| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YJL047C | RTT101 | SGDID:S000003583 | CUL5 VACM1 |
Cullin-5 (CUL-5) (Vasopressin-activated calcium-mobilizing receptor 1) (VACM-1) |
Homo sapiens | Cockayne Syndrome,Molluscum Contagiosum,Cockayne Syndrome B,Lung Cancer |
3dpl_c | Q93034 | ENSG00000166266 | CUL5 | 100.00 | 1.10E-36 | 1.20E-40 | 319.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL047C | RTT101 | SGDID:S000003583 | CUL4A |
Cullin-4A (CUL-4A) |
Homo sapiens | Xeroderma Pigmentosum Group E,Cockayne Syndrome,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Complementation Group E,Xeroderma Pigmentosum, Variant Type,Pediatric Osteosarcoma,Uv-Sensitive Syndrome,Autosomal Recessive Non-Syndromic Intellectual Disability |
2hye_c | Q13619 | ENSG00000139842 | CUL4A | 100.00 | 2.10E-40 | 2.20E-44 | 378.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL047C | RTT101 | SGDID:S000003583 | CUL1 |
Cullin-1 (CUL-1) |
Homo sapiens | Xeroderma Pigmentosum Group E,Three M Syndrome 1,Ovarian Cancer,Breast Cancer,Parkinson Disease, Late-Onset,Weaver Syndrome,Vaccinia |
1ldk_b | Q13616 | ENSG00000055130 | CUL1 | 100.00 | 3.00E-37 | 3.30E-41 | 321.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL047C | RTT101 | SGDID:S000003583 | ANAPC2 APC2 KIAA1406 |
Anaphase-promoting complex subunit 2 (APC2) (Cyclosome subunit 2) |
Homo sapiens | Bardet-Biedl Syndrome 10,Mitochondrial Complex I Deficiency, Nuclear Type 1 |
5a31_n | Q9UJX6 | ENSG00000176248 | ANAPC2 | 99.90 | 7.30E-33 | 6.80E-37 | 318.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL047C | RTT101 | SGDID:S000003583 | CUL4B KIAA0695 |
Cullin-4B (CUL-4B) |
Homo sapiens | Seizure Disorder,Smith-Fineman-Myers Syndrome,Cockayne Syndrome,Alacrima, Achalasia, And Mental Retardation Syndrome,Disease Of Mental Health,Danon Disease,Mental Retardation, X-Linked, Syndromic, Cabezas Type,Pettigrew Syndrome,Autosomal Recessive Non-Syndromic Intellectual Disability,Syndromic X-Linked Intellectual Disability Cabezas Type |
4a0l_e | Q13620 | ENSG00000158290 | CUL4B | 100.00 | 1.80E-38 | 2.00E-42 | 357.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL047C | RTT101 | SGDID:S000003583 | CUL2 |
Cullin-2 (CUL-2) |
Homo sapiens | Familial Renal Papillary Carcinoma,Hereditary Renal Cell Carcinoma,Amyotrophic Lateral Sclerosis 1,Dermis Tumor,Familial Isolated Hypoparathyroidism,Leiomyoma Cutis,Retinal Hemangioblastoma,Pheochromocytoma,Hypoxia,Von Hippel-Lindau Syndrome,Renal Cell Carcinoma, Nonpapillary,Cardiovascular Organ Benign Neoplasm,Erythrocytosis, Familial, 2 |
5n4w_a | Q13617 | ENSG00000108094 | CUL2 | 100.00 | 5.40E-38 | 6.00E-42 | 354.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |