| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YDR425W | SNX41 | SGDID:S000002833 | SNX9 SH3PX1 SH3PXD3A |
Sorting nexin-9 (SH3 and PX domain-containing protein 1) (Protein SDP1) (SH3 and PX domain-containing protein 3A) |
Homo sapiens | Cataract 8, Multiple Types,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Wiskott-Aldrich Syndrome,Autosomal Dominant Non-Syndromic Intellectual Disability |
3dyt_a | Q9Y5X1 | ENSG00000130340 | SNX9 | 99.00 | 4.90E-14 | 6.20E-18 | 131.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR425W | SNX41 | SGDID:S000002833 | SNX16 |
Sorting nexin-16 |
Homo sapiens | Spinocerebellar Ataxia 15 |
5gw0_c | P57768 | ENSG00000104497 | SNX16 | 98.80 | 6.20E-13 | 7.50E-17 | 113.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR425W | SNX41 | SGDID:S000002833 | SNX11 |
Sorting nexin-11 |
Homo sapiens | Coffin-Siris Syndrome 1 |
4ikb_a | Q9Y5W9 | ENSG00000002919 | SNX11 | 98.70 | 1.20E-12 | 1.50E-16 | 108.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR425W | SNX41 | SGDID:S000002833 | snx25 |
snx25 |
Danio rerio | 5xdz_b | C6K2H9 | 98.90 | 2.70E-13 | 3.50E-17 | 105.70 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | ||||
| YDR425W | SNX41 | SGDID:S000002833 | SNX7 |
Sorting nexin-7 |
Homo sapiens | Hereditary Spastic Paraplegia,Spastic Paraplegia 29, Autosomal Dominant |
3iq2_b | Q9UNH6 | ENSG00000162627 | SNX7 | 98.80 | 8.90E-13 | 1.10E-16 | 106.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR425W | SNX41 | SGDID:S000002833 | 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 | 98.90 | 2.00E-13 | 2.70E-17 | 105.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YDR425W | SNX41 | SGDID:S000002833 | SNX17 KIAA0064 |
Sorting nexin-17 |
Homo sapiens | Retinitis Pigmentosa |
3lui_b | Q15036 | ENSG00000115234 | SNX17 | 98.80 | 5.30E-13 | 6.90E-17 | 103.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR425W | SNX41 | SGDID:S000002833 | 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 | 98.90 | 1.10E-13 | 1.20E-17 | 124.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR425W | SNX41 | SGDID:S000002833 | CTHT_0068290 |
CTHT_0068290 |
Chaetomium thermophilum | 6h7w_l | G0SH11 | 98.90 | 2.70E-13 | 3.40E-17 | 107.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YDR425W | SNX41 | SGDID:S000002833 | 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 |
4pqo_a | Q9Y5W7 | ENSG00000135317 | SNX14 | 98.80 | 8.10E-13 | 1.00E-16 | 105.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR425W | SNX41 | SGDID:S000002833 | 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 | 99.10 | 7.50E-15 | 7.90E-19 | 127.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YDR425W | SNX41 | SGDID:S000002833 | SNX27 KIAA0488 My014 |
Sorting nexin-27 |
Homo sapiens | Epilepsy,Parkinson Disease, Late-Onset,Dravet Syndrome,Chromosomal Duplication Syndrome |
4has_b | Q96L92 | ENSG00000143376 | SNX27 | 98.90 | 2.50E-13 | 3.10E-17 | 111.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YDR425W | SNX41 | SGDID:S000002833 | SNX33 SH3PX3 SH3PXD3C SNX30 |
Sorting nexin-33 (SH3 and PX domain-containing protein 3) |
Homo sapiens | D-2-Hydroxyglutaric Aciduria 1 |
4akv_b | Q8WV41 | ENSG00000173548 | SNX33 | 99.10 | 5.90E-15 | 7.20E-19 | 140.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |