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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YOL067C | RTG1 | SGDID:S000005428 | Mitf Bw Mi Vit |
Microphthalmia-associated transcription factor |
Mus musculus | 4ath_a | Q08874 | 97.80 | 1.30E-08 | 1.20E-12 | 68.00 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YOL067C | RTG1 | SGDID:S000005428 | 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 | 97.90 | 5.70E-09 | 5.70E-13 | 64.20 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YOL067C | RTG1 | SGDID:S000005428 | 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 | 98.50 | 4.00E-11 | 3.40E-15 | 80.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | MYC BHLHE39 |
Myc proto-oncogene protein (Class E basic helix-loop-helix protein 39) (bHLHe39) (Proto-oncogene c-Myc) (Transcription factor p64) |
Homo sapiens | Supratentorial Cancer,Skin Melanoma,Heart Disease,Endometrial Cancer,Richter'S Syndrome,Autosomal Dominant Polycystic Kidney Disease,Blood Protein Disease,Squamous Cell Carcinoma,Lymphoblastic Lymphoma,Retinitis Pigmentosa,Thyroid Gland Cancer,Anal Carcinoma In Situ,Lung Cancer Susceptibility 3,Acquired Immunodeficiency Syndrome,Chronic Myelomonocytic Leukemia,Relapsed/Refractory Diffuse Large B-Cell Lymphoma,Adenoid Cystic Carcinoma,Polycystic Kidney Disease,Cornelia De Lange Syndrome,Vulva Basal Cell Carcinoma,Suppression Of Tumorigenicity 12,Melanoma,Leukemia, Chronic Myeloid,Fallopian Tube Carcinoma,Leiomyosarcoma,Rectum Adenocarcinoma,B-Lymphoblastic Leukemia/Lymphoma,Peripheral Nervous System Neoplasm,Uterine Corpus Cancer,Connective Tissue Cancer,Bone Sarcoma,Hypertrophic Cardiomyopathy,Hepatitis B,Frontal Lobe Neoplasm,Refractory Celiac Disease,Leukocyte Disease,Clear Cell Renal Cell Carcinoma,Plasma Cell Leukemia,Hepatoblastoma,Rasopathy,Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type,Breast Angiosarcoma,Mature B-Cell Neoplasm,B-Cell Lymphoma,Atypical Teratoid Rhabdoid Tumor,Intestinal Benign Neoplasm,Amyotrophic Lateral Sclerosis 1,Malignant Ovarian Surface Epithelial-Stromal Neoplasm,Ovary Epithelial Cancer,Plasmablastic Lymphoma,T-Cell Lymphoblastic Leukemia/Lymphoma,Ocular Cancer,Amelogenesis Imperfecta,Retinal Cancer,Essential Thrombocythemia,Biliary Tract Disease,Cerebral Primitive Neuroectodermal Tumor,Infratentorial Cancer,Pediatric Systemic Lupus Erythematosus,Monoclonal Gammopathy Of Uncertain Significance,Lymphatic System Disease,Supratentorial Primitive Neuroectodermal Tumor,Leukemia,Colon Adenocarcinoma,Neuroblastoma,Colonic Benign Neoplasm,Inflammatory Bowel Disease 28,Bile Duct Adenocarcinoma,Esophagus Adenocarcinoma,Epilepsy, Idiopathic Generalized 3,Leukemia, Acute Myeloid,Sporadic Breast Cancer,Intravascular Large B-Cell Lymphoma,Bone Marrow Cancer,High Grade B-Cell Lymphoma With Myc And/ Or Bcl2 And/Or Bcl6 Rearrangement,Leber Plus Disease,Hemangioma,Hemimegalencephaly,Leukemia, Acute Lymphoblastic,Autonomic Nervous System Neoplasm,Feingold Syndrome 1,Dilated Cardiomyopathy,Basal Cell Nevus Syndrome,Bladder Cancer,Dyskeratosis Congenita,Megaesophagus,Brain Cancer,Precursor T-Cell Acute Lymphoblastic Leukemia,Lung Adenoma,Reticulosarcoma,Sezary'S Disease,Cervix Carcinoma,Gum Cancer,Aggressive Nk-Cell Leukemia,T-Cell Prolymphocytic Leukemia,Nervous System Disease,Diamond-Blackfan Anemia,Prolymphocytic Leukemia,Ovarian Cancer,Myeloid Leukemia,Burkitt Lymphoma,Lung Giant Cell Carcinoma,Adenocarcinoma,Germ Cell Cancer,In Situ Carcinoma,Tuberous Sclerosis,Testicular Cancer,T-Cell Acute Lymphoblastic Leukemia,Eye Disease,Paranasal Sinus Lymphoma,Juvenile Nasopharyngeal Angiofibroma,Breast Carcinoma In Situ,Breast Cancer,Glioblastoma,Squamous Cell Carcinoma, Head And Neck,Actinic Keratosis,Malignant Astrocytoma,Parkinson Disease, Late-Onset,Colorectal Cancer,Peripheral Nervous System Disease,Nervous System Cancer,Germ Cell And Embryonal Cancer,Central Nervous System Hematologic Cancer,Hepatocellular Carcinoma,Pediatric Lymphoma,Adult Lymphoma,Keratoacanthoma,Skin Papilloma,Diffuse Large B-Cell Lymphoma Of The Central Nervous System,Alk-Negative Anaplastic Large Cell Lymphoma,Pheochromocytoma,Central Nervous System Lymphoma,B Cell Prolymphocytic Leukemia,Embryonal Rhabdomyosarcoma,Rhabdomyosarcoma,Blastic Plasmacytoid Dendritic Cell,Tongue Disease,Polycystic Kidney Disease 1 With Or Without Polycystic Liver Disease,Hepatic Angiomyolipoma,Sarcoma,Fanconi Anemia, Complementation Group A,Fibrosarcoma,Bone Osteosarcoma,Liposarcoma,Appendix Lymphoma,Skin Carcinoma,Gastric Cancer,Breast Adenocarcinoma,Lymphangioma,Prostate Cancer,Disease Of Mental Health,Pancreatic Ductal Adenocarcinoma,Gallbladder Signet Ring Cell Adenocarcinoma,Pancreatic Ductal Carcinoma,Cervical Cancer,Ovarian Cystadenocarcinoma,Panniculitis,Contractures, Pterygia, And Spondylocarpotarsal Fusion Syndrome 1a,Central Nervous System Cancer,Congenital Myasthenic Syndrome,Rhabdoid Cancer,Retinoblastoma,Cervical Adenocarcinoma,Ovary Adenocarcinoma,Plasmacytoma,Cervical Squamous Cell Carcinoma,Angiosarcoma,Large Cell Medulloblastoma,Childhood Medulloblastoma,Nodular Medulloblastoma,Thyroid Gland Follicular Carcinoma,Sensory System Disease,Merkel Cell Carcinoma,Lymphoma, Non-Hodgkin, Familial,Skeletal Muscle Cancer,Muscle Cancer,Ventricular Tachycardia, Catecholaminergic Polymorphic, 3,Familial Adenomatous Polyposis,Hypotrichosis 1,Adult T-Cell Leukemia,Esophageal Cancer,Epilepsy, Idiopathic Generalized 15,Inflammatory Bowel Disease,Respiratory System Benign Neoplasm,Gastrointestinal System Benign Neoplasm,Barrett Esophagus,Myelodysplastic Syndrome,Lymphoma, Mucosa-Associated Lymphoid Type,Autosomal Genetic Disease,Mature T-Cell And Nk-Cell Lymphoma,Diffuse Large B-Cell Lymphoma,Ewing Sarcoma,Mantle Cell Lymphoma,Colorectal Adenoma,Colorectal Adenocarcinoma,Acute Promyelocytic Leukemia,Follicular Lymphoma,Inflammatory Myofibroblastic Tumor,Rectum Adenoma,Nasopharyngeal Carcinoma,Wilms Tumor 1,Lymphoma,Pre-Malignant Neoplasm,Lymphatic System Cancer,Ductal Carcinoma In Situ,Estrogen-Receptor Positive Breast Cancer,Cell Type Benign Neoplasm,Kabuki Syndrome 1,Kaposi Sarcoma,Nijmegen Breakage Syndrome,Leukemia, Chronic Lymphocytic,Amelogenesis Imperfecta, Type Ig,Li-Fraumeni Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability,Pelizaeus-Merzbacher Disease,Nut Midline Carcinoma,Gingival Fibromatosis,Myeloma, Multiple,Medulloblastoma,Spinal Disease,Melanoma, Cutaneous Malignant 1,Recessive Dystrophic Epidermolysis Bullosa,Melanoma, Uveal,Spermatogenic Failure, Y-Linked, 1,Neuroblastoma 1,Retinitis Pigmentosa 11,Lung Cancer,Osteogenic Sarcoma,Pancreatic Cancer |
6g6k_a | P01106 | ENSG00000136997 | MYC | 98.60 | 6.90E-12 | 6.40E-16 | 87.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | 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 | 98.40 | 5.20E-11 | 5.20E-15 | 78.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | 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 | 99.00 | 4.80E-14 | 4.10E-18 | 98.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YOL067C | RTG1 | SGDID:S000005428 | 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 | 98.30 | 1.90E-10 | 1.80E-14 | 78.20 | 0 | 0 | 0 | 0 | 0 | 0 | 1 | 0 | ||||
YOL067C | RTG1 | SGDID:S000005428 | 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 | 98.20 | 3.80E-10 | 3.50E-14 | 78.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | SREBF2 BHLHD2 SREBP2 |
Sterol regulatory element-binding protein 2 (SREBP-2) (Class D basic helix-loop-helix protein 2) (bHLHd2) (Sterol regulatory element-binding transcription factor 2) [Cleaved into: Processed sterol regulatory element-binding protein 2 (Transcription factor SREBF2)] |
Homo sapiens | Non-Alcoholic Fatty Liver Disease,Familial Hyperlipidemia,Inherited Metabolic Disorder,Diabetes Mellitus,Dystonia, Dopa-Responsive, Due To Sepiapterin Reductase Deficiency,Lipid Storage Disease,Avascular Necrosis,Sitosterolemia,Atherosclerosis Susceptibility,Sveinsson Chorioretinal Atrophy,Familial Hypercholesterolemia,Niemann-Pick Disease,Body Mass Index Quantitative Trait Locus 11,C Syndrome,Niemann-Pick Disease, Type C1 |
1ukl_d | Q12772 | ENSG00000198911 | SREBF2 | 97.90 | 3.60E-09 | 3.60E-13 | 65.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | 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 | 8.70E-09 | 8.70E-13 | 63.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | MXD1 MAD |
Max dimerization protein 1 (Max dimerizer 1) (Protein MAD) |
Homo sapiens | Williams-Beuren Syndrome |
1nlw_d | Q05195 | ENSG00000059728 | MXD1 | 98.40 | 7.10E-11 | 7.00E-15 | 77.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | Myod1 Myod |
Myoblast determination protein 1 |
Mus musculus | 1mdy_d | P10085 | 97.80 | 9.30E-09 | 9.30E-13 | 63.50 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YOL067C | RTG1 | SGDID:S000005428 | 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 | 98.20 | 4.50E-10 | 4.00E-14 | 79.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | 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 | 98.00 | 1.60E-09 | 1.60E-13 | 70.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YOL067C | RTG1 | SGDID:S000005428 | Neurod1 Neurod |
Neurogenic differentiation factor 1 (NeuroD1) (Beta-cell E-box transcriptional activator 2) (Beta2) |
Mus musculus | 2ql2_b | Q60867 | 98.10 | 1.00E-09 | 1.00E-13 | 67.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
YOL067C | RTG1 | SGDID:S000005428 | 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 | 98.40 | 4.40E-11 | 4.30E-15 | 79.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | 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 | 5.90E-08 | 5.80E-12 | 61.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YOL067C | RTG1 | SGDID:S000005428 | 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 | 98.00 | 2.90E-09 | 2.80E-13 | 69.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |