| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| YOR357C | SNX3 | SGDID:S000005884 | 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 | 99.70 | 5.60E-22 | 3.60E-26 | 125.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
| YOR357C | SNX3 | SGDID:S000005884 | snx25 |
snx25 |
Danio rerio | 5xdz_b | C6K2H9 | 99.40 | 7.20E-17 | 4.70E-21 | 98.20 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | ||||
| YOR357C | SNX3 | SGDID:S000005884 | CTHT_0068290 |
CTHT_0068290 |
Chaetomium thermophilum | 6h7w_l | G0SH11 | 99.50 | 3.30E-18 | 2.20E-22 | 105.50 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YOR357C | SNX3 | SGDID:S000005884 | SNX3 |
Sorting nexin-3 (Protein SDP3) |
Homo sapiens | Syndromic Microphthalmia,Microphthalmia, Syndromic 8,Microphthalmia,Parkinson Disease, Late-Onset,Microcephaly,Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 |
2mxc_a | O60493 | ENSG00000112335 | SNX3 | 99.60 | 1.60E-19 | 1.00E-23 | 117.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOR357C | SNX3 | SGDID:S000005884 | 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 | 99.40 | 7.50E-18 | 4.90E-22 | 103.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YOR357C | SNX3 | SGDID:S000005884 | SNX16 |
Sorting nexin-16 |
Homo sapiens | Spinocerebellar Ataxia 15 |
5gw0_c | P57768 | ENSG00000104497 | SNX16 | 99.40 | 1.70E-17 | 1.10E-21 | 108.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOR357C | SNX3 | SGDID:S000005884 | SNX3 GRD19 YOR357C |
Sorting nexin-3 (Golgi retention deficient protein 19) |
Saccharomyces cerevisiae | 1ocu_a | Q08826 | 99.90 | 2.80E-27 | 1.90E-31 | 152.80 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
| YOR357C | SNX3 | SGDID:S000005884 | 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 | 99.40 | 2.60E-17 | 1.70E-21 | 99.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
| YOR357C | SNX3 | SGDID:S000005884 | SNX27 KIAA0488 My014 |
Sorting nexin-27 |
Homo sapiens | Epilepsy,Parkinson Disease, Late-Onset,Dravet Syndrome,Chromosomal Duplication Syndrome |
4has_b | Q96L92 | ENSG00000143376 | SNX27 | 99.40 | 7.30E-17 | 4.70E-21 | 100.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOR357C | SNX3 | SGDID:S000005884 | SNX15 |
Sorting nexin-15 |
Homo sapiens | Hereditary Spastic Paraplegia |
6ecm_a | Q9NRS6 | ENSG00000110025 | SNX15 | 99.40 | 3.20E-17 | 2.10E-21 | 100.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOR357C | SNX3 | SGDID:S000005884 | SNX12 |
Sorting nexin-12 |
Homo sapiens | 2csk_a | Q9UMY4 | ENSG00000147164 | SNX12 | 99.40 | 7.10E-17 | 4.60E-21 | 101.50 | 0 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | ||
| YOR357C | SNX3 | SGDID:S000005884 | SNX7 |
Sorting nexin-7 |
Homo sapiens | Hereditary Spastic Paraplegia,Spastic Paraplegia 29, Autosomal Dominant |
3iq2_b | Q9UNH6 | ENSG00000162627 | SNX7 | 99.40 | 1.10E-17 | 6.90E-22 | 104.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOR357C | SNX3 | SGDID:S000005884 | SNX11 |
Sorting nexin-11 |
Homo sapiens | Coffin-Siris Syndrome 1 |
4ikb_a | Q9Y5W9 | ENSG00000002919 | SNX11 | 99.40 | 7.50E-18 | 4.90E-22 | 106.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
| YOR357C | SNX3 | SGDID:S000005884 | 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 | 99.60 | 1.20E-19 | 8.00E-24 | 121.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |