2281
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Phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2 |
DEP.2, DEPDC2, P-REX2, PPP1R129 |
Curated: Cerebral arteriovenous malformations, Bladder exstrophy, Dry eye syndrome, Pancreatic cancer
Unreviewed: Alzheimer disease, Basal cell carcinoma, Bladder Exstrophy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Chronic obstructive pulmonary disease, Colorectal Cancer, Febrile seizures, Gastritis, Generalized epilepsy with febrile seizures plus, Hepatocellular carcinoma, Lip and Oral Cavity Carcinoma, Liver Cancer, Liver carcinoma, Malignant Neoplasm, Melanoma, Myeloid leukemia, Neoplasms, Pancreatic adenocarcinoma, Seizures, Stomach neoplasms, Triple negative breast cancer
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2282
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Perforin 1 |
HPLH2, P1, PFP |
Curated: Aplastic anemia, Autism, Autoinflammatory syndrome, Crohn disease, Hemophagocytic lymphohistiocytosis, Hereditary hemophagocytic lymphohistiocytosis, Multiple sclerosis, Nonalcoholic fatty liver disease
Unreviewed: N/A
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2283
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- |
- |
Curated: N/A
Unreviewed: N/A
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2284
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Proteoglycan 2, pro eosinophil major basic protein |
BMPG, MBP, MBP1, proMBP |
Curated: Alzheimer disease, Autism
Unreviewed: Ablepharon macrostomia syndrome, Adrenoleukodystrophy, Amnesia, Amyloidosis, Amyotrophic Lateral Sclerosis, Anemia, Anorexia, Arthropathy, Asthma, Astrocytoma, Atopic dermatitis, Aural Atresia, Congenital, Autoimmune disease, Autoimmune Diseases, B-Cell Lymphoma, Behcet disease, Benign mucous membrane pemphigoid, Bipolar disorder, Blister, Bone Marrow Diseases, Brain infarction, Brain Neoplasms, Bullous pemphigoid, Cardiovascular Diseases, Central Nervous System Lymphoma, Cerebral amyloid angiopathy, Charcot-Marie-Tooth Disease, CNS Disorder, Cognition disorder, Colon Carcinoma, Colonic Neoplasms, Colorectal neoplasm, Cone-rod dystrophy, Congenital abnormalities, Conjunctivitis, Connective Tissue Disease, Contiguous gene syndrome, Cystic fibrosis, Deficiency Of Glucose-6-Phosphate Dehydrogenase, Demyelinating Diseases, Dermatitis, Developmental Delay, Diabetes Mellitus, Diffuse Lymphoma, Down Syndrome, Eczema, Encephalitis, Epileptic encephalopathy, Erectile Dysfunction, Esophageal squamous cell carcinoma, Geographic Atrophy, Glaucoma, Glioblastoma, Glioma, Glomerulonephritis, Growth disorder, Hashimoto disease, Hepatocellular carcinoma, Hereditary Liability To Pressure Palsies, Hodgkin disease, Hyperhomocysteinemia, Hypersensitivity, Hypertension, Hypoxic-Ischemic Encephalopathy, Immunoglobulin A deficiency, Impaired Cognition, Learning Disorders, Leukemia, Leukodystrophy, Leukoencephalopathy, Lupus Erythematosus, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Macular degeneration, Major depressive disorder, Malignant Neoplasm, Mental Depression, Mental Disorders, Mental retardation, Mitral Valve Stenosis, Movement disorder, Multiple Sclerosis, Myasthenia Gravis, Myocarditis, Nasal polyp, Neoplasms, Neurilemmoma, Neurodegenerative Disorders, Neuromyelitis Optica, Non-Hodgkin lymphoma, Obesity, Oligodendroglioma, Optic Neuritis, Osteoglosphonic dysplasia, Otitis media, Panic disorder, Paraplegia, Paratuberculosis, Parkinson disease, Pelizaeus-Merzbacher disease, Peripheral Nerve Sheath Neoplasm, Periventricular Leukomalacia, Phenylketonuria, Polyposis, Progressive myoclonic epilepsy, Prostatic Neoplasms, Psychotic disorders, Retinal Diseases, Retinoblastoma, Rheumatoid arthritis, Rhinitis, Schizophrenia, Sclerosis, Seizures, Skin disease, Sleep apnea, Somatotropin Deficiency, Spinal Cord Diseases, Spinal Muscular Atrophy, Stress Disorder, Stroke, Subarachnoid hemorrhage, Thoracic aortic aneurysm, Thyroid eye disease, Trimethylaminuria, Willis-ekbom disease
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2285
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Proteoglycan 3, pro eosinophil major basic protein 2 |
MBP2, MBPH |
Curated: Hypertrophic cardiomyopathy
Unreviewed: N/A
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2286
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Proteoglycan 4 |
CACP, HAPO, JCAP, MSF, SZP |
Curated: Arthrogryposis multiplex congenita, Camptodactyly-arthropathy-coxa vara-pericarditis syndrome, Contracture, Hyperplasia, Pena-shokeir syndrome , Pericarditis, Secondary malignant neoplasm
Unreviewed: N/A
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2287
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Proline rich protein HaeIII subfamily 1 |
Db-s, PA, PIF-S, PRH2, PRP-1/PRP-2, Pr1/Pr2 |
Curated: N/A
Unreviewed: Arthrogryposis multiplex congenita, Autoimmune disease, Blood coagulation disorder, Blood Coagulation Disorders, Cardiomyopathy, Cerebral palsy, Dental caries, Disseminated Intravascular Coagulation, Hyperlipoproteinemia, Hypertension, Hypertrophic cardiomyopathy, intracranial hypertension, Ischemic Stroke, Liver Fibrosis, Lupus anticoagulant, Myocardial Infarction, Myopathy, Myositis, Protein C Deficiency, Pulmonary Fibrosis, Purpura Fulminans, Septicemia, Stroke, Thrombophilia, Vertical Talus
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2288
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- |
PRH1 |
Curated: N/A
Unreviewed: N/A
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2289
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- |
- |
Curated: N/A
Unreviewed: N/A
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2290
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Proline rich protein HaeIII subfamily 2 |
PRP-1/PRP-2, Pr, pr1/Pr2 |
Curated: N/A
Unreviewed: Arthrogryposis multiplex congenita, Blood Coagulation Disorders, Cardiomyopathy, Cerebral palsy, Dental caries, Disseminated Intravascular Coagulation, Hyperlipoproteinemia, Hypertension, Hypertrophic cardiomyopathy, Ischemic Stroke, Liver Fibrosis, Lupus anticoagulant, Myocardial Infarction, Myopathy, Myositis, Protein C Deficiency, Pulmonary Fibrosis, Purpura Fulminans, Septicemia, Stroke, Thrombophilia, Vertical Talus
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