| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YBR182C | SMP1 | SGDID:S000000386 | MEF2A MEF2 |
Myocyte-specific enhancer factor 2A (Serum response factor-like protein 1) |
Homo sapiens | Heart Disease,Coronary Artery Disease, Autosomal Dominant, 1,Hypertrophic Cardiomyopathy,Myocardial Infarction,Myotonic Dystrophy 1,Ichthyosis, Congenital, Autosomal Recessive 9,Dilated Cardiomyopathy,Rhabdomyosarcoma,Muscle Hypertrophy,Lipoprotein Quantitative Trait Locus |
1egw_a | Q02078 | 99.80 | 2.00E-24 | 1.80E-28 | 168.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YBR182C | SMP1 | SGDID:S000000386 | MEF2A MEF2 |
Myocyte-specific enhancer factor 2A (Serum response factor-like protein 1) |
Homo sapiens | Heart Disease,Coronary Artery Disease, Autosomal Dominant, 1,Hypertrophic Cardiomyopathy,Myocardial Infarction,Myotonic Dystrophy 1,Ichthyosis, Congenital, Autosomal Recessive 9,Dilated Cardiomyopathy,Rhabdomyosarcoma,Muscle Hypertrophy,Lipoprotein Quantitative Trait Locus |
1egw_d | Q02078 | ENSG00000068305 | MEF2A | 99.60 | 7.50E-20 | 8.40E-24 | 136.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YBR182C | SMP1 | SGDID:S000000386 | MCM1 FUN80 YMR043W YM9532.08 |
Pheromone receptor transcription factor (GRM/PRTF protein) |
Saccharomyces cerevisiae | 1mnm_b | P11746 | 99.60 | 1.00E-19 | 1.10E-23 | 145.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YBR182C | SMP1 | SGDID:S000000386 | SRF |
Serum response factor (SRF) |
Homo sapiens | Heart Disease,Hemophagocytic Lymphohistiocytosis, Familial, 1,Myofibroma,Amyotrophic Lateral Sclerosis 1,T-Cell Lymphoblastic Leukemia/Lymphoma,Ocular Dominance,Miller Fisher Syndrome,Human T-Cell Leukemia Virus Type 1,Dilated Cardiomyopathy,Fumarate Hydratase Deficiency,Myopericytoma,Acute Megakaryocytic Leukemia,Neuronal Ceroid Lipofuscinosis,Myopathy, Myofibrillar, 9, With Early Respiratory Failure,Skin Disease,Rheumatoid Arthritis,Muscle Hypertrophy,Lymphangioleiomyomatosis,Ceroid Lipofuscinosis, Neuronal, 2,Ceroid Lipofuscinosis, Neuronal, 1 |
1hbx_d | P11831 | ENSG00000112658 | SRF | 99.70 | 2.10E-21 | 2.20E-25 | 153.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |