| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YGL095C | VPS45 | SGDID:S000003063 | Sec1-like protein |
Sec1-like protein |
Doryteuthis pealeii | 1fvh_a | O62547 | 100.00 | 1.60E-73 | 1.10E-77 | 614.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YGL095C | VPS45 | SGDID:S000003063 | VPS33A |
Vacuolar protein sorting-associated protein 33A (hVPS33A) |
Homo sapiens | Mucopolysaccharidosis-Plus Syndrome,Lysosomal Disease,Vulto-Van Silfhout-De Vries Syndrome,Hermansky-Pudlak Syndrome |
4bx8_a | Q96AX1 | ENSG00000139719 | VPS33A | 100.00 | 2.80E-70 | 1.90E-74 | 590.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YGL095C | VPS45 | SGDID:S000003063 | Stxbp1 Unc18a |
Syntaxin-binding protein 1 (N-Sec1) (Protein unc-18 homolog 1) (Unc18-1) (Protein unc-18 homolog A) (Unc-18A) (p67) (rbSec1) |
Rattus norvegicus | 4jeh_a | P61765 | 100.00 | 6.10E-72 | 4.20E-76 | 602.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YGL095C | VPS45 | SGDID:S000003063 | 32602 |
32602 |
Monosiga brevicollis | 2xhe_a | A9V0L3 | 100.00 | 8.50E-71 | 5.80E-75 | 597.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YGL095C | VPS45 | SGDID:S000003063 | STXBP2 UNC18B |
Syntaxin-binding protein 2 (Protein unc-18 homolog 2) (Unc18-2) (Protein unc-18 homolog B) (Unc-18B) |
Homo sapiens | Selective Immunoglobulin Deficiency Disease,Chediak-Higashi Syndrome,Hemophagocytic Lymphohistiocytosis, Familial, 1,Dysgammaglobulinemia,Pancytopenia,Lymphoproliferative Syndrome 1,Lymphoproliferative Syndrome 2,Hemophagocytic Lymphohistiocytosis, Familial, 5,Acute Hemorrhagic Encephalitis,Trichohepatoenteric Syndrome 1,Piebald Trait,Hemophagocytic Lymphohistiocytosis, Familial, 4,Hemophagocytic Lymphohistiocytosis, Familial, 2,Thrombocytopenia,Hermansky-Pudlak Syndrome,Hemophagocytic Lymphohistiocytosis,Osmotic Diarrhea,Lymphoproliferative Syndrome, X-Linked, 2,Lymphoproliferative Syndrome, X-Linked, 1,Griscelli Syndrome, Type 2,Diarrhea 2, With Microvillus Atrophy,Congenital Diarrhea,Griscelli Syndrome |
4cca_a | Q15833 | ENSG00000076944 | STXBP2 | 100.00 | 1.60E-71 | 1.10E-75 | 598.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |