SRPK2 - Wiki-Pi

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421 interactions involving SRPK2 - SRSF protein kinase 2 found:

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Symbol	Description	Pathways Hide	Drugs Hide	Diseases Hide
DOCK3	dedicator of cytokinesis 3	RAC1 GTPase cycle RAC2 GTPase cycle RHOG GTPase cycle NTRK2 activates RAC1 NTRK2 activates RAC1 Factors involved in megakaryocyte development and platelet production
DRAP1	DR1 associated protein 1	Signaling by NODAL Signaling by Activin
DRG1	developmentally regulated GTP binding protein 1	Protein hydroxylation
DYRK1A	dual specificity tyrosine phosphorylation regulated kinase 1A	G0 and Early G1	N-(5-{[(2S)-4-amino-2-(3-chlorophenyl)butanoyl]amino}-1H-indazol-3-yl)benzamide Fostamatinib
ECT2	epithelial cell transforming 2	NRAGE signals death through JNK G alpha (12/13) signalling events RHOA GTPase cycle RHOB GTPase cycle CDC42 GTPase cycle RAC1 GTPase cycle
EED	embryonic ectoderm development	PRC2 methylates histones and DNA Oxidative Stress Induced Senescence PKMTs methylate histone lysines Activation of anterior HOX genes in hindbrain development during early embryogenesis Regulation of PTEN gene transcription Regulation of PTEN gene transcription Transcriptional Regulation by E2F6 HCMV Early Events Defective pyroptosis Negative Regulation of CDH1 Gene Transcription Regulation of PD-L1(CD274) transcription
EFCAB12	EF-hand calcium binding domain 12
EGLN2	egl-9 family hypoxia inducible factor 2	Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha	Ascorbic acid Roxadustat Daprodustat Vadadustat
EIF1AY	eukaryotic translation initiation factor 1A Y-linked
EIF3A	eukaryotic translation initiation factor 3 subunit A	L13a-mediated translational silencing of Ceruloplasmin expression Translation initiation complex formation Formation of a pool of free 40S subunits Formation of the ternary complex, and subsequently, the 43S complex Ribosomal scanning and start codon recognition GTP hydrolysis and joining of the 60S ribosomal subunit
EIF4B	eukaryotic translation initiation factor 4B	L13a-mediated translational silencing of Ceruloplasmin expression mTORC1-mediated signalling Deadenylation of mRNA Deadenylation of mRNA Translation initiation complex formation Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Ribosomal scanning and start codon recognition GTP hydrolysis and joining of the 60S ribosomal subunit M-decay: degradation of maternal mRNAs by maternally stored factors Z-decay: degradation of maternal mRNAs by zygotically expressed factors
EIF4G1	eukaryotic translation initiation factor 4 gamma 1	ISG15 antiviral mechanism L13a-mediated translational silencing of Ceruloplasmin expression mTORC1-mediated signalling Deadenylation of mRNA Deadenylation of mRNA AUF1 (hnRNP D0) binds and destabilizes mRNA Translation initiation complex formation Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S Ribosomal scanning and start codon recognition GTP hydrolysis and joining of the 60S ribosomal subunit Regulation of expression of SLITs and ROBOs Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) M-decay: degradation of maternal mRNAs by maternally stored factors Z-decay: degradation of maternal mRNAs by zygotically expressed factors
ELAVL3	ELAV like RNA binding protein 3
ELP6	elongator acetyltransferase complex subunit 6	HATs acetylate histones
ENOX2	ecto-NOX disulfide-thiol exchanger 2		Idronoxil
ENSA	endosulfine alpha	MASTL Facilitates Mitotic Progression MASTL Facilitates Mitotic Progression
EPB41L1	erythrocyte membrane protein band 4.1 like 1	Trafficking of AMPA receptors Neurexins and neuroligins Sensory processing of sound by inner hair cells of the cochlea Sensory processing of sound by outer hair cells of the cochlea
EPB41L4A	erythrocyte membrane protein band 4.1 like 4A
EPB41L4B	erythrocyte membrane protein band 4.1 like 4B
EPM2A	EPM2A glucan phosphatase, laforin	Glycogen synthesis Myoclonic epilepsy of Lafora		Progressive myoclonic epilepsy (PME), including: Lafora disease (LBD); Unverricht-Lundborg disease (ULD); Neuronal ceroid lipofuscinoses (NCL); Type I sialidosis; Action myoclonus-renal failure syndrome (AMRF); Type III Gaucher disease (GD)

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