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 "P"
811 to 820 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

811
RNA polymerase III subunit B
C128, CMT1I, HLD8, INMAP, RPC2
Alzheimer disease, Central nervous system cancer, Cerebellar ataxia, Charcot-marie-tooth disease, Dementia, Desbuquois syndrome, Glioblastoma, Glioma, Hypogonadotropic hypogonadism, Hypomyelinating leukodystrophy, Intellectual developmental disorder, Leukodystrophy, Neurodevelopmental disorder, Parkinson disease, Tourette syndrome
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812
RNA polymerase III subunit C
C82, RPC3, RPC62
Gout

813
RNA polymerase III subunit F
C34, IMD101, RPC39, RPC6
Immunodeficiency

814
RNA polymerase III subunit G
C31, RPC32, RPC7
Autism

815
RNA polymerase III subunit H
C25, RPC22.9, RPC8
46, xx gonadal dysgenesis, Gonadal dysgenesis, Mitochondrial disease, Optic atrophy

816
RNA polymerase III subunit K
C11, C11-RNP3, HLD21, My010, RPC10, RPC11, RPC12.5
Hypomyelinating leukodystrophy, Stomach neoplasms

817
RNA polymerase mitochondrial
APOLMT, COXPD55, MTRNAP, MTRPOL, h-mtRPOL
Progressive external ophthalmoplegia, Combined oxidative phosphorylation deficiency, Neurodevelopmental disorder

818
POM121 transmembrane nucleoporin
P145, POM121A
Gout

819
POM121 transmembrane nucleoporin C
POM121-2
Atrial fibrillation, Hypertension, Heart failure, Metabolic syndrome, Obesity, Osteoarthritis, Schizophrenia, Systemic lupus erythematosus, Diabetes mellitus type 2

820
POM121 transmembrane nucleoporin like 12
-
Attention deficit hyperactivity disorder, Color vision deficiency, Tourette syndrome, Pelvic organ prolapse, Psoriasis, Substance abuse