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
8801 to 8810 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8801
NPC1 like intracellular cholesterol transporter 1
LDLCQ7, NPC11L1, SLC65A2
Cardiovascular disease, Hyperlipidemia, Metabolic syndrome, Schizophrenia

8802
NPC intracellular cholesterol transporter 2
EDDM1, HE1
Brain atrophy, Global developmental delay, Metabolic syndrome, Niemann-pick disease, Open angle glaucoma, Diabetes mellitus type 2, Upper aerodigestive tract neoplasm

8803
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

8804
Neuropeptide FF receptor 1
GPR147, NPFF1, NPFF1R1, OT7T022
Lymphoblastic leukemia, Squamous cell carcinoma

8805
Neuropeptide FF receptor 2
GPR74, HLWAR77, NPFF2, NPGPR
Central nervous system cancer, Gallbladder neoplasms, Glioblastoma, Glioma, Major depressive disorder

8806
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

8807
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

8808
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

8809
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

8810
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