EcoDrugPlus

Catechol-O-Methyltransferase

Ensembl ID : ENSAPOG00000012877
Gene Symbol: COMT
3 Cross references
215 Possible Orthologues:

Cathepsin C

Ensembl ID : ENSAPOG00000018782
Gene Symbol: CTSC
3 Cross references
239 Possible Orthologues:

Cathepsin K-Like

Ensembl ID : ENSAPOG00000015162
Gene Symbol: LOC110964438
3 Cross references
226 Possible Orthologues:

Cathepsin S

Ensembl ID : ENSAPOG00000017560
Gene Symbol: CTSS
3 Cross references
181 Possible Orthologues:

Cathepsin S-Like

Ensembl ID : ENSAPOG00000015157
Gene Symbol: LOC110964435
3 Cross references
235 Possible Orthologues:

Cell Division Cycle 7

Ensembl ID : ENSAPOG00000005122
Gene Symbol: CDC7
3 Cross references
209 Possible Orthologues:

Checkpoint Kinase 1

Ensembl ID : ENSAPOG00000013534
Gene Symbol: CHEK1
3 Cross references
179 Possible Orthologues:

Checkpoint Kinase 2

Ensembl ID : ENSAPOG00000006578
Gene Symbol: CHEK2
3 Cross references
206 Possible Orthologues:

Cholecystokinin A Receptor

Ensembl ID : ENSAPOG00000005277
Gene Symbol: CCKAR
4 Cross references
201 Possible Orthologues:

Cholecystokinin Receptor-Like

Ensembl ID : ENSAPOG00000006355
Gene Symbol: LOC110952247
3 Cross references
198 Possible Orthologues:

Cholesterol 24-Hydroxylase

Ensembl ID : ENSAPOG00000023330
Gene Symbol: LOC110951891
3 Cross references
259 Possible Orthologues:

Cholesteryl Ester Transfer Protein

Ensembl ID : ENSAPOG00000019644
Gene Symbol: CETP
3 Cross references
151 Possible Orthologues:


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).