| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YER088C | DOT6 | SGDID:S000000890 | Myb |
Transcriptional activator Myb (Proto-oncogene c-Myb) |
Mus musculus | 1guu_a | P06876 | 98.30 | 2.40E-10 | 2.40E-14 | 83.90 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YER088C | DOT6 | SGDID:S000000890 | TADA2A TADA2L KL04P |
Transcriptional adapter 2-alpha (Transcriptional adapter 2-like) (ADA2-like protein) |
Homo sapiens | Chromosome 17q12 Deletion Syndrome |
1x41_a | O75478 | ENSG00000276234 | TADA2A | 97.50 | 3.70E-08 | 5.30E-12 | 64.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER088C | DOT6 | SGDID:S000000890 | Mybl2 Bmyb |
Myb-related protein B (B-Myb) (Myb-like protein 2) |
Mus musculus | 2d9a_a | P48972 | 97.50 | 3.90E-08 | 5.60E-12 | 64.30 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YER088C | DOT6 | SGDID:S000000890 | TERF1 PIN2 TRBF1 TRF TRF1 |
Telomeric repeat-binding factor 1 (NIMA-interacting protein 2) (TTAGGG repeat-binding factor 1) (Telomeric protein Pin2/TRF1) |
Homo sapiens | Revesz Syndrome,Hoyeraal Hreidarsson Syndrome,Dyskeratosis Congenita,Aplastic Anemia,Anaplastic Astrocytoma,Werner Syndrome,Cherubism,Fanconi Anemia, Complementation Group A,Pulmonary Fibrosis, Idiopathic,Dyskeratosis Congenita, Autosomal Dominant 3,Townes-Brocks Syndrome,Meningioma, Familial,Nijmegen Breakage Syndrome,Arthrogryposis, Renal Dysfunction, And Cholestasis 1,Melanoma, Cutaneous Malignant 1,Lung Cancer |
1ba5_a | P54274 | ENSG00000147601 | TERF1 | 97.30 | 1.30E-07 | 2.00E-11 | 59.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER088C | DOT6 | SGDID:S000000890 | TERF2 TRBF2 TRF2 |
Telomeric repeat-binding factor 2 (TTAGGG repeat-binding factor 2) (Telomeric DNA-binding protein) |
Homo sapiens | Chronic Congestive Splenomegaly,Hoyeraal Hreidarsson Syndrome,Dyskeratosis Congenita,Aplastic Anemia,Werner Syndrome,Coats Disease,Nijmegen Breakage Syndrome,Melanoma, Cutaneous Malignant 1,Bloom Syndrome |
3sjm_a | Q15554 | ENSG00000132604 | TERF2 | 97.30 | 1.50E-07 | 2.20E-11 | 61.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER088C | DOT6 | SGDID:S000000890 | MYSM1 KIAA1915 |
Deubiquitinase MYSM1 (2A-DUB) (EC 3.4.19.-) (Myb-like, SWIRM and MPN domain-containing protein 1) |
3.4.19.- | Homo sapiens | Congenital Progressive Bone Marrow Failure-B-Cell Immunodeficiency-Skeletal Dysplasia Syndrome,Bone Marrow Failure Syndrome 4 |
2cu7_a | Q5VVJ2 | ENSG00000162601 | MYSM1 | 97.50 | 5.30E-08 | 7.40E-12 | 67.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YER088C | DOT6 | SGDID:S000000890 | MIS18BP1 C14orf106 KIAA1903 KNL2 M18BP1 |
Mis18-binding protein 1 (Kinetochore-associated protein KNL-2 homolog) (HsKNL-2) (P243) |
Homo sapiens | Fanconi Anemia, Complementation Group I |
1wgx_a | Q6P0N0 | ENSG00000129534 | MIS18BP1 | 97.20 | 2.20E-07 | 2.80E-11 | 66.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER088C | DOT6 | SGDID:S000000890 | Terb1 Ccdc79 |
Telomere repeats-binding bouquet formation protein 1 (Coiled-coil domain-containing protein 79) |
Mus musculus | 1x58_a | Q8C0V1 | 97.50 | 6.70E-08 | 8.50E-12 | 67.10 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | ||||
| YER088C | DOT6 | SGDID:S000000890 | SMARCC1 BAF155 |
SWI/SNF complex subunit SMARCC1 (BRG1-associated factor 155) (BAF155) (SWI/SNF complex 155 kDa subunit) (SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily C member 1) |
Homo sapiens | Spinal Meningioma,Spinal Canal And Spinal Cord Meningioma,Congenital Hydrocephalus,Atypical Teratoid Rhabdoid Tumor,Neurilemmomatosis,Hydrocephalus,Clark-Baraitser Syndrome,Rhabdoid Cancer,Kidney Rhabdoid Cancer,Autosomal Dominant Non-Syndromic Intellectual Disability |
2yus_a | Q92922 | ENSG00000173473 | SMARCC1 | 97.20 | 2.90E-07 | 3.70E-11 | 66.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER088C | DOT6 | SGDID:S000000890 | DNAJC1 HTJ1 |
DnaJ homolog subfamily C member 1 (DnaJ protein homolog MTJ1) |
Homo sapiens | Pyometritis |
2cqr_a | Q96KC8 | ENSG00000136770 | DNAJC1 | 97.60 | 2.80E-08 | 3.80E-12 | 69.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER088C | DOT6 | SGDID:S000000890 | CDC5L KIAA0432 PCDC5RP |
Cell division cycle 5-like protein (Cdc5-like protein) (Pombe cdc5-related protein) |
Homo sapiens | Cakut,Cystoisosporiasis,Renal Dysplasia,Poikiloderma With Neutropenia,Hepatic Adenomas, Familial,Peroxisomal Acyl-Coa Oxidase Deficiency |
2dim_a | Q99459 | ENSG00000096401 | CDC5L | 97.30 | 1.60E-07 | 2.20E-11 | 63.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YER088C | DOT6 | SGDID:S000000890 | ada2 SPCC24B10.08c |
Transcriptional adapter 2 |
Schizosaccharomyces pombe | 2elk_a | Q9P7J7 | 97.50 | 4.80E-08 | 6.70E-12 | 64.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |