FAM133A and PRR13

Number of citations of the paper that reports this interaction (PMID 25416956)
0

Data Source:
BioGRID (two hybrid)

		FAM133A	PRR13
Gene Name		family with sequence similarity 133, member A	proline rich 13
Image		No pdb structure	No pdb structure
Gene Ontology Annotations	Cellular Component		Nucleus
	Molecular Function
	Biological Process		Transcription, DNA-templated Regulation Of Transcription, DNA-templated
Pathways
Drugs
Diseases
GWAS
Protein-Protein Interactions		8 interactors: BEND7 CEP70 NOS1AP PRR13 SDCBP2 STAC3 THAP1 TRIM23	24 interactors: BAIAP2 EWSR1 FAM133A GPAA1 KLHL12 KRTAP10-5 KRTAP10-7 KRTAP10-8 KRTAP4-12 LGALS3 LNX1 PEX5 PLSCR1 PPIA PSMA3 PSME3 RP9P RTN4 SDCBP SDCBP2 SRI TNFAIP8 VAC14 ZCCHC10
Entrez ID		286499	54458
HPRD ID		06562	13211
Ensembl ID		ENSG00000179083	ENSG00000205352
Uniprot IDs		Q8N9E0	F8VRX0 Q9NZ81
PDB IDs
Enriched GO Terms of Interacting Partners?		Positive Regulation Of Nitric Oxide Mediated Signal Transduction Positive Regulation Of Peptidyl-cysteine S-nitrosylation Regulation Of Generation Of L-type Calcium Current Positive Regulation Of Delayed Rectifier Potassium Channel Activity Regulation Of High Voltage-gated Calcium Channel Activity Regulation Of Cardiac Muscle Cell Action Potential Regulation Of Delayed Rectifier Potassium Channel Activity Regulation Of Heart Rate By Chemical Signal Positive Regulation Of Potassium Ion Transmembrane Transporter Activity Regulation Of Ventricular Cardiac Muscle Cell Membrane Repolarization	Negative Regulation Of Canonical Wnt Signaling Pathway Endomembrane System Organization Cell Migration Membrane Organization Cell Motility Negative Regulation Of Wnt Signaling Pathway Glycerophospholipid Biosynthetic Process Endoplasmic Reticulum Organization Apoptotic Process Response To Stimulus Viral Process Regulation Of Canonical Wnt Signaling Pathway Programmed Cell Death Phospholipid Biosynthetic Process Regulation Of Signaling Protein Ubiquitination Cell Death Death Negative Regulation Of Ubiquitin-protein Ligase Activity Involved In Mitotic Cell Cycle DNA Damage Response, Signal Transduction By P53 Class Mediator Resulting In Cell Cycle Arrest Protein Modification By Small Protein Conjugation Negative Regulation Of Immunological Synapse Formation Uncoating Of Virus Signal Transduction Involved In Mitotic G1 DNA Damage Checkpoint Cellular Localization Positive Regulation Of Ubiquitin-protein Ligase Activity Involved In Regulation Of Mitotic Cell Cycle Transition Signal Transduction Involved In DNA Damage Checkpoint Signal Transduction Involved In Cell Cycle Checkpoint Regulation Of Ubiquitin-protein Ligase Activity Involved In Mitotic Cell Cycle Negative Regulation Of Ubiquitin-protein Transferase Activity Regulation Of Cellular Process Regulation Of Viral Genome Replication Anaphase-promoting Complex-dependent Proteasomal Ubiquitin-dependent Protein Catabolic Process Glycerophospholipid Metabolic Process Regulation Of Wnt Signaling Pathway Mitotic G1 DNA Damage Checkpoint Positive Regulation Of Ubiquitin-protein Transferase Activity Mitotic G1/S Transition Checkpoint G1 DNA Damage Checkpoint Positive Regulation Of Cell Cycle Arrest Positive Regulation Of Ligase Activity Cellular Component Assembly Locomotion Positive Regulation Of Secretion Negative Regulation Of Protein Homotetramerization Intracellular Sequestering Of Iron Ion Negative Regulation Of T Cell Activation Via T Cell Receptor Contact With Antigen Bound To MHC Molecule On Antigen Presenting Cell DNA Damage Response, Signal Transduction By P53 Class Mediator Positive Regulation Of Transport Positive Regulation Of Protein Ubiquitination Involved In Ubiquitin-dependent Protein Catabolic Process
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