Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
All A B C D E F G H I J K L M N O P Q R S T U V W X Y Z
8631 to 8640 of 15380 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

8631
Neuroglobin
-
Conotruncal cardiac defect

8632
Neuronal guanine nucleotide exchange factor
ARHGEF27, EPHEXIN
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Major depressive disorder, Obsessive-compulsive disorder, Parkinson disease, Schizophrenia, Tourette syndrome, Diabetes mellitus type 2

8633
Nerve growth factor
Beta-NGF, HSAN5, NGFB
Amnesia, Asthma, Bipolar disorder, Bronchial hyperreactivity, Charcot-marie-tooth disease, Skin ulcer, Congenital pain insensitivity, Congenital sensory neuropathy, Corneal ulcer, Cystitis, Degenerative disorder, Bipolar depression, Major depressive disorder, Tonic-clonic epilepsy, Glomerulonephritis
View all (21 more)

8634
Nerve growth factor receptor
CD271, Gp80-LNGFR, TNFRSF16, p75(NTR), p75NTR
Alzheimer disease, Bipolar disorder, Degenerative disorder, Major depressive disorder, Keratoconus, Melanoma, Neurodegenerative disorder, Prostatic neoplasms, Schizophrenia, Seizures

8635
N-glycanase 1
CDDG, CDG1V, PNG-1, PNG1, PNGase
Congenital disorder of deglycosylation, Global developmental delay, Intellectual developmental disorder, Peripheral neuropathy

8636
Neugrin, neurite outgrowth associated
DSC92
Color vision deficiency

8637
Non-homologous end joining factor 1
IMD124, MCOPCB13, XLF
Duodenal ulcer, Immunodeficiency, Microphthalmia, Osteoarthritis, Peptic ulcer disease, Severe combined immunodeficiency, Syndactyly

8638
NHERF family PDZ scaffold protein 1
EBP50, NHE-RF, NHERF, NHERF-1, NPHLOP2, SLC9A3R1
Ductal carcinoma of breast, Kidney disease, Dominant hypophosphatemia with nephrolithiasis and/or osteoporosis, Dominant hypophosphatemia with nephrolithiasis or osteoporosis, Nephrolithiasis

8639
NHERF family PDZ scaffold protein 2
E3KARP, NHE3RF2, NHERF-2, OCTS2, SIP-1, SIP1, SLC9A3R2, TKA-1
Cardiovascular disease, Hypertension, Metabolic syndrome, Open angle glaucoma, Diabetes mellitus type 2

8640
Nescient helix-loop-helix 1
HEN1, NSCL, NSCL1, bHLHa35
Alzheimer disease, Color vision deficiency, Gastroesophageal reflux disease, Schizophrenia