| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YJL049W | YJL049W | SGDID:S000003585 | VPS25 DERP9 EAP20 |
Vacuolar protein-sorting-associated protein 25 (hVps25) (Dermal papilla-derived protein 9) (ELL-associated protein of 20 kDa) (ESCRT-II complex subunit VPS25) |
Homo sapiens | Rigid Spine Muscular Dystrophy 1,Cone-Rod Dystrophy 2,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7 |
3cuq_c | Q9BRG1 | ENSG00000131475 | VPS25 | 99.90 | 2.60E-30 | 2.00E-34 | 230.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL049W | YJL049W | SGDID:S000003585 | VPS25 VPT25 YJR102C J1957 |
Vacuolar protein-sorting-associated protein 25 (ESCRT-II complex subunit VPS25) |
Saccharomyces cerevisiae | 1w7p_b | P47142 | 99.90 | 6.90E-30 | 5.20E-34 | 232.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YJL049W | YJL049W | SGDID:S000003585 | CHMP3 CGI149 NEDF VPS24 CGI-149 |
Charged multivesicular body protein 3 (Chromatin-modifying protein 3) (Neuroendocrine differentiation factor) (Vacuolar protein sorting-associated protein 24) (hVps24) |
Homo sapiens | Nemaline Myopathy 1,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 7 |
2gd5_d | Q9Y3E7 | ENSG00000249884 | RNF103-CHMP3 | 99.60 | 2.00E-19 | 1.50E-23 | 159.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL049W | YJL049W | SGDID:S000003585 | CHMP1B C18orf2 |
Charged multivesicular body protein 1b (CHMP1.5) (Chromatin-modifying protein 1b) (CHMP1b) (Vacuolar protein sorting-associated protein 46-2) (Vps46-2) (hVps46-2) |
Homo sapiens | Spinal Cord Neuroblastoma,Spinal Cord Primitive Neuroectodermal Neoplasm,Pontocerebellar Hypoplasia, Type 8,Hereditary Spastic Paraplegia,Spastic Paraplegia 4, Autosomal Dominant,Pontocerebellar Hypoplasia, Type 1a |
6e8g_qb | Q7LBR1 | ENSG00000255112 | CHMP1B | 99.80 | 3.80E-24 | 2.90E-28 | 193.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YJL049W | YJL049W | SGDID:S000003585 | Snf7 |
Snf7 |
pfam Family | PF03357 | 99.50 | 1.20E-18 | 9.00E-23 | 155.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 |