| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YNL049C | SFB2 | SGDID:S000004994 | Caci_2163 |
Caci_2163 |
Catenulispora acidiphila | 4fx5_a | C7QHQ7 | 99.70 | 5.80E-23 | 4.20E-27 | 231.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YNL049C | SFB2 | SGDID:S000004994 | Saci_1209 |
Saci_1209 |
Sulfolobus acidocaldarius | 5a8j_a | Q4J9H5 | 99.70 | 2.60E-21 | 1.90E-25 | 211.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YNL049C | SFB2 | SGDID:S000004994 | SEC24C KIAA0079 |
Protein transport protein Sec24C (SEC24-related protein C) |
Homo sapiens | Cataract 34, Multiple Types,Anemia, Congenital Dyserythropoietic, Type Ii,Digeorge Syndrome,Craniolenticulosutural Dysplasia,Ceroid Lipofuscinosis, Neuronal, 8 |
3eh2_a | P53992 | ENSG00000176986 | SEC24C | 100.00 | 7.80E-93 | 5.60E-97 | 859.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL049C | SFB2 | SGDID:S000004994 | SEC23 YPR181C P9705.14 |
Protein transport protein SEC23 |
Saccharomyces cerevisiae | 1m2o_a | P15303 | 100.00 | 5.50E-83 | 4.00E-87 | 773.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YNL049C | SFB2 | SGDID:S000004994 | SEC24D KIAA0755 |
Protein transport protein Sec24D (SEC24-related protein D) |
Homo sapiens | Carpenter Syndrome 2,Anemia, Congenital Dyserythropoietic, Type Ii,Disease Of Mental Health,Brittle Bone Disorder,Odontochondrodysplasia,Cole-Carpenter Syndrome 2,Craniolenticulosutural Dysplasia,Cole-Carpenter Syndrome |
3efo_b | O94855 | ENSG00000150961 | SEC24D | 100.00 | 2.40E-93 | 1.70E-97 | 864.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL049C | SFB2 | SGDID:S000004994 | SEC23A |
Protein transport protein Sec23A (hSec23A) (SEC23-related protein A) |
Homo sapiens | Camptodactyly-Tall Stature-Scoliosis-Hearing Loss Syndrome,Noonan Syndrome 1,Congenital Dyserythropoietic Anemia,Anemia, Congenital Dyserythropoietic, Type Ii,Photoallergic Dermatitis,Spondyloepiphyseal Dysplasia Congenita,Craniolenticulosutural Dysplasia,Cole-Carpenter Syndrome |
2nut_a | Q15436 | ENSG00000100934 | SEC23A | 100.00 | 2.90E-81 | 2.10E-85 | 758.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YNL049C | SFB2 | SGDID:S000004994 | SEC24 ANU1 YIL109C |
Protein transport protein SEC24 (Abnormal nuclear morphology 1) |
Saccharomyces cerevisiae | 1pcx_a | P40482 | 100.00 | 1.00E-106 | 1.00E-110 | 978.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YNL049C | SFB2 | SGDID:S000004994 | SEC24B |
Protein transport protein Sec24B (SEC24-related protein B) |
Homo sapiens | Myasthenic Syndrome, Congenital, 4c, Associated With Acetylcholine Receptor Deficiency,Anemia, Congenital Dyserythropoietic, Type Ii,Vas Deferens, Congenital Bilateral Aplasia Of,Brittle Bone Disorder,Neural Tube Defects,Chylomicron Retention Disease,Craniolenticulosutural Dysplasia,Hyperekplexia |
3eh1_a | O95487 | ENSG00000138802 | SEC24B | 100.00 | 3.50E-92 | 2.50E-96 | 851.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |