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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YIL036W | CST6 | SGDID:S000001298 | ATF4 CREB2 TXREB |
Cyclic AMP-dependent transcription factor ATF-4 (cAMP-dependent transcription factor ATF-4) (Activating transcription factor 4) (Cyclic AMP-responsive element-binding protein 2) (CREB-2) (cAMP-responsive element-binding protein 2) (Tax-responsive enhancer element-binding protein 67) (TaxREB67) |
Homo sapiens | Liver Disease,Retinitis Pigmentosa,Prion Disease,Fatty Liver Disease,Alzheimer Disease,T-Cell Lymphoblastic Leukemia/Lymphoma,Leukodystrophy,Epiphyseal Dysplasia, Multiple, With Early-Onset Diabetes Mellitus,Prostate Cancer,Leukoencephalopathy With Vanishing White Matter,Schizophrenia 1,Coffin-Lowry Syndrome |
1ci6_a | P18848 | ENSG00000128272 | ATF4 | 98.10 | 6.80E-10 | 8.40E-14 | 77.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL036W | CST6 | SGDID:S000001298 | FOS G0S7 |
Proto-oncogene c-Fos (Cellular oncogene fos) (G0/G1 switch regulatory protein 7) |
Homo sapiens | Bone Remodeling Disease,Liver Disease,Agnosia,Bone Resorption Disease,Endometrial Cancer,Autosomal Dominant Polycystic Kidney Disease,Diamond-Blackfan Anemia 5,Retinitis Pigmentosa,Migraine With Or Without Aura 1,Kagami-Ogata Syndrome,Status Epilepticus,Childhood Absence Epilepsy,Polycystic Kidney Disease,Motion Sickness,Ocular Hypertension,Myositis Ossificans,Retrograde Amnesia,Teeth Hard Tissue Disease,T-Cell Lymphoblastic Leukemia/Lymphoma,Amelogenesis Imperfecta,Van Maldergem Syndrome 1,Histiocytoid Hemangioma,Patulous Eustachian Tube,Cyclotropia,Space Motion Sickness,Malt Worker'S Lung,Colon Adenocarcinoma,Neuroblastoma,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Opiate Dependence,Morphine Dependence,Dilated Cardiomyopathy,Fumarate Hydratase Deficiency,Von Economo'S Disease,Arthritis,Anterograde Amnesia,Sleep Disorder,Exocervical Carcinoma,Osteoporosis,Femoral Cancer,Ovarian Cancer,Osteopetrosis,Trigeminal Nerve Disease,Breast Cancer,Microphthalmia,Colorectal Cancer,Peripheral Nervous System Disease,Hepatocellular Carcinoma,Vestibular Nystagmus,Occlusion Precerebral Artery,Pheochromocytoma,Cerebral Hypoxia,Amnestic Disorder,Macular Degeneration, Age-Related, 14,Embryonal Carcinoma,Bipolar Disorder,Sarcoma,Pertussis,Fibrosarcoma,Schaaf-Yang Syndrome,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Cone-Rod Dystrophy 2,Cholera,Prostate Cancer,Disease Of Mental Health,Hypercholesterolemia, Familial, 4,Rheumatoid Arthritis,Developmental And Epileptic Encephalopathy 24,Schizophrenia,Esophageal Cancer,Congenital Generalized Lipodystrophy,Inflammatory Bowel Disease,Fibrodysplasia Ossificans Progressiva,Immune Deficiency Disease,Kaufman Oculocerebrofacial Syndrome,Trigeminal Neuralgia,Hematuria, Benign Familial,Acute Promyelocytic Leukemia,Coffin-Lowry Syndrome,Vitreoretinopathy, Neovascular Inflammatory,Attention Deficit-Hyperactivity Disorder,Withdrawal Disorder,Hypertension, Essential,Specific Developmental Disorder,Estrogen-Receptor Negative Breast Cancer,Osteoblastoma,Pain Agnosia,Cardiomyopathy, Familial Hypertrophic, 25,Wilson-Turner X-Linked Mental Retardation Syndrome,Amelogenesis Imperfecta, Type Ig,Paine Syndrome,Glucocorticoid-Induced Osteoporosis,Central Hypoventilation Syndrome, Congenital,Lung Cancer,Osteogenic Sarcoma,Osteoid Osteoma |
1a02_f | P01100 | ENSG00000170345 | FOS | 97.80 | 7.50E-09 | 9.60E-13 | 69.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL036W | CST6 | SGDID:S000001298 | JUND |
Transcription factor jun-D |
Homo sapiens | T-Cell Lymphoblastic Leukemia/Lymphoma,Ovarian Cancer,Multiple Endocrine Neoplasia, Type I,Adult T-Cell Leukemia |
5vpc_b | P17535 | ENSG00000130522 | JUND | 98.40 | 4.80E-11 | 6.20E-15 | 83.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL036W | CST6 | SGDID:S000001298 | bZIP_Maf |
bZIP Maf transcription factor |
pfam Coiled | PF03131 | 97.70 | 1.60E-08 | 2.00E-12 | 75.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
YIL036W | CST6 | SGDID:S000001298 | Cebpa |
CCAAT/enhancer-binding protein alpha (C/EBP alpha) |
Rattus norvegicus | 1nwq_a | P05554 | 98.00 | 1.70E-09 | 2.00E-13 | 76.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL036W | CST6 | SGDID:S000001298 | Mafb Krml Maf1 |
Transcription factor MafB (Maf-B) (Kreisler) (Segmentation protein Kr) (Transcription factor Maf-1) (V-maf musculoaponeurotic fibrosarcoma oncogene homolog B) |
Mus musculus | 2wt7_b | P54841 | 97.70 | 1.60E-08 | 1.60E-12 | 79.60 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YIL036W | CST6 | SGDID:S000001298 | JUN |
Viral jun-transforming protein (v-Jun) |
Avian sarcoma | 2h7h_a | P05411 | 98.20 | 2.70E-10 | 3.60E-14 | 77.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YIL036W | CST6 | SGDID:S000001298 | Cebpb |
CCAAT/enhancer-binding protein beta (C/EBP beta) (AGP/EBP) (Interleukin-6-dependent-binding protein) (IL-6DBP) (Liver-enriched transcriptional activator) (LAP) |
Mus musculus | 1ci6_b | P28033 | 98.10 | 8.60E-10 | 1.10E-13 | 77.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YIL036W | CST6 | SGDID:S000001298 | Fos |
Proto-oncogene c-Fos (Cellular oncogene fos) |
Mus musculus | 2wt7_a | P01101 | 98.20 | 2.50E-10 | 3.30E-14 | 78.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YIL036W | CST6 | SGDID:S000001298 | CEBPB TCF5 PP9092 |
CCAAT/enhancer-binding protein beta (C/EBP beta) (Liver activator protein) (LAP) (Liver-enriched inhibitory protein) (LIP) (Nuclear factor NF-IL6) (Transcription factor 5) (TCF-5) |
Homo sapiens | Leukemia, Chronic Myeloid,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Burkitt Lymphoma,Myxoid Liposarcoma,Juvenile Polyposis Syndrome,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Retinoblastoma,Congenital Generalized Lipodystrophy,Immune Deficiency Disease,Ehlers-Danlos Syndrome, Spondylodysplastic Type, 3,Acute Promyelocytic Leukemia,Syndromic X-Linked Intellectual Disability Type 10,Mosaic Variegated Aneuploidy Syndrome 1 |
1h89_a | P17676 | ENSG00000172216 | CEBPB | 98.20 | 2.40E-10 | 2.90E-14 | 80.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL036W | CST6 | SGDID:S000001298 | Mafg |
Transcription factor MafG (V-maf musculoaponeurotic fibrosarcoma oncogene homolog G) |
Mus musculus | 3a5t_a | O54790 | 97.90 | 5.70E-09 | 6.40E-13 | 82.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YIL036W | CST6 | SGDID:S000001298 | ATF2 CREB2 CREBP1 |
Cyclic AMP-dependent transcription factor ATF-2 (cAMP-dependent transcription factor ATF-2) (Activating transcription factor 2) (Cyclic AMP-responsive element-binding protein 2) (CREB-2) (cAMP-responsive element-binding protein 2) (HB16) (cAMP response element-binding protein CRE-BP1) |
Homo sapiens | Autosomal Dominant Polycystic Kidney Disease,T-Cell Lymphoblastic Leukemia/Lymphoma,Eccrine Porocarcinoma,Breast Cancer,Retinoblastoma,Cardiomyopathy, Familial Hypertrophic, 25 |
1t2k_d | P15336 | ENSG00000115966 | ATF2 | 98.00 | 2.20E-09 | 2.90E-13 | 72.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL036W | CST6 | SGDID:S000001298 | JUN |
Transcription factor AP-1 (Activator protein 1) (AP1) (Proto-oncogene c-Jun) (V-jun avian sarcoma virus 17 oncogene homolog) (p39) |
Homo sapiens | Cystitis,Endometrial Cancer,Autosomal Dominant Polycystic Kidney Disease,Hyperglycemia,Retinitis Pigmentosa,Lung Cancer Susceptibility 3,Status Epilepticus,Non-Alcoholic Fatty Liver Disease,Polycystic Kidney Disease,Optic Nerve Disease,Pyriform Sinus Cancer,Melanoma,Ocular Hypertension,Hypertrophic Cardiomyopathy,Hepatoblastoma,Avian Influenza,Glottis Squamous Cell Carcinoma,Primary Cutaneous T-Cell Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Amelogenesis Imperfecta,Brain Edema,Colon Adenocarcinoma,Neuroblastoma,Familial Febrile Seizures,Leukemia, Acute Myeloid,Cystic Fibrosis,Basal Cell Carcinoma,Leukemia, Acute Lymphoblastic,Combined Immunodeficiency,Human T-Cell Leukemia Virus Type 1,Arthritis,Monocytic Leukemia,Pneumoconiosis,Nervous System Disease,Osteoporosis,Cockayne Syndrome,Cystic Kidney Disease,Ovarian Cancer,Early Yaws,Esophageal Adenosquamous Carcinoma,Breast Cancer,Squamous Cell Carcinoma, Head And Neck,Campylobacteriosis,Parkinson Disease, Late-Onset,Colorectal Cancer,Peripheral Nervous System Disease,Hepatocellular Carcinoma,Skin Benign Neoplasm,Skin Papilloma,Pheochromocytoma,Tropical Spastic Paraparesis,Hypoxia,Leukoregulin,Teratocarcinoma,Embryonal Carcinoma,Sarcoma,Pertussis,Respiratory Failure,Fibrosarcoma,Skin Carcinoma,Gastric Cancer,Cone-Rod Dystrophy 2,Prostate Cancer,Disease Of Mental Health,Toxic Encephalopathy,Body Mass Index Quantitative Trait Locus 11,Bernard-Soulier Syndrome,Pulmonary Fibrosis, Idiopathic,Retinoblastoma,Rheumatoid Arthritis,Theileriasis,Kunjin Encephalitis,Esophageal Cancer,Inflammatory Bowel Disease,Immune Deficiency Disease,Anaplastic Large Cell Lymphoma,Krabbe Disease,Hemorrhagic Cystitis,Acute Promyelocytic Leukemia,Renal Cell Carcinoma, Nonpapillary,Nasopharyngeal Carcinoma,Hypertension, Essential,Cardiomyopathy, Familial Hypertrophic, 25,Amelogenesis Imperfecta, Type Ig,Myeloma, Multiple,Medulloblastoma,Recessive Dystrophic Epidermolysis Bullosa,Salmonellosis,Lung Cancer,Helicobacter Pylori Infection,Osteogenic Sarcoma,Asthma,Pancreatic Cancer |
1jnm_a | P05412 | ENSG00000177606 | JUN | 98.20 | 2.70E-10 | 3.60E-14 | 77.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL036W | CST6 | SGDID:S000001298 | FOSB G0S3 |
Protein fosB (G0/G1 switch regulatory protein 3) |
Homo sapiens | Malignant Epithelioid Hemangioendothelioma,Bestiality,Proliferative Fasciitis,Ischemic Fasciitis,Histiocytoid Hemangioma,Hemangioma,Hemangioendothelioma,Disease Of Mental Health,Endosteal Hyperostosis, Autosomal Dominant,Osteoblastoma |
5vpe_a | P53539 | ENSG00000125740 | FOSB | 98.40 | 7.20E-11 | 9.30E-15 | 82.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YIL036W | CST6 | SGDID:S000001298 | BZLF1 |
Trans-activator protein BZLF1 (EB1) (Zebra) |
Epstein Barr | 2c9l_y | P03206 | 98.10 | 8.70E-10 | 9.90E-14 | 79.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |