Pharmaco-transcriptomicsUp/down regulation of genes due to the metabolism of pharmaceutical compounds

Pharmaco-genomics Pharmaco-metabolomics Pharmaco-transcriptomics Pharmaco-proteomics Search

Displaying entries 35201 - 35225 of 102031 in total

Drug	Drug Groups	Gene	Gene ID	Change	Interaction	Chromosome	References
							Clear
Diphencyprone	Investigational	SRXN1	140809	upregulated	diphenylcyclopropenone results in increased expression of SRXN1 mRNA	20p13	A22390
Diphencyprone	Investigational	STC2	8614	downregulated	diphenylcyclopropenone results in decreased expression of STC2 mRNA	5q35.2	A22390
Diphencyprone	Investigational	TXN	7295	upregulated	diphenylcyclopropenone results in increased expression of TXN mRNA	9q31.3	A20399
Dipyridamole	Approved Investigational	FADD	8772	upregulated	Dipyridamole results in increased expression of FADD mRNA	11q13.3	A20468
Dipyridamole	Approved Investigational	FOS	2353	upregulated	Dipyridamole results in increased expression of FOS mRNA	14q24.3	A20417
Disopyramide	Approved Investigational	ASAH1	427	upregulated	Disopyramide results in increased expression of ASAH1 mRNA	8p22	A20438
Disopyramide	Approved Investigational	NR0B2	8431	downregulated	Disopyramide results in decreased expression of NR0B2 mRNA	1p36.11	A20438
Disulfiram	Approved Investigational	AARS	16	upregulated	[Disulfiram binds to Copper] which results in increased expression of AARS mRNA	16q22.1	A21750
Disulfiram	Approved Investigational	ABCA1	19	upregulated	[Disulfiram binds to Copper] which results in increased expression of ABCA1 mRNA	9q31.1	A21750
Disulfiram	Approved Investigational	ABCA3	21	upregulated	[Disulfiram binds to Copper] which results in increased expression of ABCA3 mRNA	16p13.3	A21750
Disulfiram	Approved Investigational	ABCG1	9619	upregulated	[Disulfiram binds to Copper] which results in increased expression of ABCG1 mRNA	21q22.3	A21750
Disulfiram	Approved Investigational	ACAD11	84129	upregulated	[Disulfiram binds to Copper] which results in increased expression of ACAD11 mRNA	3q22.1	A21750
Disulfiram	Approved Investigational	ACSS2	55902	upregulated	[Disulfiram binds to Copper] which results in increased expression of ACSS2 mRNA	20q11.22	A21750
Disulfiram	Approved Investigational	ACTA2	59	upregulated	[Disulfiram binds to Copper] which results in increased expression of ACTA2 mRNA	10q23.31	A21750
Disulfiram	Approved Investigational	ADAM9	8754	upregulated	[Disulfiram binds to Copper] which results in increased expression of ADAM9 mRNA	8p11.22	A21750
Disulfiram	Approved Investigational	ADAMTS1	9510	downregulated	[Disulfiram binds to Copper] which results in decreased expression of ADAMTS1 mRNA	21q21.3	A21750
Disulfiram	Approved Investigational	ADARB1	104	upregulated	[Disulfiram binds to Copper] which results in increased expression of ADARB1 mRNA	21q22.3	A21750
Disulfiram	Approved Investigational	ADCY3	109	upregulated	[Disulfiram binds to Copper] which results in increased expression of ADCY3 mRNA	2p23.3	A21750
Disulfiram	Approved Investigational	ADGRE5	976	upregulated	[Disulfiram binds to Copper] which results in increased expression of ADGRE5 mRNA	19p13.12	A21750
Disulfiram	Approved Investigational	ADM	133	downregulated	[Disulfiram binds to Copper] which results in decreased expression of ADM mRNA	11p15.4	A21750
Disulfiram	Approved Investigational	AFAP1	60312	upregulated	[Disulfiram binds to Copper] which results in increased expression of AFAP1 mRNA	4p16.1	A21750
Disulfiram	Approved Investigational	AGXT	189	downregulated	[Disulfiram binds to Copper] which results in decreased expression of AGXT mRNA	2q37.3	A21750
Disulfiram	Approved Investigational	AHSA1	10598	downregulated	[Disulfiram binds to Copper] which results in decreased expression of AHSA1 mRNA	14q24.3	A21750
Disulfiram	Approved Investigational	AKR1B1	231	upregulated	Disulfiram results in increased expression of AKR1B1 mRNA	7q33	A21074
Disulfiram	Approved Investigational	AKR1B10	57016	upregulated	Disulfiram results in increased expression of AKR1B10 mRNA	7q33	A21074

Displaying entries 35201 - 35225 of 102031 in total

Pharmaco-transcriptomicsUp/down regulation of genes due to the metabolism of pharmaceutical compounds

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