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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:SRGAP2-KCNJ10

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: SRGAP2-KCNJ10
FusionPDB ID: 86368
FusionGDB2.0 ID: 86368
HgeneTgene
Gene symbol

SRGAP2

KCNJ10

Gene ID

23380

3766

Gene nameSLIT-ROBO Rho GTPase activating protein 2potassium inwardly rectifying channel subfamily J member 10
SynonymsARHGAP34|FNBP2|SRGAP2A|SRGAP3BIRK-10|KCNJ13-PEN|KIR1.2|KIR4.1|SESAME
Cytomap

1q32.1

1q23.2

Type of geneprotein-codingprotein-coding
DescriptionSLIT-ROBO Rho GTPase-activating protein 2SLIT-ROBO GAP2formin-binding protein 2rho GTPase-activating protein 34ATP-sensitive inward rectifier potassium channel 10ATP-dependent inwardly rectifying potassium channel Kir4.1glial ATP-dependent inwardly rectifying potassium channel KIR4.1inward rectifier K(+) channel Kir1.2inward rectifier K+ channel KIR1.2potassi
Modification date2020031320200322
UniProtAcc.

P78508

Ensembl transtripts involved in fusion geneENST idsENST00000414007, ENST00000419187, 
ENST00000471256, 
ENST00000509700, 
ENST00000368089, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score11 X 7 X 7=5393 X 3 X 2=18
# samples 113
** MAII scorelog2(11/539*10)=-2.29278174922785
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context (manual curation of fusion genes in FusionPDB)

PubMed: SRGAP2 [Title/Abstract] AND KCNJ10 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)SRGAP2(206610392)-KCNJ10(160012322), # samples:2
Anticipated loss of major functional domain due to fusion event.SRGAP2-KCNJ10 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
SRGAP2-KCNJ10 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
* 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
HgeneSRGAP2

GO:0043547

positive regulation of GTPase activity

21148482

HgeneSRGAP2

GO:0046847

filopodium assembly

22559944

HgeneSRGAP2

GO:0051014

actin filament severing

21148482

HgeneSRGAP2

GO:0060996

dendritic spine development

22559944

HgeneSRGAP2

GO:2001223

negative regulation of neuron migration

22559944


check buttonFusion gene breakpoints across SRGAP2 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across KCNJ10 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4CESCTCGA-VS-A957-01ASRGAP2chr1

206610392

-KCNJ10chr1

160012322

-
ChimerDB4CESCTCGA-VS-A957-01ASRGAP2chr1

206610392

+KCNJ10chr1

160012322

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000414007SRGAP2chr1206610392+ENST00000368089KCNJ10chr1160012322-62791213361394452

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score
ENST00000414007ENST00000368089SRGAP2chr1206610392+KCNJ10chr1160012322-0.000529360.99947065

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>86368_86368_1_SRGAP2-KCNJ10_SRGAP2_chr1_206610392_ENST00000414007_KCNJ10_chr1_160012322_ENST00000368089_length(amino acids)=452AA_BP=392
MMKVLNELYSVMKTYHMYNADSISAQSKLKEAEKQEEKQIGKSVKQEDRQTPRSPDSTANVRIEEKHVRRSSVKKIEKMKEKRQAKYTEN
KLKAIKARNEYLLALEATNASVFKYYIHDLSDLIDQCCDLGYHASLNRALRTFLSAELNLEQSKHEGLDAIENAVENLDATSDKQRLMEM
YNNVFCPPMKFEFQPHMGDMASQLCAQQPVQSELVQRCQQLQSRLSTLKIENEEVKKTMEATLQTIQDIVTVEDFDVSDCFQYSNSMESV
KSTVSETFMSKPSIAKRRANQQETEQFYFTKMKEYLEGRNLITKLQAKHDLLQKTLGESQRTDCSLARRSSTVRKQDSSQAIPLVVESCI
RFISRHGLQHEGIFRVSGSQVEVNDIKNAFERDDVSCQGVLQSDHSDRKPAPNGPRDTTAESPDKRWSQQRENGAHCRQALPLPQGPVDN

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr1:206610392/chr1:160012322)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.KCNJ10

P78508

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: May be responsible for potassium buffering action of glial cells in the brain. Inward rectifier potassium channels are characterized by a greater tendency to allow potassium to flow into the cell rather than out of it. Their voltage dependence is regulated by the concentration of extracellular potassium; as external potassium is raised, the voltage range of the channel opening shifts to more positive voltages. The inward rectification is mainly due to the blockage of outward current by internal magnesium. Can be blocked by extracellular barium and cesium (By similarity). In the kidney, together with KCNJ16, mediates basolateral K(+) recycling in distal tubules; this process is critical for Na(+) reabsorption at the tubules. {ECO:0000250, ECO:0000305|PubMed:24561201}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneKCNJ10chr1:206610392chr1:160012322ENST0000036808902115_1260.0380.0IntramembraneHelical%3B Pore-forming%3B Name%3DH5
TgeneKCNJ10chr1:206610392chr1:160012322ENST0000036808902127_1330.0380.0IntramembranePore-forming
TgeneKCNJ10chr1:206610392chr1:160012322ENST0000036808902128_1330.0380.0MotifSelectivity filter
TgeneKCNJ10chr1:206610392chr1:160012322ENST0000036808902210_2170.0380.0Nucleotide bindingATP
TgeneKCNJ10chr1:206610392chr1:160012322ENST0000036808902134_1420.0380.0Topological domainExtracellular
TgeneKCNJ10chr1:206610392chr1:160012322ENST0000036808902165_3790.0380.0Topological domainCytoplasmic
TgeneKCNJ10chr1:206610392chr1:160012322ENST00000368089021_640.0380.0Topological domainCytoplasmic
TgeneKCNJ10chr1:206610392chr1:160012322ENST000003680890290_1140.0380.0Topological domainExtracellular
TgeneKCNJ10chr1:206610392chr1:160012322ENST0000036808902143_1640.0380.0TransmembraneHelical%3B Name%3DM2
TgeneKCNJ10chr1:206610392chr1:160012322ENST000003680890265_890.0380.0TransmembraneHelical%3B Name%3DM1

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
SRGAP2
KCNJ10


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to SRGAP2-KCNJ10


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to SRGAP2-KCNJ10


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource