EcoDrugPlus

Tek Receptor Tyrosine Kinase

Ensembl ID : ENSPTIG00000010193
Gene Symbol: TEK
2 Cross references
164 Possible Orthologues:

Ttk Protein Kinase

Ensembl ID : ENSPTIG00000022073
Gene Symbol: TTK
2 Cross references
203 Possible Orthologues:

Udp-Glucose Ceramide Glucosyltransferase

Ensembl ID : ENSPTIG00000011415
Gene Symbol: UGCG
2 Cross references
211 Possible Orthologues:

Wee1 G2 Checkpoint Kinase

Ensembl ID : ENSPTIG00000014337
Gene Symbol: WEE1
2 Cross references
226 Possible Orthologues:

Yes Proto-Oncogene 1, Src Family Tyrosine Kinase

Ensembl ID : ENSPTIG00000014342
Gene Symbol: YES1
2 Cross references
268 Possible Orthologues:

Acetylcholinesterase (Cartwright Blood Group)

Ensembl ID : ENSPTIG00000013081
Gene Symbol: ACHE
2 Cross references
233 Possible Orthologues:

Activin A Receptor Like Type 1

Ensembl ID : ENSPTIG00000021376
Gene Symbol: ACVRL1
2 Cross references
353 Possible Orthologues:

Activin A Receptor Type 2b

Ensembl ID : ENSPTIG00000021345
Gene Symbol: ACVR2B
1 Cross references
257 Possible Orthologues:

Adenosine A1 Receptor

Ensembl ID : ENSPTIG00000021912
Gene Symbol: ADORA1
2 Cross references
269 Possible Orthologues:

Adenosine A2a Receptor

Ensembl ID : ENSPTIG00000013218
Gene Symbol: ADORA2A
2 Cross references
260 Possible Orthologues:

Adenosine A2b Receptor

Ensembl ID : ENSPTIG00000018799
Gene Symbol: ADORA2B
1 Cross references
200 Possible Orthologues:

Adenosine A3 Receptor

Ensembl ID : ENSPTIG00000022080
Gene Symbol: ADORA3
2 Cross references
89 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 from 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 from 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).