Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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8911 to 8920 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

8911
Nuclear speckle splicing regulatory protein 1
CCDC55, HSPC095, NEDSSBA, NSrp70
Obstructive pulmonary disease, Neurodevelopmental disorder

8912
NOP2/Sun RNA methyltransferase 2
MISU, MRT5, SAKI, TRM4
Autism, Nonsyndromic intellectual disability, Dubowitz syndrome, Intellectual developmental disorder, Hypertension

8913
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

8914
NOP2/Sun RNA methyltransferase 4
SHTAP
Alzheimer disease, Bipolar disorder, Major depressive disorder, Prostate cancer, Schizophrenia

8915
NOP2/Sun RNA methyltransferase 6
4933414E04Rik, ARL5B-AS1, MRT82, NOPD1
Breast neoplasms, Intellectual developmental disorder, Schizophrenia, Scoliosis

8916
NOP2/Sun RNA methyltransferase family member 7
-
Male infertility, Psoriasis

8917
5', 3'-nucleotidase, cytosolic
DNT, DNT1, HEL74, P5N2, PN-I, PN-II, UMPH2, cdN, dNT-1
Colorectal neoplasms

8918
5'-nucleotidase, cytosolic IA
CN-I, CN-IA, CN1, CN1A, CNI
Amyotrophic lateral sclerosis, Lymphocytic leukemia, Metabolic syndrome, Myocardial infarction, Diabetes mellitus type 2

8919
5'-nucleotidase, cytosolic IB
AIRP, CN-IB, CN1B
Atrial fibrillation, Bulimia, Corneal neovascularization, Coronary artery disease, Diverticular disease, Hypertension, Keratitis

8920
NT5C1B-RDH14 readthrough
AIRP, NT5C1B, cN-IB, cN1B
Cerebellar atrophy, Corneal neovascularization, Intellectual developmental disorder, Keratitis