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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YLR293C | GSP1 | SGDID:S000004284 | GSP1 CNR1 CST17 YLR293C L8003.19 |
GTP-binding nuclear protein GSP1/CNR1 (Chromosome stability protein 17) (GTPase Ran homolog) (Genetic suppressor of PRP20-1) |
Saccharomyces cerevisiae | 2x19_a | P32835 | 99.90 | 5.80E-31 | 9.10E-35 | 175.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLR293C | GSP1 | SGDID:S000004284 | YPT31 CAALFM_CR07520CA orf19.2622 |
YPT31 CAALFM_CR07520CA orf19.2622 |
Candida albicans | 5ub8_a | A0A1D8PTI2 | 99.80 | 1.20E-24 | 1.70E-28 | 156.60 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLR293C | GSP1 | SGDID:S000004284 | GSP1 ECU04_1560 |
GTP-binding nuclear protein GSP1 (GTPase Ran homolog) |
Encephalitozoon cuniculi | 4djt_a | Q8SS11 | 99.90 | 5.20E-29 | 7.40E-33 | 180.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLR293C | GSP1 | SGDID:S000004284 | RAB8A MEL RAB8 |
Ras-related protein Rab-8A (Oncogene c-mel) |
Homo sapiens | Retinitis Pigmentosa,Sphingolipidosis,Bardet-Biedl Syndrome,Primary Ciliary Dyskinesia,Legionnaire Disease,Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1,Joubert Syndrome 3,Nephronophthisis,Leber Plus Disease,Retinal Degeneration,Fundus Dystrophy,Parkinson Disease, Late-Onset,Open-Angle Glaucoma,Cone-Rod Dystrophy 2,Bardet-Biedl Syndrome 6,Bardet-Biedl Syndrome 8,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Fanconi Renotubular Syndrome 1,Asphyxiating Thoracic Dystrophy,Glaucoma, Primary Open Angle,Glaucoma, Normal Tension,Meckel Syndrome, Type 1,Carpenter Syndrome 1,Lowe Oculocerebrorenal Syndrome,Diarrhea 2, With Microvillus Atrophy,Autosomal Recessive Non-Syndromic Intellectual Disability,Congenital Diarrhea,Griscelli Syndrome,Bardet-Biedl Syndrome 3,Martsolf Syndrome,Joubert Syndrome 1,Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease |
4lhw_c | P61006 | ENSG00000167461 | RAB8A | 99.80 | 1.10E-23 | 1.70E-27 | 139.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YLR293C | GSP1 | SGDID:S000004284 | RAB9A RAB9 |
Ras-related protein Rab-9A |
Canis lupus | 1s8f_b | P24408 | 99.80 | 2.30E-24 | 3.70E-28 | 143.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YLR293C | GSP1 | SGDID:S000004284 | RAP1A KREV1 |
Ras-related protein Rap-1A (EC 3.6.5.2) (C21KG) (G-22K) (GTP-binding protein smg p21A) (Ras-related protein Krev-1) |
3.6.5.2 | Homo sapiens | Bone Epithelioid Hemangioma,Leukocyte Adhesion Deficiency, Type Iii,Babesiosis,Cervical Non-Keratinizing Squamous Cell Carcinoma,Glanzmann Thrombasthenia,Osteoporosis,Tuberous Sclerosis,Breast Cancer,Meier-Gorlin Syndrome 1,Cerebral Cavernous Malformations,Leukocyte Adhesion Deficiency, Type I,Chronic Granulomatous Disease,Bleeding Disorder, Platelet-Type, 18,Klippel-Trenaunay-Weber Syndrome |
1c1y_a | P62834 | 99.90 | 1.70E-31 | 2.30E-35 | 192.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
YLR293C | GSP1 | SGDID:S000004284 | RAN ARA24 OK/SW-cl.81 |
GTP-binding nuclear protein Ran (Androgen receptor-associated protein 24) (GTPase Ran) (Ras-like protein TC4) (Ras-related nuclear protein) |
Homo sapiens | Teratocarcinoma,Hutchinson-Gilford Progeria Syndrome,Fragile X Tremor/Ataxia Syndrome,Spondylolisthesis,Vici Syndrome,X-Linked Chondrodysplasia Punctata 1,Pelizaeus-Merzbacher Disease |
1rrp_a | P62826 | ENSG00000132341 | RAN | 99.90 | 8.80E-33 | 1.40E-36 | 189.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |