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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 23842

FusionGeneSummary for NDUFA7_PRKCG

check button Fusion gene summary
Fusion gene informationFusion gene name: NDUFA7_PRKCG
Fusion gene ID: 23842
HgeneTgene
Gene symbol

NDUFA7

PRKCG

Gene ID

4701

5582

Gene nameNADH:ubiquinone oxidoreductase subunit A7protein kinase C gamma
SynonymsB14.5a|CI-B14.5aPKC-gamma|PKCC|PKCG|SCA14
Cytomap

19p13.2

19q13.42

Type of geneprotein-codingprotein-coding
DescriptionNADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 7NADH dehydrogenase (ubiquinone) 1 alpha subcomplex, 7, 14.5kDaNADH-ubiquinone oxidoreductase subunit B14.5acomplex I B14.5a subunitprotein kinase C gamma type
Modification date2018052320180523
UniProtAcc

O95182

P05129

Ensembl transtripts involved in fusion geneENST00000598884, ENST00000301457, 
ENST00000536044, ENST00000540413, 
ENST00000263431, ENST00000542049, 
Fusion gene scores* DoF score3 X 2 X 3=181 X 1 X 1=1
# samples 31
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: NDUFA7 [Title/Abstract] AND PRKCG [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
TgenePRKCG

GO:0016310

phosphorylation

15808853

TgenePRKCG

GO:0031397

negative regulation of protein ubiquitination

15808853

TgenePRKCG

GO:0032425

positive regulation of mismatch repair

15808853

TgenePRKCG

GO:0042177

negative regulation of protein catabolic process

15808853


check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* All genome coordinats were lifted-over on hg19.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGARVHNSCTCGA-D6-6515-01ANDUFA7chr19

8381380

-PRKCGchr19

54406327

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
5CDS-intronENST00000598884ENST00000536044NDUFA7chr19

8381380

-PRKCGchr19

54406327

+
5CDS-intronENST00000598884ENST00000540413NDUFA7chr19

8381380

-PRKCGchr19

54406327

+
5CDS-intronENST00000598884ENST00000263431NDUFA7chr19

8381380

-PRKCGchr19

54406327

+
5CDS-intronENST00000598884ENST00000542049NDUFA7chr19

8381380

-PRKCGchr19

54406327

+
5CDS-intronENST00000301457ENST00000536044NDUFA7chr19

8381380

-PRKCGchr19

54406327

+
5CDS-intronENST00000301457ENST00000540413NDUFA7chr19

8381380

-PRKCGchr19

54406327

+
5CDS-intronENST00000301457ENST00000263431NDUFA7chr19

8381380

-PRKCGchr19

54406327

+
5CDS-intronENST00000301457ENST00000542049NDUFA7chr19

8381380

-PRKCGchr19

54406327

+

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FusionProtFeatures for NDUFA7_PRKCG


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NDUFA7

O95182

PRKCG

P05129

Accessory subunit of the mitochondrial membranerespiratory chain NADH dehydrogenase (Complex I), that is believednot to be involved in catalysis. Complex I functions in thetransfer of electrons from NADH to the respiratory chain. Theimmediate electron acceptor for the enzyme is believed to beubiquinone. {ECO:0000269|PubMed:27626371}. Calcium-activated, phospholipid- and diacylglycerol(DAG)-dependent serine/threonine-protein kinase that plays diverseroles in neuronal cells and eye tissues, such as regulation of theneuronal receptors GRIA4/GLUR4 and GRIN1/NMDAR1, modulation ofreceptors and neuronal functions related to sensitivity toopiates, pain and alcohol, mediation of synaptic function and cellsurvival after ischemia, and inhibition of gap junction activityafter oxidative stress. Binds and phosphorylates GRIA4/GLUR4glutamate receptor and regulates its function by increasing plasmamembrane-associated GRIA4 expression. In primary cerebellarneurons treated with the agonist 3,5-dihyidroxyphenylglycine,functions downstream of the metabotropic glutamate receptorGRM5/MGLUR5 and phosphorylates GRIN1/NMDAR1 receptor which plays akey role in synaptic plasticity, synaptogenesis, excitotoxicity,memory acquisition and learning. May be involved in the regulationof hippocampal long-term potentiation (LTP), but may be notnecessary for the process of synaptic plasticity. May be involvedin desensitization of mu-type opioid receptor-mediated G-proteinactivation in the spinal cord, and may be critical for thedevelopment and/or maintenance of morphine-induced reinforcingeffects in the limbic forebrain. May modulate the functionality ofmu-type-opioid receptors by participating in a signaling pathwaywhich leads to the phosphorylation and degradation of opioidreceptors. May also contributes to chronic morphine-inducedchanges in nociceptive processing. Plays a role in neuropathicpain mechanisms and contributes to the maintenance of theallodynia pain produced by peripheral inflammation. Plays animportant role in initial sensitivity and tolerance to ethanol, bymediating the behavioral effects of ethanol as well as the effectsof this drug on the GABA(A) receptors. During and after cerebralischemia modulate neurotransmission and cell survival in synapticmembranes, and is involved in insulin-induced inhibition ofnecrosis, an important mechanism for minimizing ischemic injury.Required for the elimination of multiple climbing fibers duringinnervation of Purkinje cells in developing cerebellum. Isactivated in lens epithelial cells upon hydrogen peroxidetreatment, and phosphorylates connexin-43 (GJA1/CX43), resultingin disassembly of GJA1 gap junction plaques and inhibition of gapjunction activity which could provide a protective effect againstoxidative stress (By similarity). Phosphorylates p53/TP53 andpromotes p53/TP53-dependent apoptosis in response to DNA damage.Involved in the phase resetting of the cerebral cortex circadianclock during temporally restricted feeding. Stabilizes the coreclock component ARNTL/BMAL1 by interfering with itsubiquitination, thus suppressing its degradation, resulting inphase resetting of the cerebral cortex clock (By similarity).{ECO:0000250|UniProtKB:P63318, ECO:0000250|UniProtKB:P63319,ECO:0000269|PubMed:16377624}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page

.

* Minus value of BPloci means that the break pointn is located before the CDS.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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FusionGeneSequence for NDUFA7_PRKCG


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

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FusionGenePPI for NDUFA7_PRKCG


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page

.

check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors
NDUFA7PRKAB1, RPL38, TIMM44, RRBP1, PIN1, SBDS, RAB8A, PDLIM5, RBM27, MRRF, TAGLN, PIN4, RANGAP1, UBL4A, PDLIM7, TPX2, UBE2L3, SNX3, ECI2, HRSP12, RBMS1, SUGP1, QKI, PQBP1, KIAA0101, RPS10P5, TBL2, RFX5, STX7, MPLKIP, SNRPC, SCO2, NABP2, MRPS28, ZC3H11A, CDV3, MRPL14, OLA1, SRRM2, TOMM40, RPS28, UBE2I, GATAD2B, UBE4B, VDAC3, SCP2, ACAA1, NUP214, MDFI, UPF2, NDUFS3, TMX2, DNAJC30, GJA1, ENPP6, NDUFA8, VAPB, NDUFA12, NDUFS4, NDUFS5, NDUFA9, NDUFS6, RAB5C, RAB7A, VAPA, GOLT1B, MMGT1, NDUFA4, C15orf48, COX6B1, NDUFB11, NDUFS7, NDUFA13, SSMEM1, FUT1PRKCGYWHAG, GRIA4, RGS2, TIAM1, AFAP1, GABRA1, GABRA4, NFE2L2, PRKCG, DDX58, IBTK, PICK1, NOXA1, EXOC5, CCHCR1, TOP2A, APP, SDC2, ITGB2, HSP90AA1, GSK3A, CASR, ARHGEF25, RANBP10, GFAP, HSPA4, EPHB1, SCN3A, TRIM5, RANBP9, DAB2, CTNNB1, SMURF1, UBE2T, PRKCA


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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RelatedDrugs for NDUFA7_PRKCG


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for NDUFA7_PRKCG


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePRKCGC0020429Hyperalgesia2CTD_human
TgenePRKCGC0040997Trigeminal Neuralgia1CTD_human
TgenePRKCGC0087012Ataxia, Spinocerebellar1CTD_human
TgenePRKCGC1854369Spinocerebellar ataxia 141CTD_human;ORPHANET;UNIPROT
TgenePRKCGC3714756Intellectual Disability1CTD_human