2771
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Cytoplasmic polyadenylation element binding protein 4 |
CPE-BP4, hCPEB-4 |
Curated: Ankylosing spondylitis, Atrial fibrillation, Atrial flutter, Attention deficit hyperactivity disorder, Cardiovascular disease, Obstructive pulmonary disease, Crohn disease, Hypertension, Gout, Heart failure, Inflammatory bowel disease, Multiple myeloma, Obesity, Peptic ulcer disease, Prion disease, Psoriasis, Sclerosing cholangitis, Sjogren syndrome, Skin disease, Substance abuse, Ulcerative colitis, Uterine prolapse
Unreviewed: Adenocarcinoma, Ankylosing Spondylitis, Astrocytoma, Autism Spectrum Disorder, B-Cell Lymphoma, Breast Cancer, Breast Carcinoma, Carcinoma Of The Head And Neck, Cholangitis, Cirrhosis, Colorectal Cancer, Colorectal neoplasm, Crohn Disease, Gallbladder cancer, Gallbladder neoplasm, Glioblastoma, Glioma, Hepatocellular carcinoma, Huntington disease, Inflammatory Bowel Disease, Liver Cancer, Liver carcinoma, Liver Cirrhosis, Lung carcinoma, Lung neoplasms, Malignant Neoplasm, Melanoma, Neoplasms, Non-Alcoholic Fatty Liver Disease, Pancreatic adenocarcinoma, Patent ductus arteriosus, Portal Hypertension, Skin neoplasm, Stomach Carcinoma, Stomach Neoplasms
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2772
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Cadherin like and PC-esterase domain containing 1 |
C7orf58 |
Curated: Ankle fracture, Bone fracture, Creutzfeldt-jakob disease, Diabetes mellitus type 2, Upper extremity fracture, Uterine fibroid
Unreviewed: Anxiety Disorder, Autism, Becker Muscular Dystrophy, Breast Cancer, Breast Carcinoma, Breast neoplasm, Coffin-Siris Syndrome, Creutzfeldt-Jakob Disease, Diabetes Mellitus, Lymphatic metastasis, Obesity, Osteoporosis, Vitelliform Macular Dystrophy
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2773
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Ceruloplasmin and hephaestin like 1, pseudogene |
CPHL1 |
Curated: N/A
Unreviewed: N/A
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2774
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Cytoplasmic polyadenylated homeobox like |
CPHXL1 |
Curated: N/A
Unreviewed: N/A
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2775
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Cytoplasmic polyadenylated homeobox like 2 |
- |
Curated: N/A
Unreviewed: N/A
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2776
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Ciliogenesis and planar polarity effector complex subunit 1 |
C5orf42, Hug, JBTS17, OFD6 |
Curated: Monomelic amyotrophy, Desbuquois syndrome, Encephalocele, Aplasia of the vermis, Global developmental delay, Hodgkin lymphoma, Joubert syndrome, Nephronophthisis, Orofaciodigital syndrome, Polydactyly, Retinitis pigmentosa, Uranostaphyloschisis, joubert syndrome 17
Unreviewed: Anemia, Brachydactyly, Cerebellar vermis agenesis, Ciliopathies, Clinodactyly, Congenital abnormalities, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital Epicanthus, Congenital heart defects, Craniocerebral trauma, Cryptorchidism, Developmental Delay, Disorder Of Eye, Distal upper limb amyotrophy, Dwarfism, Dysmorphic Features, Esotropia, Frontal bossing, Glaucoma, Hearing Loss, High palate, Hirschsprung Disease, Holoprosencephaly, Hydatidiform mole, Hydrocephalus, Hypothalamic Hamartomas, Intellectual developmental disorder, Joubert Syndrome, Malformation of cortical development, Meckel-gruber syndrome, Mental retardation, Microcephaly, Micrognathism, Monomelic Amyotrophy, Multiple Congenital Anomalies, Nystagmus, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Oral cleft, Osteofibrous Dysplasia, Polydactyly Of Toes, Polymicrogyria, Posteriorly Rotated Ear, Psychotic disorders, Ptosis, Radial Polydactyly, Renal agenesis, Renal dysplasia, Schizophrenia, Scoliosis, Situs Inversus, Strabismus, Syndactyly, Syndactyly Of The Toes, Vitelliform Macular Dystrophy
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2777
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CPLANE1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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2778
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Ciliogenesis and planar polarity effector complex subunit 2 |
C1orf89, RSG1 |
Curated: N/A
Unreviewed: Atherosclerosis, Ciliopathies, Ciliopathy, Cleft palate, Hereditary Hemochromatosis, Orofaciodigital syndrome, Polydactyly
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2779
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Complexin 1 |
CPX-I, CPX1, DEE63, EIEE63 |
Curated: Behcet disease, Bipolar disorder, Bipolar depression, Major depressive disorder, Developmental and epileptic encephalopathy, Infantile myoclonic epilepsy, Psychotic disorders, Schizophrenia, Vasculitis, Wolff-parkinson-white syndrome
Unreviewed: Absence Of Septum Pellucidum, Alzheimer disease, Anxiety Disorder, Ataxia, Atrial fibrillation, Attention Deficit Hyperactivity Disorder, Axenfeld anomaly, Behcet Syndrome, Bipolar Disorder, Brain disease, Cerebellar diseases, Congenital anomaly of eye, Congenital Clubfoot, Congenital Epicanthus, Cryptorchidism, Dementia, Developmental Delay, Developmental disability, Developmental regression, Diabetes Mellitus, Diabetes mellitus, type 2, Dwarfism, Dysarthria, Epilepsy, Epileptic encephalopathy, Febrile seizures, Gastroesophageal Reflux Disease, Gestational diabetes, Hemangioma, Hereditary Leber Optic Atrophy, Hypodontia, Hypospadias, Immunologic Deficiency Syndromes, Impaired Cognition, Language Disorders, Manic Disorder, Mental Depression, Mental retardation, Microcephaly, Micrognathism, Myoclonic Epilepsy, Myoclonic Seizures, Nystagmus, Obesity, Parkinson disease, Photosensitive tonic-clonic seizures, Pitt-Rogers-Danks Syndrome, Precocious puberty, Proptosis, Psychosis, Ptosis, Radioulnar Synostosis, Rib fusion, Rieger syndrome, Schizoaffective Disorder, Schizophreniform Disorders, Scoliosis, Stenosis Of External Auditory Canal, Stereotyped Behavior, Strabismus, Ventricular septal defect, Wolf-Hirschhorn Syndrome
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2780
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Complexin 2 |
921-L, CPX-2, CPX2, Hfb1 |
Curated: Attention deficit hyperactivity disorder, Bipolar disorder, Color vision deficiency, Bipolar depression, Major depressive disorder, Insomnia, Obesity, Psychotic disorders, Schizophrenia
Unreviewed: Alzheimer disease, Atrophy, Attention Deficit Hyperactivity Disorder, Bipolar Disorder, Brain disease, Brain injuries, Breast neoplasm, Cognition disorder, Dementia, Glioma, Huntington Disease, Impaired Cognition, Manic Disorder, Mental Depression, Myocardial Infarction, Nervous System Disorder, Proximal symphalangism, Psychosis, Schizoaffective Disorder, Schizophreniform Disorders, Stomach neoplasms
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