Genes | GeDiPNet - Gene Disease Pathway & Associations

Dataset:

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 1361 Genes

Show

	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
801	5434	POLR2E	RNA polymerase II, I and III subunit E	RPABC1, RPB5, XAP4, hRPB25, hsRPB5	Alzheimer disease, Autism, Small vessel stroke
802	5435	POLR2F	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
803	5439	POLR2J	RNA polymerase II subunit J	POLR2J1, RPB11, RPB11A, RPB11m, hRPB14	Breast cancer
804	5440	POLR2K	RNA polymerase II, I and III subunit K	ABC10-alpha, RPABC4, RPB10alpha, RPB12, RPB7.0, hRPB7.0, hsRPB10a	Interstitial lung disease
805	81488	POLR2M	RNA polymerase II subunit M	GCOM1, GRINL1A, Gdown, Gdown1	Asthma, Atrial fibrillation, Hypertension, Osteoarthritis
806	11128	POLR3A	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
807	55703	POLR3B	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 View all (1 more)
808	10623	POLR3C	RNA polymerase III subunit C	C82, RPC3, RPC62	Gout
809	10621	POLR3F	RNA polymerase III subunit F	C34, IMD101, RPC39, RPC6	Immunodeficiency
810	10622	POLR3G	RNA polymerase III subunit G	C31, RPC32, RPC7	Autism

«««...79 808182 83...»»»