2441
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Contactin associated protein 1 |
CASPR, CHN3, CNTNAP, NRXN4, P190 |
Curated: Arthrogryposis multiplex congenita, Distal arthrogryposis, Breast cancer, Charcot-marie-tooth disease, Congenital deformity of clavicle, Congenital deformity of elbow, Congenital deformity of forearm, Congenital deformity of scapula, Congenital deformity of wrist, Congenital dislocation of elbow, Congenital glenohumeral joint dislocation, Lethal congenital contracture syndrome, Major depressive disorder, Neuropathy, congenital hypomyelinating, Pena-shokeir syndrome
Unreviewed: Adenocarcinoma, Arthrogryposis, Astrocytoma, Atrophy Of Corpus Callosum, Autism, B-cell Lymphoma, Blast crisis, Blast phase chronic myelogenous leukemia, Bone disease, Breast Carcinoma, Bulbar palsy, Cerebellar atrophy, Cerebral Atrophy, Cerebral cortical atrophy, Congenital Epicanthus, Congenital Hypomyelinating Neuropathy, Congenital muscular dystrophy, Contracture, Demyelinating diseases, Demyelinating neuropathy, Developmental disability, Dolichocephaly, Dyslexia, Dysphagia, Dystonia, Frontal bossing, Gastroesophageal Reflux Disease, Guillain-Barre Syndrome, Heart disease, Hemangioma, Hematologic neoplasm, Hematologic Neoplasms, Hepatitis b, High palate, Hydrocephalus, Hypomyelination Neuropathy-Arthrogryposis Syndrome, Hypoplasia Of Corpus Callosum, Hypotonia, Intellectual developmental disorder, Lethal Congenital Contracture Syndrome, Leukemia, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoid leukemia, Lymphoma, Malignant lymphoma, lymphocytic, intermediate differentiation, Malignant Neoplasm, Mantle Cell Lymphoma, Mental Depression, Microcephaly, Micrognathism, Monocytic Leukemia, Monocytosis, Multiple Sclerosis, Myelodysplastic Syndrome, Myelofibrosis, Myeloid Leukemia, Myelomonocytic Leukemia, Myeloproliferative disorder, Myopathy, Neoplasms, Nervous System Diseases, Neurodegenerative disorder, Neurodevelopmental Disorders, Neuropathy, Oligodendroglioma, Optic Atrophy, Oropharyngeal Dysphagia, Pena Shokeir syndrome, Peripheral nervous system disease, Promyelocytic Leukemia, Ptosis, Renal cell carcinoma, Spinal Muscular Atrophy, Thrombocythemia, Tremor
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2442
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CNTNAP1 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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2443
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|
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Contactin associated protein 2 |
AUTS15, CASPR2, CDFE, NRXN4, PTHSL1 |
Curated: Alzheimer disease, Asthma, Autism, Bipolar disorder, Breast cancer, Cataract, Charcot-marie-tooth disease, Developmental and epileptic encephalopathy, Colorectal cancer, Colonic neoplasms, Neurodevelopmental disorder, Cortical dysplasia-focal epilepsy syndrome, Crohn disease, Dementia, Diabetic neuropathy, Epilepsy, Rolandic epilepsy, Gastroesophageal reflux disease, Glaucoma, Gout, Hyperkinesia, Idiopathic pulmonary fibrosis, Inflammatory bowel disease, Intellectual developmental disorder, Irritable bowel syndrome, Language development disorders, Major depressive disorder, Metabolic syndrome, Nonalcoholic fatty liver disease, Non-specific syndromic intellectual disability, Obesity, Oligodendroglioma, Parkinson disease, Peptic ulcer disease, Prostate cancer, Psychiatric disorders, Willis-ekbom disease, Schizophrenia, Scoliosis, Small cell lung carcinoma, Specific language disorder, Diabetes mellitus type 2, Ulcerative colitis, Depression, Vascular dementia, complex neurodevelopmental disorder
Unreviewed: Acquired Neuromyotonia, Androgen-Insensitivity Syndrome, Aphasia, Apraxia, Atrial Septal Defect, Atrophy, Attention Deficit Hyperactivity Disorder, Auditory processing disorder, Autism spectrum disorder, Autoimmune Diseases, Bipolar Disorder, Brachycephaly, Brain disease, Breast neoplasm, Celiac disease, Cerebral cortical atrophy, Chronic pain, Cirrhosis, Congenital abnormalities, Cortical development malformation, Cortical Dysplasia, Cortical Dysplasia With Focal Epilepsy Syndrome, Cortical Dysplasia-Focal Epilepsy Syndrome, Cryptorchidism, Developmental Delay, Developmental disability, Developmental dyslexia, Diabetes mellitus, Diabetic foot, Dyslexia, Dysphagia, Encephalitis, Epileptic encephalopathy, Exfoliation Syndrome, Exostoses, Focal cortical dysplasia, Frontal bossing, Frontotemporal dementia, Gastroesophageal Reflux Disease, Glioma, Gluten intolerance, Hereditary xerocytosis, Hypertension, Immune System Diseases, Impaired Cognition, Isaacs Syndrome, Language Development Disorders, Language Disorders, Laryngeal Carcinoma, Learning disorders, Liver Cirrhosis, Lung carcinoma, Lupus Erythematosus, Malformation of cortical development, Malnutrition, Malocclusion, Memory Disorders, Mental Depression, Mental Disorders, Mental retardation, Metastatic Melanoma, Movement Disorders, Multiple Sclerosis, Myasthenia Gravis, Neoplasms, Nervous System Disorder, Neurodevelopmental Disorders, Neuromuscular disease, Neuroticism, Obsessive-Compulsive Disorder, Ovarian Failure, Pancreatic neoplasm, Parkinson Disease, Partial epilepsy, Peripheral nervous system disease, Pitt-Hopkins Syndrome, Pitt-Hopkins-Like Syndrome, Plagiocephaly, Precocious puberty, Premature Menopause, Psychosis, Pulmonary Stenosis, Rhabdoid Tumor, Seizure, Seizures, Sleep Disorders, Social Communication Disorder, Specific Language Impairment, Speech Delay, Speech Disorders, Stammering, Stereotyped Behavior, Strabismus, Stuttering, Tauopathies, Temporal lobe epilepsy, Thymoma, Tourette Syndrome, Tricuspid Valve Insufficiency, Ventricular septal defect
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2444
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CNTNAP2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
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2445
|
|
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Contactin associated protein family member 3 |
CASPR3, CNTNAP3A |
Curated: N/A
Unreviewed: Atrial Septal Defect, Autism Spectrum Disorder, Bladder Exstrophy, Crohn disease, Schizophrenia, Stomach neoplasms
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2446
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|
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Contactin associated protein family member 3B |
- |
Curated: N/A
Unreviewed: N/A
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2447
|
|
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Contactin associated protein family member 3C |
- |
Curated: N/A
Unreviewed: N/A
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2448
|
|
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CNTNAP3 pseudogene 1 |
- |
Curated: N/A
Unreviewed: N/A
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2449
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CNTNAP3 pseudogene 2 |
- |
Curated: N/A
Unreviewed: N/A
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2450
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CNTNAP3 pseudogene 3 |
- |
Curated: N/A
Unreviewed: N/A
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