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
10121 to 10130 of 15380 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

10121
RNA polymerase II subunit B
POL2RB, RPB2, hRPB140
Breast cancer, Congenital heart disease

10122
RNA polymerase II subunit D
HSRBP4, HSRPB4, RBP4, RPB16, RPB4
Alzheimer disease

10123
RNA polymerase II, I and III subunit E
RPABC1, RPB5, XAP4, hRPB25, hsRPB5
Alzheimer disease, Autism, Small vessel stroke

10124
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

10125
RNA polymerase II subunit J
POLR2J1, RPB11, RPB11A, RPB11m, hRPB14
Breast cancer

10126
RNA polymerase II, I and III subunit K
ABC10-alpha, RPABC4, RPB10alpha, RPB12, RPB7.0, hRPB7.0, hsRPB10a
Interstitial lung disease

10127
RNA polymerase II subunit M
GCOM1, GRINL1A, Gdown, Gdown1
Asthma, Atrial fibrillation, Hypertension, Osteoarthritis

10128
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

10129
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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10130
RNA polymerase III subunit C
C82, RPC3, RPC62
Gout