| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YKL020C | SPT23 | SGDID:S000001503 | NFATC4 NFAT3 |
Nuclear factor of activated T-cells, cytoplasmic 4 (NF-ATc4) (NFATc4) (T-cell transcription factor NFAT3) (NF-AT3) |
Homo sapiens | Rasopathy,Dilated Cardiomyopathy,Leukostasis,Noonan Syndrome With Multiple Lentigines,Crouzon Syndrome With Acanthosis Nigricans |
2yrp_a | Q14934 | ENSG00000100968 | NFATC4 | 96.80 | 2.10E-06 | 2.20E-10 | 75.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YKL020C | SPT23 | SGDID:S000001503 | EBF3 COE3 |
Transcription factor COE3 (Early B-cell factor 3) (EBF-3) (Olf-1/EBF-like 2) (O/E-2) (OE-2) |
Homo sapiens | Renal Tubular Dysgenesis,Moebius Syndrome,Cohen Syndrome,Constipation,Neurogenic Bladder,Anus Benign Neoplasm,Urinary Tract Infection,Hereditary Melanoma,Hypotonia, Ataxia, And Delayed Development Syndrome,Griscelli Syndrome, Type 3,Familial Vesicoureteral Reflux,Renal Dysplasia,Isolated Pierre Robin Sequence,Hypotonia,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Urinary Tract Infections, Recurrent,Acid-Labile Subunit Deficiency,Urofacial Syndrome 1,Otospondylomegaepiphyseal Dysplasia, Autosomal Dominant,Renal Hypodysplasia/Aplasia 1,Vesicoureteral Reflux 1,Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital Syndrome,Ataxia And Polyneuropathy, Adult-Onset,Pierre Robin Syndrome |
3muj_b | Q9H4W6 | ENSG00000108001 | EBF3 | 98.70 | 1.70E-12 | 2.00E-16 | 115.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YKL020C | SPT23 | SGDID:S000001503 | CAMTA1 KIAA0833 MSTP023 |
Calmodulin-binding transcription activator 1 |
Homo sapiens | Cerebellar Ataxia, Nonprogressive, With Mental Retardation,Vascular Cancer,Malignant Hemangioma,Malignant Epithelioid Hemangioendothelioma,Dystonia 11, Myoclonic,Telangiectatic Osteogenic Sarcoma,Conventional Angiosarcoma,Proliferative Fasciitis,Histiocytoid Hemangioma,Neuroblastoma,Epithelioid Hemangioendothelioma,Hemangioendothelioma,Mediastinal Mesenchymal Tumor,Hepatocellular Carcinoma,Oligodendroglioma,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Brain Malformations With Or Without Urinary Tract Defects,Angiosarcoma,Chromosome 1p36 Deletion Syndrome |
2cxk_a | Q9Y6Y1 | ENSG00000171735 | CAMTA1 | 96.20 | 1.90E-05 | 2.60E-09 | 60.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |