squamous Cell Carcinoma,Lymphoid Interstitial Pneumonia,Immunodysregulation, Polyendocrinopathy, And Enteropathy, X-Linked,Autoimmune Disease Of Central Nervous System,Autoimmune Disease Of Endocrine System,Autoimmune Disease Of Eyes, Ear, Nose And Throat,Autoimmune Disease Of Gastrointestinal Tract,Autoimmune Disease Of Musculoskeletal System,Autoimmune Disease Of Skin And Connective Tissue,Bone Marrow Failure Syndrome 1,Autoimmune Disease Of Blood,Colitis,Systemic Lupus Erythematosus,Mycosis Fungoides,Pollen Allergy,Autoimmune Neuropathy,Fruit Allergy,Permanent Neonatal Diabetes Mellitus,Legume Allergy,Lung Cancer,Celiac Disease 1,Asthma |
3qrf_g | Q9BZS1 | ENSG00000049768 | FOXP3 | 99.80 | 4.60E-24 | 5.30E-28 | 164.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YCR065W | HCM1 | SGDID:S000000661 | FOXO1 FKHR FOXO1A |
Forkhead box protein O1 (Forkhead box protein O1A) (Forkhead in rhabdomyosarcoma) |
Homo sapiens | Ectomesenchymoma,Breast Rhabdomyosarcoma,Muscular Disease,Endometrial Cancer,Retinitis Pigmentosa,Patau Syndrome,Primary Mediastinal B-Cell Lymphoma,Rhabdomyosarcoma 2,Diabetes Mellitus,Glioma,Leukemia, Acute Myeloid,Hepatocellular Clear Cell Carcinoma,Synovium Cancer,Osteoporosis,Burkitt Lymphoma,Glucose Intolerance,Breast Cancer,Parkinson Disease, Late-Onset,Colon Leiomyoma,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Pleomorphic Rhabdomyosarcoma,Orbit Embryonal Rhabdomyosarcoma,Orbit Rhabdomyosarcoma,Brittle Cornea Syndrome,Prostate Cancer,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Skeletal Muscle Cancer,Muscle Cancer,Central Nervous System Rhabdomyosarcoma,Sarcoma, Synovial,Ewing Sarcoma,Tuberous Sclerosis 1,Parameningeal Embryonal Rhabdomyosarcoma,Glucocorticoid-Induced Osteoporosis,Medulloblastoma,Aging,Leigh Syndrome |
3co6_c | Q12778 | ENSG00000150907 | FOXO1 | 99.80 | 5.50E-24 | 6.00E-28 | 171.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YCR065W | HCM1 | SGDID:S000000661 | 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 | 4.20E-25 | 4.80E-29 | 175.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YCR065W | HCM1 | SGDID:S000000661 | 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 | 2.80E-24 | 3.20E-28 | 172.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YCR065W | HCM1 | SGDID:S000000661 | 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 | 3.50E-25 | 4.00E-29 | 175.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YCR065W | HCM1 | SGDID:S000000661 | FOXN3 C14orf116 CHES1 |
Forkhead box protein N3 (Checkpoint suppressor 1) |
Homo sapiens | Pancreatic Gastrinoma,Ritscher-Schinzel Syndrome |
6nce_a | O00409 | ENSG00000053254 | FOXN3 | 99.80 | 4.00E-25 | 4.40E-29 | 177.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |