EcoDrugPlus

Catechol-O-Methyltransferase

Ensembl ID : ENSSTOG00000027573
Gene Symbol: COMT
3 Cross references
275 Possible Orthologues:

Cathepsin K

Ensembl ID : ENSSTOG00000013868
Gene Symbol: CTSK
3 Cross references
240 Possible Orthologues:

Cathepsin S

Ensembl ID : ENSSTOG00000021432
Gene Symbol: CTSS
3 Cross references
269 Possible Orthologues:

Cell Division Cycle 7

Ensembl ID : ENSSTOG00000002130
Gene Symbol: CDC7
3 Cross references
208 Possible Orthologues:

Checkpoint Kinase 1

Ensembl ID : ENSSTOG00000002463
Gene Symbol: CHEK1
3 Cross references
177 Possible Orthologues:

Checkpoint Kinase 2

Ensembl ID : ENSSTOG00000011573
Gene Symbol: CHEK2
4 Cross references
204 Possible Orthologues:

Cholecystokinin A Receptor

Ensembl ID : ENSSTOG00000028796
Gene Symbol: CCKAR
4 Cross references
200 Possible Orthologues:

Cholecystokinin B Receptor

Ensembl ID : ENSSTOG00000011354
Gene Symbol: CCKBR
3 Cross references
264 Possible Orthologues:

Cholesteryl Ester Transfer Protein

Ensembl ID : ENSSTOG00000003544
Gene Symbol: CETP
4 Cross references
137 Possible Orthologues:

Cholinergic Receptor Muscarinic 1

Ensembl ID : ENSSTOG00000004514
Gene Symbol: CHRM1
3 Cross references
101 Possible Orthologues:

Cholinergic Receptor Muscarinic 2

Ensembl ID : ENSSTOG00000012061
Gene Symbol: CHRM2
3 Cross references
259 Possible Orthologues:

Cholinergic Receptor Muscarinic 3

Ensembl ID : ENSSTOG00000021752
Gene Symbol: CHRM3
3 Cross references
255 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).