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 "P"
801 to 810 of 1369 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

801
RNA polymerase I subunit H
A12.2, HTEX-6, HTEX6, Rpa12, TCTEX6, TEX6, ZNRD1, ZR14, hZR14, tctex-6
Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Lung cancer, Major depressive disorder, Multiple sclerosis, Rheumatoid arthritis, Sarcoidosis, Schizophrenia, Squamous cell carcinoma, Stomach neoplasms, Upper aerodigestive tract neoplasm

802
RNA polymerase II subunit A
NEDHIB, POLR2, POLRA, RPB1, RPBh1, RPO2, RPOL2, RpIILS, hRPB220, hsRPB1
Atrial fibrillation, Cardioembolic stroke, Central nervous system cancer, Developmental disability, Endometriosis, Glioma, Hypertension, Migraine, Neurodevelopmental disorder, Osteoarthritis, Parkinson disease, Uterine fibroid

803
RNA polymerase II subunit B
POL2RB, RPB2, hRPB140
Breast cancer, Congenital heart disease

804
RNA polymerase II subunit D
HSRBP4, HSRPB4, RBP4, RPB16, RPB4
Alzheimer disease

805
RNA polymerase II, I and III subunit E
RPABC1, RPB5, XAP4, hRPB25, hsRPB5
Alzheimer disease, Autism, Small vessel stroke

806
RNA polymerase II, I and III subunit F
HRBP14.4, POLRF, RPABC14.4, RPABC2, RPB14.4, RPB6, RPC15
Charcot-marie-tooth disease, Hearing impairment, Hirschsprung disease, Intellectual developmental disorder, Kallmann syndrome, Waardenburg syndrome

807
RNA polymerase II subunit J
POLR2J1, RPB11, RPB11A, RPB11m, hRPB14
Breast cancer

808
RNA polymerase II, I and III subunit K
ABC10-alpha, RPABC4, RPB10alpha, RPB12, RPB7.0, hRPB7.0, hsRPB10a
Interstitial lung disease

809
RNA polymerase II subunit M
GCOM1, GRINL1A, Gdown, Gdown1
Asthma, Atrial fibrillation, Hypertension, Osteoarthritis

810
RNA polymerase III subunit A
ADDH, C160, HLD7, RPC1, RPC155, WDRTS, hRPC155
Bipolar disorder, Cerebellar ataxia, Desbuquois syndrome, Hypomyelinating leukodystrophy, Leukodystrophy, Movement disorder, Nonalcoholic fatty liver disease, Spastic ataxia, Tremor-ataxia-central hypomyelination syndrome, Wiedemann-rautenstrauch syndrome