1191
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|
|
Neurturin |
NTN |
Curated: Alzheimer disease, Hirschsprung disease
Unreviewed: Acoustic Neuroma, Adrenal Gland Pheochromocytoma, Breast neoplasm, Colonic Aganglionosis, Diabetes, Diabetes Mellitus, Dwarfism, Encephalitis, Hearing Loss, Hepatocellular carcinoma, Hirschsprung Disease, Hyperglycemia, Intestinal Obstruction, Intestinal Polyposis, Liver cirrhosis, Mental Depression, Mental retardation, Movement Disorders, Neoplasms, Neurodegenerative Disorders, Neuropathy, Pancreatic cancer, Pancreatic carcinoma, Paraganglioma, Parkinson disease, Pheochromocytoma, Psoriasis, Thyroid Neoplasm
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1192
|
|
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Neurexin 1 |
Hs.22998, PTHSL2, SCZD17 |
Curated: Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Biliary tract cancer, Bipolar disorder, Central nervous system cancer, Cervical cancer, Chromosome 2p16.3 deletion syndrome, Color vision deficiency, Neurodevelopmental disorder, Coronary artery disease, Craniofacial abnormalities, Dementia, Major depressive disorder, Dry eye syndrome, Dyslexia, Eosinophilia, Glioma, Global developmental delay, Glomerulonephritis, Gout, Insomnia, Intellectual developmental disorder, Internet addiction disorder, Language development disorders, Metabolic syndrome, Intellectual disability, Microcephaly, Myocardial infarction, Non-specific syndromic intellectual disability, Obesity, Osteoarthritis, Schizophrenia, Scoliosis, Substance abuse, Hypertension, Diabetes mellitus type 2, complex neurodevelopmental disorder
Unreviewed: Amyotrophic Lateral Sclerosis, Asperger Syndrome, Attention Deficit Hyperactivity Disorder, Auditory processing disorder, Autism spectrum disorder, Bipolar Disorder, Brachycephaly, Brain disease, Breast neoplasm, Celiac disease, Cerebral cortical atrophy, CHARGE Syndrome, CHROMOSOME 2p16.3 DELETION SYNDROME, Cognitive disorder, Colorectal neoplasm, Congenital abnormalities, Congenital Chromosomal Disease, Cryptorchidism, Development Disorder, Developmental Delay, Developmental disability, Developmental regression, Diabetes Mellitus, Dysmorphic Features, Dysphagia, Epilepsy, Epileptic encephalopathy, Esophageal squamous cell carcinoma, Fanconi anemia, Fragile X Syndrome, Frontal bossing, Gastroesophageal Reflux Disease, Gestational diabetes, Gluten intolerance, Gonadal dysgenesis, Hirschsprung disease, Impaired Cognition, Intracranial aneurysm, Language Development Disorders, Learning disorders, Lung neoplasms, Lymphoblastic Leukemia, Lymphocytic Leukemia, Macrostomia, Malocclusion, Mental Depression, Mental Disorders, Mental retardation, Multiple Congenital Anomalies, Multiple Sclerosis, Myeloid leukemia, Narcolepsy, Nasopharyngeal carcinoma, Neurodevelopmental Disorders, Night blindness, congenital stationary, Nonorganic Psychosis, Pitt-Hopkins Syndrome, Pitt-Hopkins-Like Syndrome, Plagiocephaly, Precocious puberty, Prostatic neoplasm, Psychosis, Psychotic disorders, Pulmonary Stenosis, Sarcoma, Social Communication Disorder, Specific Language Impairment, Speech Delay, Stereotyped Behavior, Stomach neoplasms, Strabismus, Temporal lobe epilepsy, Thyroid cancer, Tourette Syndrome, Tricuspid Valve Insufficiency, Ventricular septal defect
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1193
|
|
|
NRXN1 divergent transcript |
- |
Curated: N/A
Unreviewed: N/A
|
1194
|
|
|
Neurexin 2 |
- |
Curated: Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Epilepsy, Developmental and epileptic encephalopathy, Gout, Intellectual developmental disorder, Neurodevelopmental disorder, Schizophrenia, Substance abuse, Diabetes mellitus type 2, complex neurodevelopmental disorder
Unreviewed: Amnesia, Autism spectrum disorder, Developmental Delay, Gouty arthritis, Leukocyte adhesion deficiency, Mental retardation, Migraine, Neurodevelopmental Disorders, Parkinson disease, Prion disease, Spinal Muscular Atrophy, Thyroid cancer
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1195
|
|
|
NRXN2 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: Gout, Gouty arthritis
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1196
|
|
|
Neurexin 3 |
C14orf60 |
Curated: Alzheimer disease, Amyotrophic lateral sclerosis, Atrial fibrillation, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Breast cancer, Color vision deficiency, Colorectal cancer, Coronary aneurysm, Crohn disease, Dementia, Diabetes mellitus, Diabetic eye disease, Diabetic neuropathy, Diabetic retinopathy, Heart failure, Hypertension, Idiopathic pulmonary fibrosis, Inflammatory bowel disease, Insomnia, Major depressive disorder, Metabolic syndrome, Nasal disorder, Obesity, Obstructive sleep apnea syndrome, Oligodendroglioma, Pancreatic cancer, Proliferative diabetic retinopathy, Prostate cancer, Schizoaffective disorder, Schizophrenia, Squamous cell carcinoma, Substance abuse, Diabetes mellitus type 2
Unreviewed: Adenocarcinoma, Adenoma, Autism spectrum disorder, Bipolar Disorder, Borderline personality disorder, Brain disease, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinogenesis, Central nervous system disease, Cholelithiasis, Chromosomal instability, Cognitive disorder, Congenital abnormalities, Developmental disability, Diabetes Mellitus, Epilepsy, Epileptic encephalopathy, Facial dysmorphism, Facial dysmorphism syndrome, Glioblastoma, Glioma, Graves Disease, Hepatocellular carcinoma, Hirschsprung disease, Impaired Cognition, Lateral Sclerosis, Macrocephaly, Mental retardation, Myeloid leukemia, Nasopharyngeal carcinoma, Neurodevelopmental Disorders, Pancreatic neoplasm, Renal Carcinoma, Schizoaffective Disorder, Tauopathies
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1197
|
|
|
NRXN3 antisense RNA 1 |
- |
Curated: N/A
Unreviewed: N/A
|
1198
|
|
|
NRXN3 antisense RNA 2 |
- |
Curated: N/A
Unreviewed: N/A
|
1199
|
|
|
NRXN3 antisense RNA 3 |
- |
Curated: N/A
Unreviewed: N/A
|
1200
|
|
|
NSA2 ribosome biogenesis factor |
CDK105, HCL-G1, HCLG1, HUSSY-29, HUSSY29, TINP1 |
Curated: Biliary cirrhosis, Liver cirrhosis, Biliary cholangitis
Unreviewed: Biliary Cholangitis, Carcinogenesis, Diabetes, Diabetes Mellitus, Diabetic Nephropathy, Glioblastoma, Hairy Cell Leukemia, Hyperglycemia, Kidney Disease, Neoplasms
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