981
|
|
|
Neuropeptide FF receptor 2 |
GPR74, HLWAR77, NPFF2, NPGPR |
Curated: Central nervous system cancer, Gallbladder neoplasms, Glioblastoma, Glioma, Major depressive disorder
Unreviewed: Coronary Arteriosclerosis, Coronary artery disease, Coronary Heart Disease, Lymphoma, Narcolepsy, Neuroblastoma, Obesity, Prostatic neoplasm
|
982
|
|
|
Nephrocystin 1 |
JBTS4, NPH1, SLSN1 |
Curated: 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, nephronophthisis 1
Unreviewed: Age-related macular degeneration, Agenesis Of Corpus Callosum, Alport Syndrome, Alzheimer disease, Anemia, Apraxia, Arteriosclerosis, Autism, Autoimmune Polyendocrinopathy, Bardet-Biedl Syndrome, Brain stem neoplasms, Cataract, Cerebellar vermis agenesis, Cholelithiasis, Ciliopathies, Ciliopathy, Congenital abnormalities, Congenital Cerebral Hernia, Congenital Coloboma Of Iris, Congenital Hepatic Fibrosis, Congenital Hypoplasia Of Penis, Cryptorchidism, Cystic Kidney Disease, Dandy-Walker Syndrome, Developmental Delay, Disorder Of Eye, Dwarfism, Glomerulosclerosis, Hairy cell leukemia, Hirschsprung Disease, Hydatidiform mole, Hydrocephalus, Hypertension, Hypogonadism, Hypoplasia of the ovary, Impaired Cognition, Intellectual developmental disorder, Jacobsen Syndrome, Johanson-Blizzard Syndrome, Joubert Syndrome With Renal Defect, Kidney Disease, Kidney Failure, Liver failure, Liver Fibrosis, Macular degeneration, Male infertility, Meckel Syndrome, Mental retardation, Multicystic renal dysplasia, Nephroblastoma, Nephrosis, Congenital, Nephrotic Syndrome, Normal pressure hydrocephalus, Nystagmus, Obesity, Oculomotor apraxia, Oculovestibuloauditory Syndrome, Polymicrogyria, Postaxial hand polydactyly, Premature Menopause, Ptosis, Renal corticomedullary cysts, Renal dysplasia and retinal aplasia, Renal glycosuria, Renal Insufficiency, Retinal Dystrophy, Retinitis Pigmentosa, Rod-cone dystrophy, Scoliosis, Senior-Loken Syndrome, Speech Disorders, Strabismus, Syndactyly of fingers, Visual disorder
|
983
|
|
|
Nephrocystin 3 |
CFAP31, MKS7, NPH3, RHPD, RHPD1, SLSN3 |
Curated: 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
Unreviewed: Aortic Valve Sclerosis, Asplenia, Atrial Septal Defect, Biliary cirrhosis, Carcinogenesis, Cataract, Cholestasis, Ciliopathies, Ciliopathy, Cirrhosis, Congenital anomalies of kidney and urinary tract, Congenital Heart Disease, Congenital Hepatic Fibrosis, Congenital malrotation of intestine, Cystic Kidney Disease, Dandy-Walker Syndrome, Developmental Delay, Disorder Of Eye, Drachtman Weinblatt Sitarz syndrome, Dwarfism, Fibrosis Of Pancreas, Heart valve disease, Hepatic fibrosis, Hydrocephalus, Idiopathic pulmonary fibrosis, Jaundice, Kidney Disease, Kidney Failure, Liver cirrhosis, Liver Cyst, Liver Fibrosis, Meckel syndrome, Meckel-Like Syndrome, Medullary Cystic Kidney Disease, Multicystic renal dysplasia, Pancreatic Cyst, Patent ductus arteriosus, Polydactyly, Polysplenia, Premature Menopause, Prostatic neoplasm, Pulmonary hypoplasia, Renal cell carcinoma, Renal corticomedullary cysts, Renal dysplasia, Renal dysplasia and retinal aplasia, Renal Glomerular Disease, Renal Insufficiency, RENAL-HEPATIC-PANCREATIC DYSPLASIA, Retinal Diseases, Retinal Dystrophy, Retinitis Pigmentosa, Senior-Loken Syndrome, Situs Inversus, Sjogren-Larsson Syndrome
|
984
|
|
|
NPHP3-ACAD11 readthrough (NMD candidate) |
NPHP3 |
Curated: N/A
Unreviewed: Ciliopathies, Congenital Torticollis, Cutis marmorata, Developmental Delay, Eczema, Epileptic encephalopathy, Esotropia, Exotropia, Horizontal nystagmus, Hypoplasia Of Corpus Callosum, Meckel syndrome, Nephronophthisis, Nystagmus, Oropharyngeal Dysphagia, Plagiocephaly, Polycystic kidney disease, Posteriorly Rotated Ear, RENAL-HEPATIC-PANCREATIC DYSPLASIA, Situs Inversus, Spasms X-Linked, Spinocerebellar Ataxia
|
985
|
|
|
NPHP3 antisense RNA 1 |
NCRNA00119 |
Curated: N/A
Unreviewed: Nephronophthisis
|
986
|
|
|
Nephrocystin 4 |
POC10, SLSN4 |
Curated: 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, nephronophthisis 4
Unreviewed: Anemia, Arima Syndrome, Cataract, Cerebellar vermis agenesis, Ciliopathies, Ciliopathy, Congenital heart defects, Congenital Hepatic Fibrosis, Conotruncal cardiac defect, Developmental Delay, Disorder Of Eye, Dwarfism, Focal segmental glomerulosclerosis, Glomerulosclerosis, Hydrocephalus, Hypertension, Kidney Disease, Kidney failure, Kidney neoplasm, Lung neoplasms, Male infertility, Premature Menopause, Renal corticomedullary cysts, Renal dysplasia and retinal aplasia, Retinal Dystrophy, Retinitis Pigmentosa, Rod-cone dystrophy, Rotary nystagmus, Senior-Loken Syndrome, Situs ambiguus
|
987
|
|
|
NPHS1 adhesion molecule, nephrin |
CNF, NPHN, nephrin |
Curated: 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
Unreviewed: Absence epilepsy, Bright Disease, Cataract, Chromosome 22q11.2 microduplication syndrome, Colon Carcinoma, Colonic Neoplasms, Congenital alveolar dysplasia, Diabetes, Diabetes Mellitus, Diabetes mellitus, type 2, Diabetic Nephropathy, Diabetic neuropathy, Diarrhea, Finnish Congenital Nephrotic Syndrome, Focal segmental glomerulosclerosis, Gastroesophageal Reflux Disease, Genetic Steroid-Resistant Nephrotic Syndrome, Glaucoma, Glomerular Hyalinosis, Glomerulosclerosis, Hyperglycemia, Hyperlipidemia, Hypertension, Hypoalbuminemia, Hypoproteinemia, Hypothyroidism, Iga nephropathy, Infective arthritis, Kidney Disease, Kidney Failure, Lipoid Nephrosis, Lupus nephritis, Macular corneal dystrophy, Medium Chain Acyl-CoA Dehydrogenase Deficiency, Membranous Glomerulonephritis, Mesangial sclerosis, Mitral Valve Stenosis, Multiple Sclerosis, Nephritis, Nephroblastoma, Nephrosis, Nephrosis, Congenital, Nephrotic Syndrome, Netherton syndrome, Neuronal Ceroid Lipofuscinosis, Obesity, Pierson Syndrome, Prostatitis, Renal Glomerular Disease, Renal Insufficiency, Septicemia, Steroid resistant nephrotic syndrome, Systemic lupus erythematosus
|
988
|
|
|
NPHS2 stomatin family member, podocin |
PDCN, SRN1 |
Curated: 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
Unreviewed: Alport Syndrome, Alport Syndrome, X-Linked, Amyloidosis, Arteriosclerosis, Atherosclerosis, Azoospermia, Cataract, Diabetes, Diabetes Mellitus, Diabetic Nephropathy, Diabetic neuropathy, Eclampsia, Edema, Fabry disease, Finnish Congenital Nephrotic Syndrome, Focal segmental glomerulosclerosis, Genetic Steroid-Resistant Nephrotic Syndrome, Glomerular Hyalinosis, Glomerulonephritis, Glomerulosclerosis, Hematuria, Hyperlipidemia, Hypertension, Hypertensive Nephropathy, Hypoalbuminemia, Iga nephropathy, Kidney Disease, Kidney Failure, Kidney neoplasm, Lipoid Nephrosis, Macular corneal dystrophy, Membranous Glomerulonephritis, Mesangial sclerosis, Metabolic Diseases, Multicystic renal dysplasia, Myocardial Ischemia, Nephritis, Nephroblastoma, Nephrosclerosis, Nephrosis, Nephrosis, Congenital, Nephrotic Syndrome, Netherton syndrome, Pierson Syndrome, Polycystic kidney disease, Proteinuria, Renal cell carcinoma, Renal fibrosis, Renal Glomerular Disease, Renal Insufficiency, Sarcoma, Steroid resistant nephrotic syndrome, Steroid-Sensitive Nephrotic Syndrome, Thin Basement Membrane Disease, Trichohepatoenteric Syndrome, Wilms tumor
|
989
|
|
|
Nuclear pore complex interacting protein family member A1 |
NPIP, NPIPA, morpheus |
Curated: N/A
Unreviewed: N/A
|
990
|
|
|
Nuclear pore complex interacting protein family member A2 |
NPIP, NPIPA1 |
Curated: N/A
Unreviewed: Congenital Exomphalos, Medullary thyroid cancer, Pseudoxanthoma elasticum
|