| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YHR105W | YPT35 | SGDID:S000001147 | SNX3 GRD19 YOR357C |
Sorting nexin-3 (Golgi retention deficient protein 19) |
Saccharomyces cerevisiae | 1ocu_a | Q08826 | 99.00 | 2.70E-14 | 2.20E-18 | 107.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YHR105W | YPT35 | SGDID:S000001147 | SNX11 |
Sorting nexin-11 |
Homo sapiens | Coffin-Siris Syndrome 1 |
4ikb_a | Q9Y5W9 | ENSG00000002919 | SNX11 | 99.10 | 1.60E-14 | 1.30E-18 | 106.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR105W | YPT35 | SGDID:S000001147 | NCF1 NOXO2 SH3PXD1A |
Neutrophil cytosol factor 1 (NCF-1) (47 kDa autosomal chronic granulomatous disease protein) (47 kDa neutrophil oxidase factor) (NCF-47K) (Neutrophil NADPH oxidase factor 1) (Nox organizer 2) (Nox-organizing protein 2) (SH3 and PX domain-containing protein 1A) (p47-phox) |
Homo sapiens | Ectodermal Dysplasia,Suppurative Lymphadenitis,Cardiomyopathy, Familial Hypertrophic, 4,Phagocyte Bactericidal Dysfunction,Chronic Granulomatous Disease,Retinitis Pigmentosa 47,Granulomatous Disease, Chronic, Autosomal Recessive, 4,Granulomatous Disease, Chronic, Autosomal Recessive, 1,Granulomatous Disease, Chronic, Autosomal Recessive, 3,Hypertension, Essential,Granulomatous Disease, Chronic, X-Linked,Lung Abscess |
1gd5_a | P14598 | ENSG00000158517 | NCF1 | 98.90 | 1.40E-13 | 1.10E-17 | 99.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR105W | YPT35 | SGDID:S000001147 | SNX7 |
Sorting nexin-7 |
Homo sapiens | Hereditary Spastic Paraplegia,Spastic Paraplegia 29, Autosomal Dominant |
3iq2_b | Q9UNH6 | ENSG00000162627 | SNX7 | 99.00 | 5.80E-14 | 4.70E-18 | 102.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR105W | YPT35 | SGDID:S000001147 | CTHT_0068290 |
CTHT_0068290 |
Chaetomium thermophilum | 6h7w_l | G0SH11 | 99.10 | 2.30E-14 | 1.90E-18 | 103.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YHR105W | YPT35 | SGDID:S000001147 | SNX25 MSTP043 |
Sorting nexin-25 |
Homo sapiens | Facioscapulohumeral Muscular Dystrophy 1,Spinocerebellar Ataxia, Autosomal Recessive 20 |
5woe_a | Q9H3E2 | ENSG00000109762 | SNX25 | 99.00 | 8.80E-14 | 7.40E-18 | 98.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR105W | YPT35 | SGDID:S000001147 | NCF4 SH3PXD4 |
Neutrophil cytosol factor 4 (NCF-4) (Neutrophil NADPH oxidase factor 4) (SH3 and PX domain-containing protein 4) (p40-phox) (p40phox) |
Homo sapiens | Granular Corneal Dystrophy,Phagocyte Bactericidal Dysfunction,Chronic Granulomatous Disease,Anorectal Stricture,Granulomatous Disease, Chronic, Autosomal Recessive, 4,Granulomatous Disease, Chronic, Autosomal Recessive, 3,Granulomatous Disease, Chronic, X-Linked,Corneal Dystrophy, Avellino Type,Epithelial-Stromal Tgfbi Dystrophy |
1h6h_a | Q15080 | 99.50 | 2.30E-18 | 1.80E-22 | 129.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YHR105W | YPT35 | SGDID:S000001147 | SNX17 KIAA0064 |
Sorting nexin-17 |
Homo sapiens | Retinitis Pigmentosa |
3lui_b | Q15036 | ENSG00000115234 | SNX17 | 98.90 | 1.40E-13 | 1.20E-17 | 96.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR105W | YPT35 | SGDID:S000001147 | SNX10 |
Sorting nexin-10 |
Homo sapiens | Craniodiaphyseal Dysplasia,Osteopetrosis, Autosomal Recessive 8,Autosomal Recessive Malignant Osteopetrosis,Osteopetrosis,Craniometaphyseal Dysplasia, Autosomal Dominant,Osteopetrosis, Autosomal Recessive 3 |
4on3_a | Q9Y5X0 | ENSG00000086300 | SNX10 | 99.20 | 3.80E-15 | 3.00E-19 | 118.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR105W | YPT35 | SGDID:S000001147 | SNX16 |
Sorting nexin-16 |
Homo sapiens | Spinocerebellar Ataxia 15 |
5gw0_c | P57768 | ENSG00000104497 | SNX16 | 99.10 | 2.50E-14 | 2.00E-18 | 109.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR105W | YPT35 | SGDID:S000001147 | SNX14 |
Sorting nexin-14 |
Homo sapiens | Boucher-Neuhauser Syndrome,Cohen Syndrome,Neurodegeneration With Brain Iron Accumulation,Spinocerebellar Ataxia 20,Spastic Paraplegia 49, Autosomal Recessive,Cerebellar Disease,Spinocerebellar Ataxia 13,Neurodegeneration With Brain Iron Accumulation 5,Vici Syndrome,Alcohol-Related Neurodevelopmental Disorder,Spinocerebellar Ataxia, Autosomal Recessive 20,Mental Retardation, Autosomal Dominant 38,Autosomal Recessive Cerebellar Ataxia,Hereditary Ataxia,Autosomal Recessive Non-Syndromic Intellectual Disability |
4bgj_a | Q9Y5W7 | ENSG00000135317 | SNX14 | 99.00 | 3.90E-14 | 3.10E-18 | 105.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR105W | YPT35 | SGDID:S000001147 | PIK3C2G |
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma (PI3K-C2-gamma) (PtdIns-3-kinase C2 subunit gamma) (EC 2.7.1.154) (Phosphoinositide 3-kinase-C2-gamma) |
2.7.1.154 | Homo sapiens | Viral Labyrinthitis,Spermatogenic Failure 17 |
2wwe_a | O75747 | ENSG00000139144 | PIK3C2G | 98.90 | 1.40E-13 | 1.20E-17 | 99.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YHR105W | YPT35 | SGDID:S000001147 | SNX15 |
Sorting nexin-15 |
Homo sapiens | Hereditary Spastic Paraplegia |
6ecm_a | Q9NRS6 | ENSG00000110025 | SNX15 | 99.00 | 3.90E-14 | 3.20E-18 | 101.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YHR105W | YPT35 | SGDID:S000001147 | snx25 |
snx25 |
Danio rerio | 5xdz_b | C6K2H9 | 99.00 | 3.70E-14 | 3.10E-18 | 100.60 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | ||||
| YHR105W | YPT35 | SGDID:S000001147 | SGK3 CISK SGKL |
Serine/threonine-protein kinase Sgk3 (EC 2.7.11.1) (Cytokine-independent survival kinase) (Serum/glucocorticoid-regulated kinase 3) (Serum/glucocorticoid-regulated kinase-like) |
2.7.11.1 | Homo sapiens | Breast Cancer |
6edx_a | Q96BR1 | ENSG00000104205 | C8orf44-SGK3 | 99.00 | 2.70E-14 | 2.20E-18 | 100.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |