EcoDrugPlus

Alcohol Dehydrogenase 5 (Class Iii), Chi Polypeptide

Ensembl ID : ENSLLEG00000010302
Gene Symbol: ADH5
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406 Possible Orthologues:


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Amine Oxidase Copper Containing 1

Ensembl ID : ENSLLEG00000014751
Gene Symbol: AOC1
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231 Possible Orthologues:


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Amyloid Beta Precursor Protein

Ensembl ID : ENSLLEG00000008369
Gene Symbol: APP
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276 Possible Orthologues:


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Androgen Receptor

Ensembl ID : ENSLLEG00000020805
Gene Symbol: AR
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277 Possible Orthologues:


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Angiotensin Ii Receptor Type 1

Ensembl ID : ENSLLEG00000007088
Gene Symbol: AGTR1
1 View Cross-references
207 Possible Orthologues:


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Aph-1 Homolog A, Gamma-Secretase Subunit

Ensembl ID : ENSLLEG00000023550
Gene Symbol: APH1A
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137 Possible Orthologues:


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Arachidonate 5-Lipoxygenase

Ensembl ID : ENSLLEG00000025304
Gene Symbol: ALOX5
1 View Cross-references
220 Possible Orthologues:


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Arachidonate 5-Lipoxygenase Activating Protein

Ensembl ID : ENSLLEG00000021787
Gene Symbol: ALOX5AP
1 View Cross-references
200 Possible Orthologues:


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Arginine Vasopressin Receptor 1a

Ensembl ID : ENSLLEG00000017308
Gene Symbol: AVPR1A
1 View Cross-references
264 Possible Orthologues:


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Arginine Vasopressin Receptor 1b

Ensembl ID : ENSLLEG00000010254
Gene Symbol: AVPR1B
1 View Cross-references
135 Possible Orthologues:


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Arginine Vasopressin Receptor 2

Ensembl ID : ENSLLEG00000026789
Gene Symbol: AVPR2
1 View Cross-references
231 Possible Orthologues:


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Aryl Hydrocarbon Receptor

Ensembl ID : ENSLLEG00000017103
Gene Symbol: AHR
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154 Possible Orthologues:


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PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).