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AnalogYeast
One stop shop for finding analogs for your favorite yeast protein

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YGL212W VAM7 / SGDID:S000003180
SGD CSV
Disease Associated
Homo Sapiens
Mus Musculus
Danio Rerio
Drosophila Melanogaster
Caenorhabditis Elegans
Arabidopsis Thaliana
Escherichia Coli
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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
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

Weizmann Institute of Science | Maya Schuldiner Lab