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"
461 to 470 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

461
Aminopeptidase puromycin sensitive
AAP-S, MP100, PSA
Amyotrophic lateral sclerosis, Ankylosing spondylitis, Crohn disease, Dental caries, Glaucoma, Multiple sclerosis, Open angle glaucoma, Prostate cancer, Psoriasis, Sclerosing cholangitis, Ulcerative colitis

462
Neuropeptide FF receptor 1
GPR147, NPFF1, NPFF1R1, OT7T022
Lymphoblastic leukemia, Squamous cell carcinoma

463
Neuropeptide FF receptor 2
GPR74, HLWAR77, NPFF2, NPGPR
Central nervous system cancer, Gallbladder neoplasms, Glioblastoma, Glioma, Major depressive disorder

464
Nephrocystin 1
JBTS4, NPH1, SLSN1
Appendicitis, Bardet-biedl syndrome, Congenital anomalies of the kidney and urinary tract, Aplasia of the vermis, Joubert syndrome, Nephronophthisis, Kidney disease, Leber congenital amaurosis, Neurotic disorder, Retinitis pigmentosa, Senior-loken syndrome

465
Nephrocystin 3
CFAP31, MKS7, NPH3, RHPD, RHPD1, SLSN3
Anhydramnios, Hemolytic uremic syndrome, Polycystic kidney disease, Bardet-biedl syndrome, Aplasia of the vermis, Hypertension, Joubert syndrome, Kidney disease, Leber congenital amaurosis, Meckel-gruber syndrome, Nephronophthisis, Optic atrophy, Retinitis pigmentosa, Senior-loken syndrome

466
Nephrocystin 4
POC10, SLSN4
Alzheimer disease, Bardet-biedl syndrome, Behcet disease, Congenital anomalies of the kidney and urinary tract, Cholelithiasis, Kidney disease, Congenital heart disease, Joubert syndrome, Juvenile idiopathic arthritis, Nephronophthisis, Leber congenital amaurosis, Optic atrophy, Retinitis pigmentosa, Senior-loken syndrome

467
NPHS1 adhesion molecule, nephrin
CNF, NPHN, nephrin
Congenital nephrotic syndrome, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Glomerulonephritis, Hereditary steroid-resistant nephrotic syndrome, Hyperhomocysteinemia, Kidney disease, Nephrotic syndrome, Oligodendroglioma, Proteinuria, Steroid-resistant nephrotic syndrome

468
NPHS2 stomatin family member, podocin
PDCN, SRN1
Kidney disease, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Gout, Hereditary steroid-resistant nephrotic syndrome, Nephrotic syndrome, Nephrotic syndrome, idiopathic, steroid-resistant, Nephrotic syndrome, steroid-resistant, autosomal recessive, Steroid-resistant nephrotic syndrome

469
Nuclear pore complex interacting protein family member A5
NPIP
Mobius syndrome

470
Nuclear pore complex interacting protein family member B2
-
Gastric cancer