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
8991 to 9000 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8991
Nucleoporin 62
IBSN, SNDI, p62
Biliary cirrhosis, Hearing loss, Leigh syndrome, Biliary cholangitis

8992
Nucleoporin 62 C-terminal like
-
Pancreatitis

8993
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

8994
Nucleoporin 88
FADS4
Fetal akinesia deformation sequence, Metabolic syndrome, Pena-shokeir syndrome , Rheumatoid arthritis, Diabetes mellitus type 2

8995
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

8996
Nucleoporin 98 and 96 precursor
ADIR2, NUP196, NUP96, Nup98-96
Anemia, Hematologic disease, Hirschsprung disease, Myeloid leukemia, Neutropenia, Obesity

8997
Nuclear protein 1, transcriptional regulator
COM1, P8
Crohn disease, Heart failure, Inflammatory bowel disease, Lipidoses, Lipoidosis, Pancreatitis, Diabetes mellitus type 1, Diabetes mellitus type 2, Ulcerative colitis

8998
Nuclear protein 2, transcriptional regulator
NUPR1L, P8
Developmental disorder

8999
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

9000
Nucleolar and spindle associated protein 1
ANKT, BM037, LNP, NUSAP, PRO0310p1, Q0310, SAPL
Hepatocellular carcinoma, Colorectal neoplasms, Microcephaly