Genesⓘ

Dataset:
? Reviewed gene-disease associations only.
? Curated and unreviewed gene-disease associations.
All ABCDEFGHIJKLMNOPQRSTUVWXYZ
Showing genes starting with "N"
321 to 330 of 533 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

321
Neurotrophic receptor tyrosine kinase 1
MTC, TRK, TRK1, TRKA, Trk-A, p140-TrkA
Alzheimer disease, Autoimmune disease, Bipolar disorder, Charcot-marie-tooth disease, Bipolar depression, Differentiated thyroid carcinoma, Glioma, Hereditary sensory and autonomic neuropathy, Hypothyroidism, Intellectual developmental disorder, Lewy body disease, Neuroblastoma, Neurodevelopmental disorders, Premature ovarian failure, Parkinson disease
View all (4 more)

322
Neurotrophic receptor tyrosine kinase 2
DEE58, EIEE58, GP145-TrkB, OBHD, TRKB, trk-B
Alzheimer disease, Androgenetic alopecia, Anxiety disorder, Astrocytoma, Autism, Bipolar disorder, Ischemic stroke, Colorectal cancer, Bipolar depression, Major depressive disorder, Developmental and epileptic encephalopathy, Developmental disability, Diabetic retinopathy, Glioma, Gout
View all (17 more)

323
Neurotrophic receptor tyrosine kinase 3
GP145-TrkC, TRKC, gp145(trkC)
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Central nervous system cancer, Congenital heart disease, Dementia, Differentiated thyroid carcinoma, Endometriosis, Gaucher disease, Glioblastoma, Glioma, Hypertrophic cardiomyopathy, Internet addiction disorder, Myeloid leukemia
View all (8 more)

324
Neurotensin
NMN-125, NN, NT, NT/N, NTS1
Astrocytoma, Bradycardia, Catalepsy, Major depressive disorder, Hyperkinesia, Lewy body disease, Depression, Mood disorder, Schizophrenia, Small vessel stroke

325
Neurotensin receptor 1
NTR
Alzheimer disease, Autism, Mood disorder, Schizophrenia

326
Nucleobindin 1
CALNUC, NUC
Oligodendroglioma, Stevens-johnson syndrome

327
Nucleobindin 2
HEL-S-109, NEFA
Crohn disease, Diabetes mellitus, Hypertension, Inflammatory bowel disease, Insomnia, Prostatic neoplasm, Schizophrenia, Skin disease, Diabetes mellitus, type 2, Ulcerative colitis

328
Nuclear mitotic apparatus protein 1
NMP-22, NUMA
Alzheimer disease, Deafness, Allergic contact dermatitis, Diabetic ketoacidosis, Diabetes mellitus, type 1

329
Nucleoporin 88
FADS4
Fetal akinesia deformation sequence, Human immunodeficiency virus infection, Metabolic syndrome, Pena-shokeir syndrome type i, Rheumatoid arthritis, Diabetes mellitus, type 2

330
Nucleoporin 98 and 96 precursor
ADIR2, NUP196, NUP96, Nup98-96
Anemia, Hematologic disease, Hirschsprung disease, Myeloid leukemia, Neutropenia, Obesity