Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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10131 to 10140 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10131
RNA polymerase III subunit F
C34, IMD101, RPC39, RPC6
Immunodeficiency

10132
RNA polymerase III subunit G
C31, RPC32, RPC7
Autism

10133
RNA polymerase III subunit H
C25, RPC22.9, RPC8
46,xy gonadal dysgenesis, Gonadal dysgenesis, Mitochondrial disease, Optic atrophy

10134
RNA polymerase III subunit K
C11, C11-RNP3, HLD21, My010, RPC10, RPC11, RPC12.5
Hypomyelinating leukodystrophy, Stomach neoplasms

10135
RNA polymerase mitochondrial
APOLMT, COXPD55, MTRNAP, MTRPOL, h-mtRPOL
Progressive external ophthalmoplegia, Combined oxidative phosphorylation deficiency, Neurodevelopmental disorder

10136
POM121 transmembrane nucleoporin
P145, POM121A
Gout

10137
POM121 transmembrane nucleoporin C
POM121-2
Atrial fibrillation, Hypertension, Heart failure, Metabolic syndrome, Obesity, Osteoarthritis, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 2

10138
POM121 transmembrane nucleoporin like 12
-
Attention deficit hyperactivity disorder, Color vision deficiency, Tourette syndrome, Pelvic organ prolapse, Psoriasis, Substance abuse

10139
POM121 transmembrane nucleoporin like 2
POM121-L, POM121L
Angioedema, Asthma, Attention deficit hyperactivity disorder, Autism, Breast cancer, Obstructive pulmonary disease, Inflammatory bowel disease, Insomnia, Lung cancer, Major depressive disorder, Neurotic disorder, Psoriasis, Rheumatoid arthritis, Schizophrenia, Diabetes mellitus type 1

10140
Proopiomelanocortin
ACTH, CLIP, LPH, MSH, NPP, OBAIRH, POC
Amnesia, Aortic stenosis, Gouty arthritis, Autism, Bipolar disorder, Body weight, Bradycardia, Calcinosis, Renal cell carcinoma, Cardiomegaly, Cardiomyopathy, Catalepsy, Cerebral hemorrhage, Cerebral palsy, Cholelithiasis
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