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 |
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YDL035C | GPR1 | SGDID:S000002193 | CNR1 CNR |
Cannabinoid receptor 1 (CB-R) (CB1) (CANN6) |
Homo sapiens | Agnosia,Migraine With Or Without Aura 1,Bone Cancer,Cannabis Dependence,Diabetes Mellitus,Cerebral Angioma,Alcohol Dependence,Cannabis Abuse,Post-Traumatic Stress Disorder,Chromophobe Renal Cell Carcinoma,Constipation,Myocardial Infarction,Amyotrophic Lateral Sclerosis 1,Paroxysmal Dyskinesia,Doxorubicin Induced Cardiomyopathy,Paranoid Schizophrenia,Uremic Pruritus,Substance Dependence,Drug Dependence,Cocaine Dependence,Hallucinogen Dependence,Psychotic Disorder,Schizoaffective Disorder,Osteoporosis,Eating Disorder,Substance Abuse,Parkinson Disease, Late-Onset,Lipid Metabolism Disorder,Autoimmune Encephalitis,Chronic Pain,Central Nervous System Disease,Bipolar Disorder,Mood Disorder,Tendinosis,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Type 2 Diabetes Mellitus,Multiple Sclerosis,Schizophrenia,Asperger Syndrome,Intraocular Pressure Quantitative Trait Locus,Fetal Alcohol Spectrum Disorder,Early Infantile Epileptic Encephalopathy,Gilles De La Tourette Syndrome,Polysubstance Abuse,Anorexia Nervosa,Huntington Disease,Withdrawal Disorder,Autism Spectrum Disorder,Dravet Syndrome,Pain Agnosia,Anxiety,Autism,Cyclic Vomiting Syndrome |
5tgz_a | P21554 | ENSG00000118432 | CNR1 | 99.60 | 4.70E-20 | 5.70E-24 | 191.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | F2RL1 GPR11 PAR2 |
Proteinase-activated receptor 2 (PAR-2) (Coagulation factor II receptor-like 1) (G-protein coupled receptor 11) (Thrombin receptor-like 1) [Cleaved into: Proteinase-activated receptor 2, alternate cleaved 1; Proteinase-activated receptor 2, alternate cleaved 2] |
Homo sapiens | Rhinitis,Orofacial Granulomatosis,Pulmonary Vein Stenosis,Pancreatitis,Gastroesophageal Reflux,Granulomatous Orchitis,Papillary Adenocarcinoma,Dermatitis, Atopic,Neuroleptic Malignant Syndrome,Inflammatory Bowel Disease,Asthma,Pancreatic Cancer |
5nj6_a | P55085 | ENSG00000164251 | F2RL1 | 99.50 | 6.90E-19 | 8.60E-23 | 179.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | Chrm3 Chrm-3 |
Muscarinic acetylcholine receptor M3 |
Rattus norvegicus | 4u14_a | P08483 | 99.60 | 1.30E-19 | 1.50E-23 | 189.10 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL035C | GPR1 | SGDID:S000002193 | CNR2 CB2A CB2B |
Cannabinoid receptor 2 (CB-2) (CB2) (hCB2) (CX5) |
Homo sapiens | Polyarticular Juvenile Idiopathic Arthritis,Cannabis Abuse,Osteoporosis,Mood Disorder,Disease Of Mental Health,Body Mass Index Quantitative Trait Locus 11,Multiple Sclerosis,Chlorhexidine Allergy,Advanced Sleep Phase Syndrome, Familial, 3 |
5zty_a | P34972 | ENSG00000188822 | CNR2 | 99.50 | 4.60E-19 | 5.30E-23 | 190.90 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | Ocular_alb |
Ocular albinism type 1 protein |
pfam Family | PF02101 | 99.50 | 9.10E-19 | 1.10E-22 | 179.70 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | |||||
YDL035C | GPR1 | SGDID:S000002193 | HTR1B HTR1DB |
5-hydroxytryptamine receptor 1B (5-HT-1B) (5-HT1B) (S12) (Serotonin 1D beta receptor) (5-HT-1D-beta) (Serotonin receptor 1B) |
Homo sapiens | Narcolepsy,Migraine With Or Without Aura 1,Motion Sickness,Amphetamine Abuse,Alcohol Dependence,Major Depressive Disorder,Pyromania,Substance Dependence,Obsessive-Compulsive Disorder,Migraine With Aura,Psychosexual Disorder,Substance Abuse,Premature Ejaculation,Frontal Sinusitis,Panic Disorder,Angina Pectoris,Borderline Personality Disorder,Impulse Control Disorder,Antisocial Personality Disorder,Acute Frontal Sinusitis,Bipolar Disorder,Mood Disorder,Disease Of Mental Health,Personality Disorder,Pulmonary Hypertension,Alcohol Use Disorder,Mental Depression,Schizophrenia,Oppositional Defiant Disorder,Attention Deficit-Hyperactivity Disorder,Autism Spectrum Disorder,Bulimia Nervosa,Anxiety,Autism |
4iar_a | P28222 | ENSG00000135312 | HTR1B | 99.50 | 4.10E-19 | 5.10E-23 | 178.70 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | LTB4R |
LTB4R |
Cavia porcellus | 5x33_a | Q9WTK1 | 99.60 | 1.00E-19 | 1.20E-23 | 194.00 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | 0 | ||||
YDL035C | GPR1 | SGDID:S000002193 | EDNRB ETRB |
Endothelin receptor type B (ET-B) (ET-BR) (Endothelin receptor non-selective type) |
Homo sapiens | Megacolon,Heart Disease,Autosomal Dominant Polycystic Kidney Disease,Intestinal Pseudo-Obstruction,Hepatopulmonary Syndrome,Mitochondrial Dna Depletion Syndrome 12a,Ritter'S Disease,Vascular Disease,Migraine With Or Without Aura 1,Pyoderma,Impotence,Polycystic Kidney Disease,Optic Nerve Disease,Waardenburg'S Syndrome,Connective Tissue Disease,Tietz Albinism-Deafness Syndrome,Transient Refractive Change,Rare Genetic Deafness,Constipation,Stroke, Ischemic,Chronic Pulmonary Heart Disease,Radiation Proctitis,Intestinal Obstruction,Dilated Cardiomyopathy,Waardenburg Syndrome, Type 2d,Migraine With Aura,Impetigo,Cochlear Disease,Scarlet Fever,Oral Cavity Cancer,Peripheral Demyelinating Neuropathy, Central Dysmyelination, Waardenburg Syndrome, And Hirschsprung Disease,Cystic Kidney Disease,Kidney Disease,Perinephritis,Double Pterygium,Waardenburg Syndrome, Type 4b,Waardenburg Syndrome, Type 4c,Pyomyositis,Waardenburg Syndrome Type 4,Pulmonary Arterial Hypertension Associated With Connective Tissue Disease,Gingival Overgrowth,Portal Hypertension,Acquired Color Blindness,Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna,Salivary Gland Disease,Autosomal Recessive Non-Syndromic Sensorineural Deafness Type Dfnb,Acute Poststreptococcal Glomerulonephritis,Goldberg-Shprintzen Syndrome,Waardenburg Syndrome, Type 4a,Piebald Trait,Prostate Cancer,Disease Of Mental Health,Pulmonary Hypertension,Raynaud Disease,Mowat-Wilson Syndrome,Commensal Bacterial Infectious Disease,Intraocular Pressure Quantitative Trait Locus,Waardenburg Syndrome, Type 2e,Waardenburg Syndrome, Type 2c,Diaphragmatic Hernia, Congenital,Hirschsprung Disease 1,Coffin-Lowry Syndrome,Chromosome 17q12 Duplication Syndrome,Waardenburg Syndrome, Type 1,Waardenburg Syndrome, Type 2a,Podoconiosis,Hypertension, Essential,Lipoprotein Quantitative Trait Locus,Aganglionosis, Total Intestinal,Crest Syndrome,Waardenburg Syndrome, Type 3,Intracranial Berry Aneurysm,Central Hypoventilation Syndrome, Congenital,Hirschsprung Disease 2,Abcd Syndrome |
6igk_a | P24530 | ENSG00000136160 | EDNRB | 99.60 | 8.50E-20 | 1.00E-23 | 191.40 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | lpar6a lpar6 zgc:153784 |
lpar6a lpar6 zgc:153784 |
Danio rerio | 5xsz_a | Q08BG4 | 99.60 | 1.40E-19 | 1.80E-23 | 188.00 | 0 | 0 | 0 | 1 | 0 | 0 | 0 | 0 | ||||
YDL035C | GPR1 | SGDID:S000002193 | CHRM1 |
Muscarinic acetylcholine receptor M1 |
Homo sapiens | Alzheimer Disease,Disease Of Mental Health,Heart Block, Congenital,Schizophrenia,Attention Deficit-Hyperactivity Disorder |
5cxv_a | P11229 | ENSG00000168539 | CHRM1 | 99.60 | 1.50E-19 | 1.70E-23 | 193.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | CCR2 CMKBR2 |
C-C chemokine receptor type 2 (C-C CKR-2) (CC-CKR-2) (CCR-2) (CCR2) (Monocyte chemoattractant protein 1 receptor) (MCP-1-R) (CD antigen CD192) |
Homo sapiens | Cytomegalovirus Retinitis,Acquired Immunodeficiency Syndrome,Epidermolytic Acanthoma,Diabetes Mellitus,Autoimmune Disease Of The Nervous System,Myocardial Infarction,Transient Cerebral Ischemia,Acute Hemorrhagic Encephalitis,Arthritis,Idiopathic Anterior Uveitis,Interstitial Lung Disease,Tenosynovial Giant Cell Tumor,Human Immunodeficiency Virus Type 1,Macular Degeneration, Age-Related, 1,Serous Labyrinthitis,Disease Of Mental Health,Pulmonary Fibrosis, Idiopathic,Rheumatoid Arthritis,Multiple Sclerosis,Secondary Progressive Multiple Sclerosis,Duodenum Adenoma,Autoimmune Disease Of Central Nervous System,Hypertension, Essential,Systemic Lupus Erythematosus |
5t1a_a | P41597 | ENSG00000121807 | CCR2 | 99.60 | 4.20E-20 | 5.10E-24 | 195.30 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | CHRM4 |
Muscarinic acetylcholine receptor M4 |
Homo sapiens | Arthrogryposis, Distal, Type 1a,Ureterolithiasis,Cone-Rod Dystrophy 2,Disease Of Mental Health |
5dsg_a | P08173 | ENSG00000180720 | CHRM4 | 99.50 | 4.80E-19 | 5.90E-23 | 180.50 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | ADORA2A ADORA2 |
Adenosine receptor A2a |
Homo sapiens | Migraine With Or Without Aura 1,Status Epilepticus,Basal Ganglia Disease,Stroke, Ischemic,Intermittent Asthma,Dilated Cardiomyopathy,Conduct Disorder,Migraine With Aura,Ataxia, Sensory, 1, Autosomal Dominant,Sleep Disorder,Acute Encephalopathy With Biphasic Seizures And Late Reduced Diffusion,Parkinson Disease, Late-Onset,Adenosine Deaminase Deficiency,Panic Disorder,Disease Of Mental Health,Schizophrenia,Malaria,Gilles De La Tourette Syndrome,Hematuria, Benign Familial,Huntington Disease,Attention Deficit-Hyperactivity Disorder,Parkinson Disease 8, Autosomal Dominant,Hypertension, Essential,Autism Spectrum Disorder,Anxiety,Autism,Asthma |
3eml_a | P29274 | ENSG00000128271 | ADORA2A | 99.50 | 2.20E-19 | 2.70E-23 | 188.60 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | PTGDR2 CRTH2 DL1R GPR44 |
Prostaglandin D2 receptor 2 (Chemoattractant receptor-homologous molecule expressed on Th2 cells) (G-protein coupled receptor 44) (CD antigen CD294) |
Homo sapiens | Conjunctivitis,Bronchial Disease,Folliculitis,Chronic Urticaria,Chronic Spontaneous Urticaria,Nasal Cavity Disease,Eosinophilic Pustular Folliculitis,Nose Disease,Common Cold,Pneumothorax, Primary Spontaneous,Dermatitis, Atopic,Allergic Conjunctivitis,Esophagitis, Eosinophilic, 1,Diclofenac Allergy,Dermatitis, Atopic, 5,Timothy Grass Allergy,Apricot Allergy,Asthma |
6d26_a | Q9Y5Y4 | ENSG00000183134 | PTGDR2 | 99.60 | 1.00E-19 | 1.30E-23 | 188.20 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | F2R CF2R PAR1 TR |
Proteinase-activated receptor 1 (PAR-1) (Coagulation factor II receptor) (Thrombin receptor) |
Homo sapiens | Heart Disease,Myocardial Infarction,Stroke, Ischemic,Orofacial Granulomatosis,Hemorrhagic Disease,Blood Platelet Disease,Blood Coagulation Disease,Glanzmann Thrombasthenia,Ovarian Cancer,Carotid Artery Thrombosis,Prostate Cancer,Bernard-Soulier Syndrome,Thrombocytopenia,Inflammatory Bowel Disease,Hypertension, Essential,Bleeding Disorder, Platelet-Type, 20,Thrombosis,Asthma |
3vw7_a | P25116 | ENSG00000181104 | F2R | 99.60 | 1.10E-20 | 1.30E-24 | 196.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | |
YDL035C | GPR1 | SGDID:S000002193 | P2RY12 HORK3 |
P2Y purinoceptor 12 (P2Y12) (ADP-glucose receptor) (ADPG-R) (P2T(AC)) (P2Y(AC)) (P2Y(cyc)) (P2Y12 platelet ADP receptor) (P2Y(ADP)) (SP1999) |
Homo sapiens | Heart Disease,Diabetes Mellitus,Coronary Thrombosis,Myocardial Infarction,Stroke, Ischemic,Hemorrhagic Disease,Blood Coagulation Disease,Cardiovascular System Disease,Left Bundle Branch Hemiblock,Heart Conduction Disease,Intermediate Coronary Syndrome,Clopidogrel Resistance,Alacrima, Achalasia, And Mental Retardation Syndrome,Bleeding Disorder, Platelet-Type, 8,Disease Of Mental Health,Cerebral Arterial Disease,Bernard-Soulier Syndrome,Thrombocytopenia,Type 2 Diabetes Mellitus,Hermansky-Pudlak Syndrome,Aspirin Allergy,Bleeding Disorder, Platelet-Type, 18,Bleeding Disorder, Platelet-Type, 11,Peripheral Artery Disease,Lipoprotein Quantitative Trait Locus,Nizon-Isidor Syndrome,Thrombosis,Ceroid Lipofuscinosis, Neuronal, 5,Asthma |
4pxz_a | Q9H244 | ENSG00000169313 | P2RY12 | 99.50 | 1.90E-19 | 2.30E-23 | 186.00 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | 0 |