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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YCR065W HCM1 / SGDID:S000000661
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
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
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
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

Weizmann Institute of Science | Maya Schuldiner Lab