1231
|
|
|
NOP2/Sun RNA methyltransferase 5 |
NOL1, NOL1R, NSUN5A, WBSCR20, WBSCR20A, p120, p120(NOL1) |
Curated: N/A
Unreviewed: Adenocarcinoma, Aortic aneurysm, Arteriosclerosis, Atherosclerosis, Breast Cancer, Breast Carcinoma, Capillary Malformation-Arteriovenous Malformation, Carcinoma, Cognitive disorder, Colon Carcinoma, Colonic Neoplasms, Colorectal neoplasm, Congenital abnormalities, Ductal Carcinoma, Glioblastoma, Glioma, Impaired Cognition, Invasive Duct and Lobular Carcinoma, Leukemia, Lip and Oral Cavity Carcinoma, Lung Cancer, Lung carcinoma, Malignant Neoplasm, Mucinous Adenocarcinoma, Neoplasms, Pancreatic cancer, Pancreatic carcinoma, Prostatic Diseases, Prostatic neoplasm, Renal cell carcinoma, Stroke, Urologic neoplasm, Williams Syndrome
|
1232
|
|
|
NSUN5 pseudogene 1 |
NSUN5B, WBSCR20B |
Curated: N/A
Unreviewed: N/A
|
1233
|
|
|
NSUN5 pseudogene 2 |
NOL1R2, NSUN5C, WBSCR20B, WBSCR20C |
Curated: N/A
Unreviewed: Hepatocellular carcinoma
|
1234
|
|
|
NOP2/Sun RNA methyltransferase 6 |
4933414E04Rik, ARL5B-AS1, MRT82, NOPD1 |
Curated: Breast neoplasms, Intellectual developmental disorder, Schizophrenia, Scoliosis
Unreviewed: Alzheimer disease, Brain injuries, Breast Cancer, Breast Carcinoma, Cholangiocarcinoma, Colorectal neoplasm, Glioblastoma, Glioma, Mammary Neoplasms, Marfan Syndrome, Pancreatic neoplasm, Renal cell carcinoma, Thyroid cancer
|
1235
|
|
|
NOP2/Sun RNA methyltransferase family member 7 |
- |
Curated: Male infertility, Psoriasis
Unreviewed: Alzheimer disease, Asthenozoospermia, Brain injuries, Hepatocellular carcinoma, Infertility, Liver failure, Liver neoplasm
|
1236
|
|
|
5', 3'-nucleotidase, cytosolic |
DNT, DNT1, HEL74, P5N2, PN-I, PN-II, UMPH2, cdN, dNT-1 |
Curated: Colorectal neoplasms
Unreviewed: Astrocytoma, Attention Deficit Hyperactivity Disorder, Autism, Breast neoplasm, Colon Carcinoma, Colonic Neoplasms, Colorectal Cancer, Colorectal Neoplasms, Common Variable Immunodeficiency, Diabetes, Diabetes Mellitus, Hemolytic anemia, Hepatitis c, Leukemia, Malignant Neoplasm, Mesothelioma, Neoplasms, Oligodendroglioma, Stroke
|
1237
|
|
|
5'-nucleotidase, cytosolic IA |
CN-I, CN-IA, CN1, CN1A, CNI |
Curated: Amyotrophic lateral sclerosis, Lymphocytic leukemia, Metabolic syndrome, Myocardial infarction, Diabetes mellitus type 2
Unreviewed: Arthritis, Autoimmune disease, Autoimmune Diseases, Breast neoplasm, Cyclic Neutropenia, Dermatomyositis, Erectile Dysfunction, Graft-Vs-Host Disease, Graves ophthalmopathy, Heterotaxy, Visceral, Hyperbilirubinemia, Hypertension, Hypoaldosteronism, Inclusion body myopathy, Inclusion Body Myositis, Kidney Disease, Kidney Failure, Leukemia, Leukopenia, Lung Diseases, Lupus Erythematosus, Lupus Nephritis, Malignant Neoplasm, Myositis, Neoplasms, Pancreatic adenocarcinoma, Pancreatic cancer, Pancreatic carcinoma, Pancreatic Neoplasm, Papillary thyroid carcinoma, Polymyositis, Renal Carcinoma, Renal fibrosis, Renal Insufficiency, Scleroderma, Syndromic microphthalmia, Thrombotic Microangiopathies
|
1238
|
|
|
5'-nucleotidase, cytosolic IB |
AIRP, CN-IB, CN1B |
Curated: Atrial fibrillation, Bulimia, Corneal neovascularization, Coronary artery disease, Diverticular disease, Hypertension, Keratitis
Unreviewed: N/A
|
1239
|
|
|
NT5C1B-RDH14 readthrough |
AIRP, NT5C1B, cN-IB, cN1B |
Curated: Cerebellar atrophy, Corneal neovascularization, Intellectual developmental disorder, Keratitis
Unreviewed: Anorexia, Bulimia, Neoplasms
|
1240
|
|
|
5'-nucleotidase, cytosolic II |
GMP, NT5B, PNT5, SPG45, SPG65, cN-II |
Curated: Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Spastic paraplegia, Barrett esophagus, Bipolar disorder, Brain aneurysm, Cannabis abuse, Cardiovascular disease, Hereditary spastic paraplegia, Coronary artery disease, Esophageal disease, Gout, Hypertension, Major depressive disorder, Metabolic syndrome, Migraine, Mood disorder, Myocardial infarction, Neurodevelopmental disorder, Neurotic disorder, Obesity, Obsessive-compulsive disorder, Schizophrenia, Systemic lupus erythematosus, Tourette syndrome, Diabetes mellitus type 2, Uterine fibroid, complex hereditary spastic paraplegia
Unreviewed: Adenosine Deaminase Deficiency, Anxiety Disorder, Astrocytoma, Attention Deficit Hyperactivity Disorder, Bipolar Disorder, Breast Cancer, Breast Carcinoma, Breast neoplasm, Carcinoma, Cardiovascular Diseases, Cervical Cancer, Cervical Tumor, Cervix carcinoma, Combined molybdoflavoprotein enzyme deficiency, Congestive Heart Failure, Corpus callosum agenesis, Cystic Fibrosis, Development Disorder, Developmental Delay, Diabetes Mellitus, Dysplastic corpus callosum, Erectile Dysfunction, Galactosialidosis, Gilbert Disease, Gingivitis, Glioblastoma, Heart Failure, Hematologic neoplasm, Hematologic Neoplasms, Hemolytic Uremic Syndrome, Hemophilia, Huntington Disease, Hyperglycemia, Hyperkinesia, Hypoplasia Of Corpus Callosum, Immunologic Deficiency Syndromes, Leprechaunism syndrome, Leukemia, Liver carcinoma, Liver Cirrhosis, Liver failure, Lung Cancer, Lung carcinoma, Lung Neoplasms, Lymphoblastic Leukemia, Lymphocytic Leukemia, Lymphoid leukemia, Malignant Neoplasm, Melanoma, Mental Depression, Mental retardation, Motor delay, Moyamoya disease, Myeloblastic Leukemia, Myeloid leukemia, Myopia, Nasopharyngeal Carcinoma, Neoplasms, Nervous System Disorder, Neuroblastoma, Nystagmus, Optic Atrophy, Osteosarcoma, Paraplegia, Pendular nystagmus, Phosphoribosylpyrophosphate Synthetase Superactivity, Prostatic neoplasm, Pulmonary arterial hypertension, Retinal Dystrophy, Retinitis Pigmentosa, Retinoblastoma, Severe combined immunodeficiency disease, Spastic Paraplegia, Tarsal-Carpal Coalition Syndrome, Tendinopathy
|