EcoDrugPlus

Mapk Interacting Serine/threonine Kinase 2

Ensembl ID : ENSMOCG00000012080
Gene Symbol: MKNK2
3 Cross references
220 Possible Orthologues:

Mcl1 Apoptosis Regulator, Bcl2 Family Member

Ensembl ID : ENSMOCG00000000395
Gene Symbol: MCL1
3 Cross references
237 Possible Orthologues:

Mdm2 Proto-Oncogene

Ensembl ID : ENSMOCG00000008043
Gene Symbol: MDM2
3 Cross references
254 Possible Orthologues:

Met Proto-Oncogene, Receptor Tyrosine Kinase

Ensembl ID : ENSMOCG00000006344
Gene Symbol: MET
3 Cross references
211 Possible Orthologues:

Mpl Proto-Oncogene, Thrombopoietin Receptor

Ensembl ID : ENSMOCG00000015836
Gene Symbol: MPL
3 Cross references
186 Possible Orthologues:

Mtor Associated Protein, Lst8 Homolog

Ensembl ID : ENSMOCG00000022227
Gene Symbol: MLST8
3 Cross references
201 Possible Orthologues:

Nad(P)h Dehydrogenase [Quinone] 1

Ensembl ID : ENSMOCG00000019596
Gene Symbol: LOC101996668
2 Cross references
194 Possible Orthologues:

Nad(P)h Dehydrogenase [Quinone] 1

Ensembl ID : ENSMOCG00000009352
Gene Symbol: LOC102002710
2 Cross references
194 Possible Orthologues:

Nadph Oxidase 4

Ensembl ID : ENSMOCG00000003268
Gene Symbol: NOX4
3 Cross references
151 Possible Orthologues:

Npc1 Like Intracellular Cholesterol Transporter 1

Ensembl ID : ENSMOCG00000022891
Gene Symbol: NPC1L1
3 Cross references
189 Possible Orthologues:

Pim-1 Proto-Oncogene, Serine/threonine Kinase

Ensembl ID : ENSMOCG00000019644
Gene Symbol: PIM1
3 Cross references
244 Possible Orthologues:

Pim-2 Proto-Oncogene, Serine/threonine Kinase

Ensembl ID : ENSMOCG00000005351
Gene Symbol: PIM2
3 Cross references
115 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).