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Query: MT-ND1

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)
MT-ND1 0 1.104 0.684 0.420

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

Background Information for MT-ND1:


Pubmed-MT-ND1 »
Uniprot-MT-ND1 »
Biogrid-MT-ND1 »
ProteomicsDB-MT-ND1 »

Tumorportal-MT-ND1 »
COSMIC-MT-ND1 »
GenomeRNAi-MT-ND1 »
Genecards-MT-ND1


Protein-protein Interactions for MT-ND1
Show screen data for Category Name and Description Link to cat description Data Source


Protein Domains in MT-ND1
Domain name Domain Description TC-NER relevance -log10(p-value)


Protein complexes (CORUM database) featuring MT-ND1
Category Type Category ID Category Name Data Source TC-NER relevance -log10(p-value)
Category members Corum 2939 Ecsit complex (ECSIT, MT-CO2, NDUFA1, MT-ND1, TRAF6, NDUFAF1) Database 0.09


Categories featuring MT-ND1
Category Type Category ID Category Name Data Source TC-NER relevance -log10(p-value)
Category members GO Category GO:0005515 protein binding Database INF
Category members GO Category GO:0016021 integral to membrane Database 7.67
Category members GO Category GO:0005739 mitochondrion Database 1.67
Category members GO Category GO:0016020 membrane Database 0.52
Category members GO Category GO:0044281 small molecule metabolic process Database 0.35
Category members GO Category GO:0022904 respiratory electron transport chain Database 0.15
Category members GO Category GO:0005743 mitochondrial inner membrane Database 0.15
Category members Disease phenotype Leber_hereditary_optic_neuropathy Leber hereditary optic neuropathy Database 0.13
Category members Disease phenotype LEBER_OPTIC_ATROPHY LEBER OPTIC ATROPHY Database 0.13
Category members GO Category GO:0008137 NADH dehydrogenase (ubiquinone) activity Database 0.11
Category members GO Category GO:0044237 cellular metabolic process Database 0.08
Category members GO Category GO:0005747 mitochondrial respiratory chain complex I Database 0.08
Category members Disease phenotype MITOCHONDRIAL_MYOPATHY_ENCEPHALOPATHY_LACTIC_ACIDOSIS_AND_STROKE-LIKE MITOCHONDRIAL MYOPATHY ENCEPHALOPATHY LACTIC ACIDOSIS AND STROKE-LIKE Database 0.08
Category members GO Category GO:0006120 mitochondrial electron transport, NADH to ubiquinone Database 0.07
Category members Disease phenotype ALZHEIMER_DISEASE_SUSCEPTIBILITY_TO_MITOCHONDRIAL ALZHEIMER DISEASE SUSCEPTIBILITY TO MITOCHONDRIAL Database 0.05
Category members Disease phenotype Maternally-inherited_Leigh_syndrome Maternally-inherited Leigh syndrome Database 0.01
Category members Disease phenotype MELAS_SYNDROME MELAS SYNDROME Database 0
Category members GO Category GO:0031966 mitochondrial membrane Database 0
Category members GO Category GO:0055114 oxidation-reduction process Database 0


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