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"
551 to 560 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

551
Neurturin
NTN
Alzheimer disease, Hirschsprung disease

552
Neurexin 1
Hs.22998, PTHSL2, SCZD17
Alzheimer disease, Attention deficit hyperactivity disorder, Autism, Biliary tract cancer, Bipolar disorder, Central nervous system cancer, Cervical cancer, Chromosome 2p16.3 deletion syndrome, Color vision deficiency, Neurodevelopmental disorder, Coronary artery disease, Craniofacial abnormalities, Dementia, Major depressive disorder, Dry eye syndrome
View all (22 more)

553
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

554
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
View all (20 more)

555
NSA2 ribosome biogenesis factor
CDK105, HCL-G1, HCLG1, HUSSY-29, HUSSY29, TINP1
Biliary cirrhosis, Liver cirrhosis, Biliary cholangitis

556
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
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557
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

558
Nuclear receptor binding SET domain protein 3
KMT3F, KMT3G, WHISTLE, WHSC1L1, pp14328
Attention deficit hyperactivity disorder, Obesity, Obsessive-compulsive disorder, Schizophrenia, Tourette syndrome

559
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

560
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
View all (8 more)