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
Showing genes starting with "N"
571 to 580 of 682 Genes
Show
Entrez ID Gene Symbol Gene Name Synonyms Diseases

571
NOP2/Sun RNA methyltransferase 3
COXPD48, MST077, MSTP077
Anorexia nervosa, Asthma, Attention deficit hyperactivity disorder, Combined oxidative phosphorylation deficiency, Gastric cancer, Gout, Hyperuricemia, Kidney cancer, Major depressive disorder, Metabolic syndrome, Substance abuse, Diabetes mellitus type 2

572
NOP2/Sun RNA methyltransferase 4
SHTAP
Alzheimer disease, Bipolar disorder, Major depressive disorder, Prostate cancer, Schizophrenia

573
NOP2/Sun RNA methyltransferase 6
4933414E04Rik, ARL5B-AS1, MRT82, NOPD1
Breast neoplasms, Intellectual developmental disorder, Schizophrenia, Scoliosis

574
NOP2/Sun RNA methyltransferase family member 7
-
Male infertility, Psoriasis

575
5', 3'-nucleotidase, cytosolic
DNT, DNT1, HEL74, P5N2, PN-I, PN-II, UMPH2, cdN, dNT-1
Colorectal neoplasms

576
5'-nucleotidase, cytosolic IA
CN-I, CN-IA, CN1, CN1A, CNI
Amyotrophic lateral sclerosis, Lymphocytic leukemia, Metabolic syndrome, Myocardial infarction, Diabetes mellitus type 2

577
5'-nucleotidase, cytosolic IB
AIRP, CN-IB, CN1B
Atrial fibrillation, Bulimia, Corneal neovascularization, Coronary artery disease, Diverticular disease, Hypertension, Keratitis

578
NT5C1B-RDH14 readthrough
AIRP, NT5C1B, cN-IB, cN1B
Cerebellar atrophy, Corneal neovascularization, Intellectual developmental disorder, Keratitis

579
5'-nucleotidase, cytosolic II
GMP, NT5B, PNT5, SPG45, SPG65, cN-II
Anorexia nervosa, Attention deficit hyperactivity disorder, Autism, Spastic paraplegia, Barrett esophagus, Bipolar disorder, Brain aneurysm, Cannabis abuse, Cardiovascular disease, Hereditary spastic paraplegia, Coronary artery disease, Esophageal disease, Gout, Hypertension, Major depressive disorder
View all (13 more)

580
5'-nucleotidase, cytosolic IIIA
CNSHA8, NT5C3, P5'N-1, P5N-1, PN-I, POMP, PSN1, UMPH, UMPH1, cN-III, hUMP1, p36
Congenital nonspherocytic hemolytic anemia, Hemolytic anemia, Chloracne, Uridine monophosphate hydrolase deficiency