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"
651 to 660 of 682 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

651
Nucleoporin 62 C-terminal like
-
Pancreatitis

652
Nucleoporin 85
FROUNT, NPHS17, Nup75
Alzheimer disease, Idiopathic steroid-resistant nephrotic syndrome, Genetic steroid-resistant nephrotic syndrome, Tourette syndrome, Hereditary steroid-resistant nephrotic syndrome, Nephrotic syndrome, Peripheral arterial disease, Seckel syndrome, Systemic sclerosis, Diabetes mellitus type 2

653
Nucleoporin 88
FADS4
Fetal akinesia deformation sequence, Metabolic syndrome, Pena-shokeir syndrome , Rheumatoid arthritis, Diabetes mellitus type 2

654
Nucleoporin 93
NIC96
Duchenne muscular dystrophy, Idiopathic steroid-resistant nephrotic syndrome, Focal glomerulosclerosis, Genetic steroid-resistant nephrotic syndrome, Hereditary steroid-resistant nephrotic syndrome, Nephrotic syndrome, Metabolic syndrome, Nephrotic syndrome, idiopathic, steroid-resistant, Diabetes mellitus type 2

655
Nucleoporin 98 and 96 precursor
ADIR2, NUP196, NUP96, Nup98-96
Anemia, Hematologic disease, Hirschsprung disease, Myeloid leukemia, Neutropenia, Obesity

656
Nuclear protein 1, transcriptional regulator
COM1, P8
Crohn disease, Heart failure, Inflammatory bowel disease, Leprosy, Lipidoses, Lipoidosis, Liver cirrhosis, Pancreatitis, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis

657
Nuclear protein 2, transcriptional regulator
NUPR1L, P8
Disorder of development or morphogenesis

658
NUS1 dehydrodolichyl diphosphate synthase subunit
C6orf68, CDG1AA, MGC:7199, MRD55, NgBR, TANGO14
Bladder exstrophy, Congenital disorder of glycosylation, Coronary artery disease, Diabetes mellitus type 2, Fatty liver, Fatty liver, alcoholic, Hyperglycemia, Intellectual developmental disorder, Melanoma, Metabolic syndrome, Developmental and epileptic encephalopathy, Perisylvian syndrome, Progressive myoclonic epilepsy, Schizophrenia

659
Nucleolar and spindle associated protein 1
ANKT, BM037, LNP, NUSAP, PRO0310p1, Q0310, SAPL
Hepatocellular carcinoma, Colorectal neoplasms, Microcephaly

660
Nuclear transport factor 2
NTF-2, NTF2, PP15
Alzheimer disease