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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
YGL212W | VAM7 | SGDID:S000003180 | SEC9 HSS7 YGR009C |
Protein transport protein SEC9 |
Saccharomyces cerevisiae | 3b5n_d | P40357 | 98.50 | 4.50E-11 | 3.80E-15 | 83.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGL212W | VAM7 | SGDID:S000003180 | 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 | 98.50 | 1.70E-11 | 1.50E-15 | 112.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | Snx5 |
Sorting nexin-5 |
Rattus norvegicus | 3hpc_x | B1H267 | 98.70 | 4.90E-12 | 4.00E-16 | 105.30 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGL212W | VAM7 | SGDID:S000003180 | 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 | 98.50 | 2.00E-11 | 1.70E-15 | 113.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | botA bna CBO0806 CLC_0862 |
Botulinum neurotoxin type A (BoNT/A) (Bontoxilysin-A) (BOTOX) [Cleaved into: Botulinum neurotoxin A light chain (LC) (EC 3.4.24.69); Botulinum neurotoxin A heavy chain (HC)] |
3.4.24.69 | Clostridium botulinum | 3zus_d | P0DPI1 | ENSG00000092531 | SNAP23 | 98.80 | 1.80E-12 | 1.30E-16 | 131.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | SNX11 |
Sorting nexin-11 |
Homo sapiens | Coffin-Siris Syndrome 1 |
4ikb_a | Q9Y5W9 | ENSG00000002919 | SNX11 | 98.60 | 1.20E-11 | 1.00E-15 | 99.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | NOXO1 P41NOX SH3PXD5 |
NADPH oxidase organizer 1 (NADPH oxidase regulatory protein) (Nox organizer 1) (Nox-organizing protein 1) (SH3 and PX domain-containing protein 5) |
Homo sapiens | Phagocyte Bactericidal Dysfunction,Lung Mucoepidermoid Carcinoma |
2l73_a | Q8NFA2 | ENSG00000196408 | NOXO1 | 98.50 | 3.90E-11 | 3.40E-15 | 96.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | 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 | 98.60 | 5.90E-12 | 5.20E-16 | 98.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YGL212W | VAM7 | SGDID:S000003180 | SNX7 |
Sorting nexin-7 |
Homo sapiens | Hereditary Spastic Paraplegia,Spastic Paraplegia 29, Autosomal Dominant |
3iq2_b | Q9UNH6 | ENSG00000162627 | SNX7 | 98.70 | 4.90E-12 | 4.30E-16 | 100.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | SNX3 GRD19 YOR357C |
Sorting nexin-3 (Golgi retention deficient protein 19) |
Saccharomyces cerevisiae | 1ocu_a | Q08826 | 98.50 | 2.40E-11 | 2.10E-15 | 99.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGL212W | VAM7 | SGDID:S000003180 | PIK3C2A |
Phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit alpha (PI3K-C2-alpha) (PtdIns-3-kinase C2 subunit alpha) (EC 2.7.1.137) (EC 2.7.1.153) (EC 2.7.1.154) (Phosphoinositide 3-kinase-C2-alpha) |
2.7.1.154 | Homo sapiens | Muscular Disease,Pulmonary Edema,Heart Disease,Cardiac Tamponade,Mitral Valve Insufficiency,Myoglobinuria,Mutism,Myopathy,Calcinosis,Gas Gangrene,Coronary Stenosis,Familial Hyperlipidemia,Speech Disorder,Acne,Diabetes Mellitus,Pericardial Effusion,Muscle Tissue Disease,Status Asthmaticus,Orbital Plasma Cell Granuloma,Coronary Artery Vasospasm,Acute Myocardial Infarction,Bacterial Meningitis,Hypertrophic Cardiomyopathy,Compartment Syndrome,Sarcoid Meningitis,Myocardial Infarction,Polymyositis,Lung Mixed Small Cell And Squamous Cell Carcinoma,Sarcocystosis,Myositis,Legionnaire Disease,Apparent Mineralocorticoid Excess,Dengue Disease,Toxic Myocarditis,Hemorrhagic Disease,Crimean-Congo Hemorrhagic Fever,Trichinosis,Leptospirosis,Muscular Dystrophy,Trichostrongylosis,Acute Kidney Tubular Necrosis,Chronic Progressive External Ophthalmoplegia,Isolated Elevated Serum Creatine Phosphokinase Levels,Interstitial Myocarditis,Myocarditis,Barbiturate Dependence,Quadriplegia,Scleromyxedema,Pleural Lipoma,Dermatomyositis,Autoimmune Hypoparathyroidism,Malignant Hyperthermia,Left Bundle Branch Hemiblock,Heart Conduction Disease,Endocarditis,Pneumonia,Perinephritis,Anuria,Pyomyositis,Acute Kidney Failure,Intermediate Coronary Syndrome,Vibrio Vulnificus Infection,Patent Foramen Ovale,Virus Associated Hemophagocytic Syndrome,Acute Mountain Sickness,Acute Anterolateral Myocardial Infarction,Myringitis Bullosa Hemorrhagica,Rectum Neuroendocrine Neoplasm,Posteroinferior Myocardial Infarction,Posterior Myocardial Infarction,Subendocardial Myocardial Infarction,Inferior Myocardial Infarction,Lateral Myocardial Infarction,Chronic Orbital Inflammation,Anteroseptal Myocardial Infarction,Epidemic Pleurodynia,Congestive Heart Failure,Dysphagia,Angina Pectoris,Childhood Type Dermatomyositis,Ischemia,Neuroleptic Malignant Syndrome,Respiratory Failure,Hypothyroidism,Granulomatous Myositis,Disseminated Intravascular Coagulation,Ornithosis,Erysipelas,Disease Of Mental Health,Thrombocytopenia,Muscular Dystrophy, Becker Type,Glycogen Storage Disease Iii,Type 2 Diabetes Mellitus,Co-Trimoxazole Allergy,Aspiration Pneumonia,Extrinsic Cardiomyopathy,Basidiobolomycosis,Exanthem,Spondylolisthesis,Strabismus,Oculoskeletodental Syndrome,Diabetes Mellitus, Ketosis-Prone,Atrioventricular Block,Endocardium Disease,Pericardium Disease,Hypertension, Essential,Lipoprotein Quantitative Trait Locus,Muscular Dystrophy, Duchenne Type,Cardiac Arrest,Ectopic Pregnancy,Myxedema,Miyoshi Muscular Dystrophy,Polycystic Kidney Disease 4 With Or Without Polycystic Liver Disease |
2ar5_a | O00443 | ENSG00000011405 | PIK3C2A | 98.40 | 4.90E-11 | 4.40E-15 | 91.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YGL212W | VAM7 | SGDID:S000003180 | SNX25 MSTP043 |
Sorting nexin-25 |
Homo sapiens | Facioscapulohumeral Muscular Dystrophy 1,Spinocerebellar Ataxia, Autosomal Recessive 20 |
5woe_a | Q9H3E2 | ENSG00000109762 | SNX25 | 98.50 | 3.70E-11 | 3.40E-15 | 92.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | SNX16 |
Sorting nexin-16 |
Homo sapiens | Spinocerebellar Ataxia 15 |
5gw0_c | P57768 | ENSG00000104497 | SNX16 | 98.70 | 3.90E-12 | 3.40E-16 | 105.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | Stx8 |
Syntaxin-8 |
Rattus norvegicus | 1gl2_d | Q9Z2Q7 | 98.50 | 4.40E-11 | 3.70E-15 | 84.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGL212W | VAM7 | SGDID:S000003180 | snx25 |
snx25 |
Danio rerio | 5xdz_b | C6K2H9 | 98.70 | 3.90E-12 | 3.50E-16 | 97.60 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | ||||
YGL212W | VAM7 | SGDID:S000003180 | 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 | 98.70 | 5.10E-12 | 4.60E-16 | 96.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |
YGL212W | VAM7 | SGDID:S000003180 | 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 | 98.60 | 6.80E-12 | 6.10E-16 | 97.80 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | 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 | 98.80 | 8.40E-13 | 7.10E-17 | 114.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | Synaptosomal-associated protein |
Synaptosomal-associated protein |
Doryteuthis pealeii | 1l4a_d | Q8T3S4 | 98.50 | 3.20E-11 | 2.60E-15 | 90.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGL212W | VAM7 | SGDID:S000003180 | SNAP29 |
Synaptosomal-associated protein 29 (SNAP-29) (Soluble 29 kDa NSF attachment protein) (Vesicle-membrane fusion protein SNAP-29) |
Homo sapiens | Ichthyosis,Pelizaeus-Merzbacher-Like Disease,Leukodystrophy, Hypomyelinating, 2,Neuropathy,Leukodystrophy,Mental Retardation, Enteropathy, Deafness, Peripheral Neuropathy, Ichthyosis, And Keratoderma,Cerebral Dysgenesis, Neuropathy, Ichthyosis, And Palmoplantar Keratoderma Syndrome,Bernard-Soulier Syndrome,Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive,Erythrokeratodermia Variabilis Et Progressiva 1,T-Cell Immunodeficiency With Thymic Aplasia,Vici Syndrome,Tetralogy Of Fallot,Digeorge Syndrome,Opitz-Gbbb Syndrome,Velocardiofacial Syndrome,Van Den Ende-Gupta Syndrome |
4wy4_d | O95721 | 98.40 | 5.20E-11 | 4.30E-15 | 83.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |||
YGL212W | VAM7 | SGDID:S000003180 | 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 | 98.60 | 1.60E-11 | 1.40E-15 | 98.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | SNX17 KIAA0064 |
Sorting nexin-17 |
Homo sapiens | Retinitis Pigmentosa |
3lui_b | Q15036 | ENSG00000115234 | SNX17 | 98.60 | 6.80E-12 | 6.20E-16 | 95.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | STX6 |
Syntaxin-6 |
Homo sapiens | Supranuclear Palsy, Progressive, 1,Leukodystrophy, Hypomyelinating, 6 |
2nps_d | O43752 | ENSG00000135823 | STX6 | 98.50 | 2.00E-11 | 1.60E-15 | 90.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | SNX15 |
Sorting nexin-15 |
Homo sapiens | Hereditary Spastic Paraplegia |
6ecm_a | Q9NRS6 | ENSG00000110025 | SNX15 | 98.70 | 3.80E-12 | 3.40E-16 | 99.10 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YGL212W | VAM7 | SGDID:S000003180 | Snap25 Snap |
Synaptosomal-associated protein 25 (SNAP-25) (Super protein) (SUP) (Synaptosomal-associated 25 kDa protein) |
Rattus norvegicus | 1n7s_d | P60881 | 98.50 | 2.80E-11 | 2.30E-15 | 85.20 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGL212W | VAM7 | SGDID:S000003180 | CTHT_0068290 |
CTHT_0068290 |
Chaetomium thermophilum | 6h7w_l | G0SH11 | 98.70 | 1.90E-12 | 1.70E-16 | 100.90 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YGL212W | VAM7 | SGDID:S000003180 | SNX27 KIAA0488 My014 |
Sorting nexin-27 |
Homo sapiens | Epilepsy,Parkinson Disease, Late-Onset,Dravet Syndrome,Chromosomal Duplication Syndrome |
4has_b | Q96L92 | ENSG00000143376 | SNX27 | 98.50 | 3.40E-11 | 2.90E-15 | 95.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |