







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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YFR034C | PHO4 | SGDID:S000001930 | TAL1 BHLHA17 SCL TCL5 |
T-cell acute lymphocytic leukemia protein 1 (TAL-1) (Class A basic helix-loop-helix protein 17) (bHLHa17) (Stem cell protein) (T-cell leukemia/lymphoma protein 5) |
Homo sapiens | Childhood T-Cell Acute Lymphoblastic Leukemia,Lymphoblastic Lymphoma,Leukemia, Chronic Myeloid,T-Cell Lymphoblastic Leukemia/Lymphoma,Leukemia,Acute Leukemia,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Precursor T-Cell Acute Lymphoblastic Leukemia,Diamond-Blackfan Anemia,T-Cell Acute Lymphoblastic Leukemia,Immunodeficiency 18,Lymphoma, Non-Hodgkin, Familial,Lymphoma |
2ypa_a | P17542 | ENSG00000162367 | TAL1 | 98.10 | 9.80E-10 | 1.00E-13 | 80.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFR034C | PHO4 | SGDID:S000001930 | MYC2 BHLH6 EN38 JAI1 JIN1 RAP1 RD22BP1 ZBF1 At1g32640 F6N18.4 |
Transcription factor MYC2 (AtMYC2) (Basic helix-loop-helix protein 6) (AtbHLH6) (bHLH 6) (Protein JASMONATE INSENSITIVE 1) (R-homologous Arabidopsis protein 1) (RAP-1) (Transcription factor EN 38) (Z-box binding factor 1 protein) (bHLH transcription factor bHLH006) (rd22BP1) |
Arabidopsis thaliana | 5gnj_b | Q39204 | 97.60 | 2.50E-08 | 2.80E-12 | 70.90 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
YFR034C | PHO4 | SGDID:S000001930 | TCF4 BHLHB19 ITF2 SEF2 |
Transcription factor 4 (TCF-4) (Class B basic helix-loop-helix protein 19) (bHLHb19) (Immunoglobulin transcription factor 2) (ITF-2) (SL3-3 enhancer factor 2) (SEF-2) |
Homo sapiens | Fuchs' Endothelial Dystrophy,Constipation,Angelman Syndrome,Diencephalic Astrocytoma,Intratubular Embryonal Carcinoma,Corneal Dystrophy,Subglottis Benign Neoplasm,Type 1 Diabetes Mellitus 6,Epididymis Cancer,Epididymis Adenocarcinoma,Eye Disease,Corneal Dystrophy, Fuchs Endothelial, 3,Exudative Vitreoretinopathy 7,Colorectal Cancer,Hepatocellular Carcinoma,Microcephaly,Blastic Plasmacytoid Dendritic Cell,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Cholangitis, Primary Sclerosing,Diencephalic Neoplasm,Pitt-Hopkins Syndrome,Schizophrenia,Epicanthus,Syndromic Intellectual Disability,Non-Syndromic Intellectual Disability,Deafness, X-Linked 2,Autosomal Dominant Non-Syndromic Intellectual Disability,Rett Syndrome,Autism |
6od3_h | P15884 | ENSG00000196628 | TCF4 | 97.80 | 1.00E-08 | 1.30E-12 | 66.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFR034C | PHO4 | SGDID:S000001930 | MXD1 MAD |
Max dimerization protein 1 (Max dimerizer 1) (Protein MAD) |
Homo sapiens | Williams-Beuren Syndrome |
1nlw_d | Q05195 | ENSG00000059728 | MXD1 | 97.60 | 3.40E-08 | 4.00E-12 | 67.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFR034C | PHO4 | SGDID:S000001930 | Myod1 Myod |
Myoblast determination protein 1 |
Mus musculus | 1mdy_d | P10085 | 97.80 | 7.90E-09 | 9.70E-13 | 66.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YFR034C | PHO4 | SGDID:S000001930 | ID2 BHLHB26 |
DNA-binding protein inhibitor ID-2 (Class B basic helix-loop-helix protein 26) (bHLHb26) (Inhibitor of DNA binding 2) (Inhibitor of differentiation 2) |
Homo sapiens | Neuroblastoma,Inner Ear Disease,Diamond-Blackfan Anemia,Burkitt Lymphoma,Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease,Hydronephrosis,Lujo Hemorrhagic Fever,Ewing Sarcoma,Rett Syndrome |
4aya_a | Q02363 | ENSG00000115738 | ID2 | 98.40 | 8.90E-11 | 8.90E-15 | 89.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFR034C | PHO4 | SGDID:S000001930 | SREBF1 BHLHD1 SREBP1 |
Sterol regulatory element-binding protein 1 (SREBP-1) (Class D basic helix-loop-helix protein 1) (bHLHd1) (Sterol regulatory element-binding transcription factor 1) [Cleaved into: Processed sterol regulatory element-binding protein 1 (Transcription factor SREBF1)] |
Homo sapiens | Liver Disease,Glucose Metabolism Disease,Non-Alcoholic Fatty Liver Disease,Familial Hyperlipidemia,Mucoepithelial Dysplasia, Hereditary,Overnutrition,Inherited Metabolic Disorder,Diabetes Mellitus,Fatty Liver Disease,Lipid Storage Disease,Hyperinsulinism,Leptin Deficiency Or Dysfunction,Acquired Lipodystrophy,Choline Deficiency Disease,Ichthyosis Follicularis Atrichia Photophobia Syndrome,Familial Hypercholesterolemia,Lipid Metabolism Disorder,Lysosomal Storage Disease,Prostate Cancer,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Smith-Magenis Syndrome,Familial Partial Lipodystrophy,Congenital Generalized Lipodystrophy,Hepatocellular Adenoma,Hypertension, Essential,Ifap Syndrome 1, With Or Without Bresheck Syndrome,Acquired Metabolic Disease,Lipodystrophy, Familial Partial, Type 2,Ifap Syndrome 2,Fetal Akinesia Deformation Sequence 1 |
1am9_a | P36956 | 98.40 | 6.00E-11 | 5.80E-15 | 88.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YFR034C | PHO4 | SGDID:S000001930 | SREBF1 BHLHD1 SREBP1 |
Sterol regulatory element-binding protein 1 (SREBP-1) (Class D basic helix-loop-helix protein 1) (bHLHd1) (Sterol regulatory element-binding transcription factor 1) [Cleaved into: Processed sterol regulatory element-binding protein 1 (Transcription factor SREBF1)] |
Homo sapiens | Liver Disease,Glucose Metabolism Disease,Non-Alcoholic Fatty Liver Disease,Familial Hyperlipidemia,Mucoepithelial Dysplasia, Hereditary,Overnutrition,Inherited Metabolic Disorder,Diabetes Mellitus,Fatty Liver Disease,Lipid Storage Disease,Hyperinsulinism,Leptin Deficiency Or Dysfunction,Acquired Lipodystrophy,Choline Deficiency Disease,Ichthyosis Follicularis Atrichia Photophobia Syndrome,Familial Hypercholesterolemia,Lipid Metabolism Disorder,Lysosomal Storage Disease,Prostate Cancer,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Smith-Magenis Syndrome,Familial Partial Lipodystrophy,Congenital Generalized Lipodystrophy,Hepatocellular Adenoma,Hypertension, Essential,Ifap Syndrome 1, With Or Without Bresheck Syndrome,Acquired Metabolic Disease,Lipodystrophy, Familial Partial, Type 2,Ifap Syndrome 2,Fetal Akinesia Deformation Sequence 1 |
1am9_c | P36956 | ENSG00000072310 | SREBF1 | 97.60 | 3.90E-08 | 4.60E-12 | 67.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFR034C | PHO4 | SGDID:S000001930 | Neurod1 Neurod |
Neurogenic differentiation factor 1 (NeuroD1) (Beta-cell E-box transcriptional activator 2) (Beta2) |
Mus musculus | 2ql2_b | Q60867 | 98.00 | 1.70E-09 | 2.10E-13 | 70.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YFR034C | PHO4 | SGDID:S000001930 | TCF3 BHLHB21 E2A ITF1 |
Transcription factor E2-alpha (Class B basic helix-loop-helix protein 21) (bHLHb21) (Immunoglobulin enhancer-binding factor E12/E47) (Immunoglobulin transcription factor 1) (Kappa-E2-binding factor) (Transcription factor 3) (TCF-3) (Transcription factor ITF-1) |
Homo sapiens | Saethre-Chotzen Syndrome,Childhood Acute Lymphocytic Leukemia,Retinitis Pigmentosa,Neuritis,Tafro Syndrome,Plasma Cell Neoplasm,B-Lymphoblastic Leukemia/Lymphoma,B-Lymphoblastic Leukemia/Lymphoma With Hypodiploidy,Leukemia,Childhood Leukemia,Acute Leukemia,Leukemia, Acute Myeloid,Leukemia, Acute Lymphoblastic,Agammaglobulinemia,Adult Acute Lymphocytic Leukemia,Colorectal Cancer,Agammaglobulinemia, Non-Bruton Type,Leukemia, Acute Lymphoblastic 3,Hemophagocytic Lymphohistiocytosis, Familial, 2,Pitt-Hopkins Syndrome,Alveolar Soft Part Sarcoma,Agammaglobulinemia 8, Autosomal Dominant,Myeloma, Multiple |
3u5v_a | P15923 | ENSG00000071564 | TCF3 | 97.80 | 6.50E-09 | 7.50E-13 | 71.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFR034C | PHO4 | SGDID:S000001930 | HES1 BHLHB39 HL HRY |
Transcription factor HES-1 (Class B basic helix-loop-helix protein 39) (bHLHb39) (Hairy and enhancer of split 1) (Hairy homolog) (Hairy-like protein) (hHL) |
Homo sapiens | T-Cell Lymphoblastic Leukemia/Lymphoma,Breast Cancer,Maturity-Onset Diabetes Of The Young,Medulloblastoma,3-Methylglutaconic Aciduria, Type Iii |
2mh3_b | Q14469 | ENSG00000114315 | HES1 | 97.50 | 4.90E-08 | 5.90E-12 | 64.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFR034C | PHO4 | SGDID:S000001930 | Tcf3 Alf2 Me2 Tcfe2a |
Transcription factor E2-alpha (Immunoglobulin enhancer-binding factor E12/E47) (Transcription factor 3) (TCF-3) (Transcription factor A1) |
Mus musculus | 2ql2_a | P15806 | 97.80 | 7.90E-09 | 9.60E-13 | 66.70 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YFR034C | PHO4 | SGDID:S000001930 | ID3 1R21 BHLHB25 HEIR1 |
DNA-binding protein inhibitor ID-3 (Class B basic helix-loop-helix protein 25) (bHLHb25) (Helix-loop-helix protein HEIR-1) (ID-like protein inhibitor HLH 1R21) (Inhibitor of DNA binding 3) (Inhibitor of differentiation 3) |
Homo sapiens | Burkitt Lymphoma,Lujo Hemorrhagic Fever,Fibrodysplasia Ossificans Progressiva,Rett Syndrome |
2lfh_b | Q02535 | ENSG00000117318 | ID3 | 97.80 | 1.30E-08 | 1.30E-12 | 73.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YFR034C | PHO4 | SGDID:S000001930 | CLOCK BHLHE8 KIAA0334 |
Circadian locomoter output cycles protein kaput (hCLOCK) (EC 2.3.1.48) (Class E basic helix-loop-helix protein 8) (bHLHe8) |
2.3.1.48 | Homo sapiens | Narcolepsy,Cluster Headache,Major Depressive Disorder,Sleep Disorder,Bile Duct Cystadenoma,Eating Disorder,Breast Cancer,Bipolar Disorder,Mood Disorder,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Mental Depression,Advanced Sleep Phase Syndrome, Familial, 1,Schizophrenia,Smith-Magenis Syndrome,Restless Legs Syndrome,Delayed Sleep Phase Disorder,Advanced Sleep Phase Syndrome,Attention Deficit-Hyperactivity Disorder |
4h10_b | O15516 | ENSG00000134852 | CLOCK | 97.90 | 3.50E-09 | 4.00E-13 | 72.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YFR034C | PHO4 | SGDID:S000001930 | MAX BHLHD4 |
Protein max (Class D basic helix-loop-helix protein 4) (bHLHd4) (Myc-associated factor X) |
Homo sapiens | Renal Oncocytoma,Peripheral Nervous System Benign Neoplasm,Autonomic Nervous System Benign Neoplasm,Malignant Pheochromocytoma,Esophagus Leiomyoma,Inherited Cancer-Predisposing Syndrome,Hereditary Paraganglioma-Pheochromocytoma Syndromes,Pheochromocytoma,Multiple Endocrine Neoplasia, Type Iia,Sweeney-Cox Syndrome,Tumor Predisposition Syndrome,Paraganglioma,Cutaneous Telangiectasia And Cancer Syndrome, Familial,Williams-Beuren Syndrome,Persistent Generalized Lymphadenopathy,Lung Cancer |
1hlo_a | P61244 | ENSG00000125952 | MAX | 97.60 | 2.20E-08 | 2.60E-12 | 67.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |