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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:SRCIN1-KRT39 (FusionGDB2 ID:85668)

Fusion Gene Summary for SRCIN1-KRT39

check button Fusion gene summary
Fusion gene informationFusion gene name: SRCIN1-KRT39
Fusion gene ID: 85668
HgeneTgene
Gene symbol

SRCIN1

KRT39

Gene ID

80725

390792

Gene nameSRC kinase signaling inhibitor 1keratin 39
SynonymsP140|SNIPCK-39|K39|KA35
Cytomap

17q12

17q21.2

Type of geneprotein-codingprotein-coding
DescriptionSRC kinase signaling inhibitor 1P130Cas-associated proteinSNAP-25-interacting proteinSNAP25-interacting proteinp140Capkeratin, type I cytoskeletal 39cytokeratin-39keratin 39, type Itype I hair keratin KA35
Modification date2020032020200313
UniProtAcc..
Ensembl transtripts involved in fusion geneENST00000264659, ENST00000578925, 
ENST00000398579, 
ENST00000355612, 
Fusion gene scores* DoF score10 X 14 X 6=8402 X 2 X 2=8
# samples 112
** MAII scorelog2(11/840*10)=-2.93288580414146
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: SRCIN1 [Title/Abstract] AND KRT39 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointSRCIN1(36728915)-KRT39(39115111), # samples:2
Anticipated loss of major functional domain due to fusion event.
* 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
HgeneSRCIN1

GO:0061098

positive regulation of protein tyrosine kinase activity

17525734

HgeneSRCIN1

GO:0061099

negative regulation of protein tyrosine kinase activity

17525734


check buttonFusion gene breakpoints across SRCIN1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across KRT39 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4READTCGA-EI-6509SRCIN1chr17

36728915

-KRT39chr17

39115111

-
ChimerDB4READTCGA-EI-6509SRCIN1chr17

36731123

-KRT39chr17

39115111

-
ChimerDB4READTCGA-EI-6509-01ASRCIN1chr17

36728915

-KRT39chr17

39115111

-


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Fusion Gene ORF analysis for SRCIN1-KRT39

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
intron-3CDSENST00000264659ENST00000355612SRCIN1chr17

36728915

-KRT39chr17

39115111

-
intron-3CDSENST00000578925ENST00000355612SRCIN1chr17

36728915

-KRT39chr17

39115111

-
5UTR-3CDSENST00000398579ENST00000355612SRCIN1chr17

36728915

-KRT39chr17

39115111

-
intron-3CDSENST00000264659ENST00000355612SRCIN1chr17

36731123

-KRT39chr17

39115111

-
In-frameENST00000578925ENST00000355612SRCIN1chr17

36731123

-KRT39chr17

39115111

-
intron-3CDSENST00000398579ENST00000355612SRCIN1chr17

36731123

-KRT39chr17

39115111

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000578925SRCIN1chr1736731123-ENST00000355612KRT39chr1739115111-10035606601220

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
ENST00000578925ENST00000355612SRCIN1chr1736731123-KRT39chr1739115111-0.3973460.602654

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Fusion Genomic Features for SRCIN1-KRT39


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for SRCIN1-KRT39


check button Go to

FGviewer for the breakpoints of chr17:36731123-chr17:39115111

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

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

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
TgeneKRT39chr17:36731123chr17:39115111ENST0000035561257404_491405.6666666666667492.0RegionNote=Tail

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneSRCIN1chr17:36731123chr17:39115111ENST00000264659-119654_67401184.0Coiled coilOntology_term=ECO:0000255
HgeneSRCIN1chr17:36731123chr17:39115111ENST00000264659-119726_74601184.0Coiled coilOntology_term=ECO:0000255
HgeneSRCIN1chr17:36731123chr17:39115111ENST00000264659-119471_50401184.0Compositional biasNote=Pro-rich
HgeneSRCIN1chr17:36731123chr17:39115111ENST00000264659-119956_101401184.0Compositional biasNote=Pro-rich
TgeneKRT39chr17:36731123chr17:39115111ENST000003556125796_407405.6666666666667492.0DomainIF rod
TgeneKRT39chr17:36731123chr17:39115111ENST0000035561257132_142405.6666666666667492.0RegionNote=Linker 1
TgeneKRT39chr17:36731123chr17:39115111ENST0000035561257143_243405.6666666666667492.0RegionNote=Coil 1B
TgeneKRT39chr17:36731123chr17:39115111ENST00000355612571_96405.6666666666667492.0RegionNote=Head
TgeneKRT39chr17:36731123chr17:39115111ENST0000035561257244_259405.6666666666667492.0RegionNote=Linker 12
TgeneKRT39chr17:36731123chr17:39115111ENST0000035561257260_403405.6666666666667492.0RegionNote=Coil 2
TgeneKRT39chr17:36731123chr17:39115111ENST000003556125797_131405.6666666666667492.0RegionNote=Coil 1A


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Fusion Gene Sequence for SRCIN1-KRT39


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>In-frame_ENST00000578925_ENST00000355612_TCGA-EI-6509_SRCIN1_chr17_36731123_-_KRT39_chr17_39115111_length(transcript)=1003nt_BP=560nt
GGCGGGGCCCGCGCCCCCGGCCCGCCCGCCTGGCACCGCGCCCCGGGGCTGGGGCCGAGCGAGGAGCCCGCGAGGCGGCGAGAGGGCGAG
CGCCAGGCAGGCCGGCCCGGGGCCCCCGCCCCCCGCGCCCCCGCCCGATGGGGAACGCTCCGTCCCAAGATCCGGAGCGGAGCAGCCCCC
CCATGCTGTCTGCGGACGATGCGGAGTACCCGCGGGAGTACCGGACCCTGGGGGGCGGGGGCGGCGGGGGCAGCGGGGGCCGGCGCTTCT
CCAACGTGGGGCTGGTGCACACGTCCGAGCGGCGGCACACGGTGATCGCGGCCCAGAGTCTGGAGGCGCTCAGCGGGCTCCAGAAGGCGG
ACGCCGACCGCAAGCGTGATGCCTTCATGGACCACCTGAAGAGCAAGTACCCACAGCACGCCCTGGCCCTGCGAGGCCAGCAGGACAGGA
TGCGAGAGCAGGTTGGCGGCTGGACCGTGGACCCCGTATGCCTCCTCAGCTCCCTCTGCTCCCACCTCCATGGCGACTCCGCCCCCTCCG
GGGCTGGCCAGCCGGCCCAGGCGTCCCTGTTACCCACGTGCCACCAAATGTGAGCCTTCCCCTTGGACATCTTGTAAGTCCGGAGCCATA
GAAAGCACGGCCCCAGCTTGCACATCCTCATCCCCCTGCAGCTTAAAGGAGCACTGCAGTGCCTGCGGACCCCTGTCCCGGATACTGGTT
AAAATTTGCACCATCACCAAGGAGATTAAGGATGGGAAGGTCATTTCTTCTTACGAGCATGTGCAGCCTTGTTTCATCATCAGACCTGCC
AAAGTCTAACATCCCAAGGTGATGAAAATGACCCACATTTATGAAACAGAGGCCAATACATGCTCCTGCCAGAGAGGTTTAAGAAAACTC
CCCAGTCCCTTAAGGTACTTAGTTTCTTACTACTACAGCGGGTCCCCATTGCTAGGTAGAATATCTTTTATTCTGCTCCTTCCCTAACTC

>In-frame_ENST00000578925_ENST00000355612_TCGA-EI-6509_SRCIN1_chr17_36731123_-_KRT39_chr17_39115111_length(amino acids)=220AA_start in transcript=660_stop in transcript=1
MRMCKLGPCFLWLRTYKMSKGKAHIWWHVGNRDAWAGWPAPEGAESPWRWEQRELRRHTGSTVQPPTCSRILSCWPRRARACCGYLLFRW
SMKASRLRSASAFWSPLSASRLWAAITVCRRSDVCTSPTLEKRRPPLPPPPPPPRVRYSRGYSASSADSMGGLLRSGSWDGAFPIGRGRG

--------------------------------------------------------------

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Fusion Gene PPI Analysis for SRCIN1-KRT39


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


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
HgeneSRCIN1chr17:36731123chr17:39115111ENST00000264659-119647_69701184.0SNAP25


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


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Related Drugs for SRCIN1-KRT39


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for SRCIN1-KRT39


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSRCIN1C0009171Cocaine Abuse1CTD_human
HgeneSRCIN1C0236736Cocaine-Related Disorders1CTD_human
HgeneSRCIN1C0600427Cocaine Dependence1CTD_human