Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8591 to 8600 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8591
Neuralized E3 ubiquitin protein ligase 4
-
Autoimmune disease, Systemic lupus erythematosus, Diabetes mellitus type 1, Diabetes mellitus type 2

8592
Neuronal differentiation 1
BETA2, BHF-1, MODY6, NEUROD, T2D, bHLHa3
Neurodevelopmental disorder, Diabetes mellitus type 1, Diabetes mellitus type 2, Gallbladder neoplasms, Hyperglycemia, Maturity-onset diabetes of the young (mody), Maturity-onset diabetes of the young, Nervous system disease, Non-specific syndromic intellectual disability, Permanent neonatal diabetes mellitus, Retinitis pigmentosa

8593
Neuronal differentiation 2
DEE72, EIEE72, NDRF, bHLHa1
Asthma, Cardiovascular disease, Developmental and epileptic encephalopathy, Diabetes mellitus, Diabetic neuropathy, Dyslexia, Alzheimer disease, Hyperopia, Metabolic syndrome, Polycystic ovary syndrome, Rheumatoid arthritis, Schizophrenia, Diabetes mellitus type 2

8594
Neuronal differentiation 6
Atoh2, MATH2, Math-2, NEX1M, Nex1, bHLHa2
Alzheimer disease, Attention deficit hyperactivity disorder, Dementia, Major depressive disorder, Substance abuse

8595
Neurogenin 1
AKA, CCDDRD, Math4C, NEUROD3, bHLHa6, ngn1
Congenital cranial dysinnervation disorder, Schizoaffective disorder, Schizophrenia

8596
Neurogenin 3
Atoh5, Math4B, NGN-3, bHLHa7, ngn3
Atherosclerosis, Congenital malabsorptive diarrhea, Diabetes mellitus type 2, Permanent neonatal diabetes mellitus, Congenital malabsorptive diarrhea with diabetes mellitus and combined pituitary hormone deficiency

8597
Neurite extension and migration factor
KIAA2022, KIDLIA, MRX98, XLID98, XPN
Epilepsy, Epilepsy with myoclonic atonic seizures, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Neurodevelopmental disorder, X-linked intellectual disability, X-linked complex neurodevelopmental disorder

8598
Nexilin F-actin binding protein
CDM2M, CMH20, NELIN
Arrhythmogenic right ventricular cardiomyopathy, Cardiomyopathy, Dilated cardiomyopathy, Heart failure, Hypertrophic cardiomyopathy, Left ventricular disease, Left ventricular noncompaction cardiomyopathy, Long qt syndrome

8599
Neurofibromin 1
NFNS, VRNF, WSS
17q11 microdeletion syndrome, 17q11.2 microduplication syndrome, Astrocytoma, Autism, Autoimmune musculoskeletal system disorder, Bardet-biedl syndrome, Cafe-au-lait spots, Cervical lymphadenopathy, Desbuquois syndrome, Digestive system disease, Diverticular disease, Embryonal nuclear cataract, Endometrial cancer, Endometrial neoplasms, Febrile convulsion
View all (28 more)

8600
NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor
ACN, BANF, SCH, SWNV, merlin-1
Breast cancer, Renal cell carcinoma, Colorectal adenoma, Meningioma, Mesothelioma, Neurofibromatosis, Schwannomatosis