551
|
|
|
Neurexin 2 |
- |
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 |
552
|
|
|
Neurexin 3 |
C14orf60 |
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 2View all (20 more) |
553
|
|
|
NSA2 ribosome biogenesis factor |
CDK105, HCL-G1, HCLG1, HUSSY-29, HUSSY29, TINP1 |
|
554
|
|
|
Nuclear receptor binding SET domain protein 1 |
ARA267, KMT3B, SOTOS, SOTOS1, STO |
Asthma, Autism, Beckwith-wiedemann syndrome, Adenoid cystic carcinoma, Cholecystolithiasis, Deletion 5q35 syndrome, Desbuquois syndrome, Global developmental delay, Gout, Gross motor development delay, Holoprosencephaly, Non-immune hydrops fetalis, Intellectual developmental disorder, Microcephaly, Migraine, Neurodevelopmental disorder, Osteoarthritis, Osteopenia, Prostate cancer, Scoliosis, Sotos syndrome, Spastic paraplegia, Tetralogy of fallot, Diabetes mellitus type 2, Weaver syndromeView all (10 more) |
555
|
|
|
Nuclear receptor binding SET domain protein 2 |
KMT3F, KMT3G, MMSET, RAUST, REIIBP, TRX5, WHS, WHSC1 |
Anemia, Breast neoplasms, Congenital clubfoot, Congenital retrognathism, Desbuquois syndrome, Global developmental delay, Hypertrophic cardiomyopathy, Hypoglycemia, Neurodevelopmental disorder, Thrombocytopenia, Ventricular septal defect, Wolf-hirschhorn syndrome |
556
|
|
|
Nuclear receptor binding SET domain protein 3 |
KMT3F, KMT3G, WHISTLE, WHSC1L1, pp14328 |
|
557
|
|
|
NAD(P) dependent 3-beta-hydroxysteroid dehydrogenase NSDHL |
H105E3, SDR31E1, XAP104 |
Arachnodactyly, Byzanthine arch palate, Ck syndrome, Congenital hemidysplasia with ichthyosiform erythroderma and limb defects, Connective tissue disease, Desbuquois syndrome, Hearing impairment, Mitral valve prolapse, Perisylvian polymicrogyria, Scoliosis, Squamous cell carcinoma, Polymicrogyria |
558
|
|
|
N-ethylmaleimide sensitive factor, vesicle fusing ATPase |
DEE96, SEC18, SKD2 |
Alzheimer disease, Androgenetic alopecia, Breast cancer, Cancer, Colorectal cancer, Coronary artery disease, Developmental and epileptic encephalopathy, Estrogen-receptor negative breast cancer, Hypertension, Hypertrophic cardiomyopathy, Lung cancer, Major depressive disorder, Ovarian epithelial cancer, Migraine, Neurotic disorder, Obstructive sleep apnea syndrome, Ovarian cancer, Ovarian serous carcinoma, Parkinson disease, Peptic ulcer disease, Prostate cancer, Squamous cell carcinoma, Systemic lupus erythematosusView all (8 more) |
559
|
|
|
NSFL1 cofactor |
P47, UBX1, UBXD10, UBXN2C, dJ776F14.1 |
|
560
|
|
|
Neuronal vesicle trafficking associated 2 |
CALY3, HMP19 |
|
