Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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Showing genes starting with "N"
591 to 600 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

591
N-terminal Xaa-Pro-Lys N-methyltransferase 1
AD-003, C9orf32, HOMT1A, METTL11A, NRMT, NRMT1, NTM1A
Oligodendroglioma

592
N-terminal Xaa-Pro-Lys N-methyltransferase 2
C1orf184, HOMT1B, METTL11B, NTM1B
Atrial fibrillation, Venous thromboembolism

593
Netrin 1
MRMV4, NET1, NTN1L
Atypical femoral fracture, Brain edema, Breast cancer, Central nervous system cancer, Color vision deficiency, Congenital mirror movements, Glioblastoma, Glioma, Graves disease, Mirror movements, Neurotic disorder, Oligodendroglioma, Orofacial cleft

594
Netrin 4
PRO3091
Contact dermatitis, Gastroesophageal reflux disease, Gout, Kidney cancer, Pelvic organ prolapse, Psychiatric disorders

595
Netrin 5
-
Breast cancer

596
Netrin G1
Lmnt1, NetG1, NetrinG1
Anorexia nervosa, Rett syndrome, Bipolar disorder, Colorectal neoplasms, Neurodevelopmental disorder, Bipolar depression, Eating disorder, Leprosy, Metabolic syndrome, Kawasaki disease, Non-specific syndromic intellectual disability, Obesity, Osteonecrosis, Schizophrenia, Diabetes mellitus type 2

597
Netrin G2
LHLL9381, Lmnt2, NEDBASH, NTNG1, NetrinG2, bA479K20.1
Bell's palsy, Bipolar disorder, Color vision deficiency, Congenital neurologic anomalies, Bipolar depression, Global developmental delay, Gout, Intellectual developmental disorder seizures speech, Neurodevelopmental disorder, Non-specific syndromic intellectual disability, Schizophrenia, Systemic lupus erythematosus

598
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 disorder, Premature ovarian failure, Parkinson disease
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599
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, Dysthymic disorder, Early-onset obesity-hyperphagia-severe developmental delay syndrome
View all (18 more)

600
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, Congenital mesoblastic nephroma, Dementia, Differentiated thyroid carcinoma, Endometriosis, Gaucher disease, Glioblastoma, Glioma, Hypertrophic cardiomyopathy, Internet addiction disorder
View all (9 more)