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Query: NDUFAF2

RNAi screen result RNAPII IP (PI) CSB IP CSB IP (PI) Chrom. Chrom. (PI) Phosphorylation Ubiquitylation
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[Click on the plots to view the data selection in the respective scatterplot]

Protein Results:

 Results for post-translational modifications: see below | Red/green: hit at lower/upper end of the respective screen
Gene name Point score Z-score sums RNAi high RNAi low RNAPII-IP (PI) CSB-IP CSB-IP (PI) Chrom. Chrom. (PI)
NDUFAF2 0 -1.969 -0.810 0.580 -0.263 -0.281
NDUFAF2 0 -1.969 0.000 -0.110 -0.263 -0.281

PTM Sites:

 Back to Protein Results | Red/green: hit at lower/upper end of the respective screen
Gene name PTM type PTM site UV UV (PI) Sequence
NDUFAF2 Ubiquitylation K39 -2.005 _YYYIPQYK(gl)NWR_

Background Information for NDUFAF2:


Pubmed-NDUFAF2 »
Uniprot-NDUFAF2 »
Biogrid-NDUFAF2 »
ProteomicsDB-NDUFAF2 »

Tumorportal-NDUFAF2 »
COSMIC-NDUFAF2 »
GenomeRNAi-NDUFAF2 »
Genecards-NDUFAF2


Protein-protein Interactions for NDUFAF2
Show screen data for Category Name and Description Link to cat description Data Source
Category members IP bait ATXN3 Cat. description Hein, Mann, Cell 2015
Category members IP bait CHST15 Cat. description Hein, Mann, Cell 2015
Category members IP bait CBLN4 Cat. description BioPlex, Huttlin, Gygi, Cell 2015


Protein Domains in NDUFAF2
Domain name Domain Description TC-NER relevance -log10(p-value)


Protein complexes (CORUM database) featuring NDUFAF2
Category Type Category ID Category Name Data Source TC-NER relevance -log10(p-value)


Categories featuring NDUFAF2
Category Type Category ID Category Name Data Source TC-NER relevance -log10(p-value)
Category members GO Category GO:0005739 mitochondrion Database 1.67
Category members Pathway Pathway_65 PID_MYC_ACTIV_PATHWAY 0 1.08
Category members Disease phenotype MITOCHONDRIAL_COMPLEX_I_DEFICIENCY MITOCHONDRIAL COMPLEX I DEFICIENCY Database 0.35
Category members Disease phenotype Isolated_NADH-CoQ_reductase_deficiency Isolated NADH-CoQ reductase deficiency Database 0.17
Category members Disease phenotype Leigh_Syndrome_(nuclear_DNA_mutation) Leigh Syndrome (nuclear DNA mutation) Database 0.04
Category members GO Category GO:0061179 negative regulation of insulin secretion involved in cellular response to glucose stimulus Database 0


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