EcoDrugPlus

Arachidonate 12-Lipoxygenase, 12s Type

Ensembl ID : ENSFCAG00000001355
Gene Symbol: ALOX12
5 Cross references
200 Possible Orthologues:

Arachidonate 5-Lipoxygenase

Ensembl ID : ENSFCAG00000013124
Gene Symbol: ALOX5
5 Cross references
222 Possible Orthologues:

Arachidonate 5-Lipoxygenase Activating Protein

Ensembl ID : ENSFCAG00000037195
Gene Symbol: ALOX5AP
5 Cross references
201 Possible Orthologues:

Arginine Vasopressin Receptor 1a

Ensembl ID : ENSFCAG00000014363
Gene Symbol: AVPR1A
5 Cross references
268 Possible Orthologues:

Arginine Vasopressin Receptor 1b

Ensembl ID : ENSFCAG00000006732
Gene Symbol: AVPR1B
5 Cross references
136 Possible Orthologues:

Arginine Vasopressin Receptor 2

Ensembl ID : ENSFCAG00000011384
Gene Symbol: AVPR2
5 Cross references
251 Possible Orthologues:

Aryl Hydrocarbon Receptor

Ensembl ID : ENSFCAG00000005018
Gene Symbol: AHR
5 Cross references
155 Possible Orthologues:

Aurora Kinase A

Ensembl ID : ENSFCAG00000024493
Gene Symbol: AURKA
5 Cross references
233 Possible Orthologues:

Aurora Kinase B

Ensembl ID : ENSFCAG00000028312
Gene Symbol: AURKB
5 Cross references
205 Possible Orthologues:

Aurora Kinase C

Ensembl ID : ENSFCAG00000002481
Gene Symbol: AURKC
5 Cross references
99 Possible Orthologues:

Beta-Secretase 1

Ensembl ID : ENSFCAG00000000178
Gene Symbol: BACE1
5 Cross references
220 Possible Orthologues:

Bradykinin Receptor B2

Ensembl ID : ENSFCAG00000006777
Gene Symbol: BDKRB2
5 Cross references
362 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).