| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YMR201C | RAD14 | SGDID:S000004814 | XPA XPAC |
DNA repair protein complementing XP-A cells (Xeroderma pigmentosum group A-complementing protein) |
Homo sapiens | Gastroesophageal Adenocarcinoma,Robinow Syndrome, Autosomal Recessive 1,Cockayne Syndrome A,Brain Sarcoma,Ocular Cancer,Xeroderma Pigmentosum Group E,Basal Cell Carcinoma,Laminopathy,Basal Cell Nevus Syndrome,Conjunctival Degeneration,Cockayne Syndrome,Ovarian Cancer,Trichothiodystrophy,Skin Benign Neoplasm,Xeroderma Pigmentosum, Complementation Group A,Xeroderma Pigmentosum, Complementation Group C,Xeroderma Pigmentosum, Complementation Group D,Xeroderma Pigmentosum, Complementation Group E,Fanconi Anemia, Complementation Group C,Xeroderma Pigmentosum, Variant Type,Fanconi Anemia, Complementation Group A,Xeroderma Pigmentosum, Complementation Group F,Xeroderma Pigmentosum, Complementation Group G,Skin Carcinoma,Hutchinson-Gilford Progeria Syndrome,Mutagen Sensitivity,Xeroderma Pigmentosum, Complementation Group B,Xfe Progeroid Syndrome,Photoparoxysmal Response 1,Multiple Self-Healing Squamous Epithelioma,Autosomal Recessive Disease,Autosomal Genetic Disease,Uv-Sensitive Syndrome,Ataxia-Telangiectasia,Lung Cancer |
1d4u_a | P23025 | ENSG00000136936 | XPA | 99.60 | 1.20E-20 | 1.20E-24 | 149.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YMR201C | RAD14 | SGDID:S000004814 | RAD14 YMR201C YM8325.02C |
DNA repair protein RAD14 |
Saccharomyces cerevisiae | 5a39_b | P28519 | 99.80 | 5.00E-24 | 5.00E-28 | 173.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YMR201C | RAD14 | SGDID:S000004814 | SLC30A9 C4orf1 HUEL |
Zinc transporter 9 (ZnT-9) (Human embryonic lung protein) (HuEL) (Solute carrier family 30 member 9) |
Homo sapiens | Hypermanganesemia With Dystonia,Birk-Landau-Perez Syndrome,Hemochromatosis, Type 5,Hemochromatosis, Type 1,Hypermanganesemia With Dystonia 2 |
2enk_a | Q6PML9 | ENSG00000014824 | SLC30A9 | 99.40 | 6.20E-18 | 5.70E-22 | 136.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |