2151
|
|
|
Protein phosphatase targeting COQ7 |
TA-PP2C, TAPP2C |
Curated: N/A
Unreviewed: Mitochondrial Diseases
|
2152
|
|
|
Peptidylprolyl isomerase domain and WD repeat containing 1 |
- |
Curated: Tourette syndrome
Unreviewed: Neuroendocrine Tumors, Osteoporosis, Renal cell carcinoma
|
2153
|
|
|
Pancreatic polypeptide |
PH, PNP, PP |
Curated: N/A
Unreviewed: Adenosine Deaminase Deficiency, Agammaglobulinemia, Alzheimer disease, Amyloidosis, Amyotrophic lateral sclerosis, Anemia, Arsenic Encephalopathy, Arteriosclerosis, Ataxia telangiectasia, Atherosclerosis, Autoimmune disease, Autoimmune Diseases, Autoimmune hemolytic anemia, Bladder carcinoma, Bladder Neoplasm, Brain disease, Breast Cancer, Breast Carcinoma, Carcinoid tumor of intestine, Carcinoma, Carcinoma Of The Head And Neck, Carotid Atherosclerosis, Cerebral Angiitis, Cognition disorder, Cognitive disorder, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal neoplasm, Combined molybdoflavoprotein enzyme deficiency, Cyclic Neutropenia, Developmental Delay, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Retinopathy, Endocrine System Diseases, Esophagus Neoplasm, Gastroesophageal Reflux Disease, Glioblastoma, Graft-Vs-Host Disease, Head and neck neoplasm, Hematologic Neoplasms, Hepatocellular carcinoma, Huntington Disease, Hypercalcemia, Hyperinsulinism, Hyperparathyroidism, Hyperuricemia, Hypogammaglobulinemia, Hypoglycemia, Immune System Diseases, Immune Thrombocytopenic Purpura, Immunologic Deficiency Syndromes, Impaired Cognition, Islet Cell Tumor, Lesch-Nyhan Syndrome, Liver carcinoma, Liver failure, Lupus Erythematosus, Lupus Vulgaris, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoma, Lymphopenia, Major depressive disorder, Malignant Neoplasm, Megalencephaly, Polymicrogyria, Polydactyly, Hydrocephalus Syndrome, Melanoma, MELAS Syndrome, Mental retardation, Metabolic Diseases, Metastatic Melanoma, Monoclonal Gammapathies, Motor delay, Multiple Endocrine Neoplasia, Myotonic dystrophy, Neoplasms, Nervous System Disorder, Neuroblastoma, Neurodegenerative Disorders, Neuroendocrine Tumors, Obesity, Omenn Syndrome, Osteoporosis, Otitis media, Ovarian neoplasm, Pachyonychia Congenita, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic Diseases, Pancreatic Neoplasm, Pancreatitis, Paraganglioma, Parkinson disease, Periodontal Diseases, Periodontitis, Phosphoribosylpyrophosphate Synthetase Superactivity, Polyneuropathy, Prostate cancer, Prostatic neoplasm, Prostatic Neoplasms, Purine-Nucleoside Phosphorylase Deficiency, Retinal Vein Occlusion, Sepsis, Severe combined immunodeficiency disease, Sinusitis, Skin Lesion, Spastic diplegia, Spastic tetraparesis, Systemic lupus erythematosus, T-cell leukemia, T-Cell Lymphoma, Urinary bladder cancer, Urinary bladder neoplasms, Vascular Diseases, ZAP70 Deficiency, Zollinger-Ellison syndrome
|
2154
|
|
|
Pancreatic polypeptide 2, pseudogene |
PPY2 |
Curated: N/A
Unreviewed: N/A
|
2155
|
|
|
Polyglutamine binding protein 1 |
MRX2, MRX55, MRXS3, MRXS8, NPW38, RENS1, SHS |
Curated: Atrial septal defect, Autism, Growth disorder, Congenital heart septal defect, Intellectual developmental disorder, Microcephaly, Hereditary spastic paraplegia, Diabetes mellitus type 2, X-linked intellectual disability, renpenning syndrome
Unreviewed: Anxiety Disorder, Arachnodactyly, Asthma, Atrial Septal Defect, Brachycephaly, Breast neoplasm, Camptodactyly of fingers, Cataract, Cerebral Atrophy, Charcot-Marie-Tooth disease, Coffin-Lowry Syndrome, Colorectal Cancer, Congenital Camptodactyly, Congenital Epicanthus, Congenital Microcephaly, Congenital ocular coloboma, Congenital Pectus Excavatum, Coronary artery disease, Development Disorder, Developmental Delay, Developmental disability, Dwarfism, Dysmorphic Features, Dysmorphism, Epilepsy, Fatty Liver, Hamel Cerebro-Palato-Cardiac Syndrome, Hereditary spastic paraplegia, X-linked, High palate, Hyperopia, Hypospadias, Impaired Cognition, Imperforate anus, Macroglossia, Macrotia, Malocclusion, Mental retardation, Mental Retardation, X-Linked, Micrognathism, Microlissencephaly, Microphthalmos, Microstomia, Motor Neuron Disease, Nail dystrophy, Nervous System Disorder, Neurodegenerative Disorders, Osteosarcoma, Parkinson disease, Partial Agenesis Of Corpus Callosum, Persistent Ostium Primum, Renpenning Syndrome, Scoliosis, Secundum atrial septal defect, Situs Inversus, Spastic diplegia, Spastic paraplegia, Spinocerebellar Ataxia, Strabismus, Sveinsson chorioretinal atrophy, Tetralogy of Fallot, Trichohepatoenteric Syndrome, Ventricular septal defect
|
2156
|
|
|
PRAC1 small nuclear protein |
C17orf92, PRAC |
Curated: Psoriasis
Unreviewed: Benign Prostatic Hyperplasia, Colonic disease, Colorectal neoplasm, Prostate cancer, Prostatic neoplasm, Renal cell carcinoma
|
2157
|
|
|
PRAC2 small nuclear protein |
C17orf93, HOXB-AS5, HOXB13-AS1, HOXBAS5, NCRNA00253 |
Curated: N/A
Unreviewed: Breast Cancer, Breast Carcinoma, Breast neoplasm, Glioma, Neoplasms, Papillary thyroid cancer, Prostate cancer, Prostatic neoplasm, Thyroid cancer
|
2158
|
|
|
Protease associated domain containing 1 |
C2orf7, PAP21 |
Curated: N/A
Unreviewed: Colorectal neoplasm, Pyelonephritis
|
2159
|
|
|
Protease associated domain containing 1 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
|
2160
|
|
|
PRC2 and DDX5 associated lncRNA |
- |
Curated: N/A
Unreviewed: N/A
|