PDE4DIP - New-wiki

Interactant Symbol	Name	Associated Pathways Hide	Binding Drugs Hide	Associated Diseases Hide
CDKN1A	cyclin dependent kinase inhibitor 1A	SCF(Skp2)-mediated degradation of p27/p21 AKT phosphorylates targets in the cytosol Senescence-Associated Secretory Phenotype (SASP) DNA Damage/Telomere Stress Induced Senescence Constitutive Signaling by AKT1 E17K in Cancer Interleukin-4 and Interleukin-13 signaling TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest Cyclin E associated events during G1/S transition Cyclin D associated events in G1 p53-Dependent G1 DNA Damage Response Cyclin A:Cdk2-associated events at S phase entry Transcriptional activation of cell cycle inhibitor p21 The role of GTSE1 in G2/M progression after G2 checkpoint TFAP2 (AP-2) family regulates transcription of cell cycle factors Transcriptional regulation by RUNX2 RUNX3 regulates CDKN1A transcription Neddylation Transcriptional regulation of granulopoiesis FOXO-mediated transcription of cell cycle genes Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) STAT5 activation downstream of FLT3 ITD mutants Signaling by FLT3 fusion proteins Signaling by ALK fusions and activated point mutants KEAP1-NFE2L2 pathway Regulation of MITF-M-dependent genes involved in cell cycle and proliferation	Valproic acid Arsenic trioxide	Cervical cancer
CHCHD3	coiled-coil-helix-coiled-coil-helix domain containing 3	Mitochondrial protein import Cristae formation
CLIP4	CAP-Gly domain containing linker protein family member 4
CWF19L2	CWF19 like cell cycle control factor 2	mRNA Splicing - Major Pathway
DSCAM	DS cell adhesion molecule	DSCAM interactions DSCAM interactions
DSCR9	Down syndrome critical region 9
EGR2	early growth response 2	Transcriptional regulation of white adipocyte differentiation Activation of anterior HOX genes in hindbrain development during early embryogenesis NGF-stimulated transcription NGF-stimulated transcription EGR2 and SOX10-mediated initiation of Schwann cell myelination EGR2 and SOX10-mediated initiation of Schwann cell myelination		Charcot-Marie-Tooth disease (CMT); Hereditary motor and sensory neuropathy; Peroneal muscular atrophy
FAM161A	FAM161 centrosomal protein A			Retinitis pigmentosa (RP)
FAM50B	family with sequence similarity 50 member B
FAM74A4	family with sequence similarity 74 member A4
FCHSD2	FCH and double SH3 domains 2
FES	FES proto-oncogene, tyrosine kinase	Signaling by SCF-KIT Sema3A PAK dependent Axon repulsion SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion CRMPs in Sema3A signaling	Fostamatinib
FHL1	four and a half LIM domains 1			X-linked myopathy with postural muscle atrophy (XMPMA) Scapuloperoneal myopathy (SPM) Reducing body myopathy (RBM) Emery-Dreifuss muscular dystrophy
GADD45G	growth arrest and DNA damage inducible gamma
GFI1B	growth factor independent 1B transcriptional repressor
GOLGA8EP	golgin A8 family member E, pseudogene
GOLGA8F	golgin A8 family member F
HAUS1	HAUS augmin like complex subunit 1	Regulation of PLK1 Activity at G2/M Transition Loss of Nlp from mitotic centrosomes Recruitment of mitotic centrosome proteins and complexes Loss of proteins required for interphase microtubule organization from the centrosome Recruitment of NuMA to mitotic centrosomes Anchoring of the basal body to the plasma membrane AURKA Activation by TPX2
HOXB5	homeobox B5
HOXC8	homeobox C8	Regulation of CDH11 gene transcription Regulation of CDH11 gene transcription

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