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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:HNRNPL-ACTN4 (FusionGDB2 ID:37241)

Fusion Gene Summary for HNRNPL-ACTN4

check button Fusion gene summary
Fusion gene informationFusion gene name: HNRNPL-ACTN4
Fusion gene ID: 37241
HgeneTgene
Gene symbol

HNRNPL

ACTN4

Gene ID

3191

81

Gene nameheterogeneous nuclear ribonucleoprotein Lactinin alpha 4
SynonymsHNRPL|P/OKcl.14|hnRNP-LACTININ-4|FSGS|FSGS1
Cytomap

19q13.2

19q13.2

Type of geneprotein-codingprotein-coding
Descriptionheterogeneous nuclear ribonucleoprotein Lepididymis secretory sperm binding proteinhnRNP Lalpha-actinin-4focal segmental glomerulosclerosis 1non-muscle alpha-actinin 4
Modification date2020031320200327
UniProtAcc

P14866

O43707

Ensembl transtripts involved in fusion geneENST00000221419, ENST00000600873, 
ENST00000390009, ENST00000424234, 
ENST00000497637, ENST00000252699, 
Fusion gene scores* DoF score17 X 19 X 9=290727 X 38 X 12=12312
# samples 1948
** MAII scorelog2(19/2907*10)=-3.93545974780529
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(48/12312*10)=-4.68088692071969
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: HNRNPL [Title/Abstract] AND ACTN4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHNRNPL(39340340)-ACTN4(39205109), # 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
TgeneACTN4

GO:0033209

tumor necrosis factor-mediated signaling pathway

25411248

TgeneACTN4

GO:0035357

peroxisome proliferator activated receptor signaling pathway

22351778

TgeneACTN4

GO:0048384

retinoic acid receptor signaling pathway

22351778

TgeneACTN4

GO:0051272

positive regulation of cellular component movement

9508771


check buttonFusion gene breakpoints across HNRNPL (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 ACTN4 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

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
ChimerDB4OVTCGA-23-1107-01AHNRNPLchr19

39340340

-ACTN4chr19

39205109

+


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Fusion Gene ORF analysis for HNRNPL-ACTN4

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-intronENST00000221419ENST00000390009HNRNPLchr19

39340340

-ACTN4chr19

39205109

+
5CDS-intronENST00000221419ENST00000424234HNRNPLchr19

39340340

-ACTN4chr19

39205109

+
5CDS-intronENST00000221419ENST00000497637HNRNPLchr19

39340340

-ACTN4chr19

39205109

+
In-frameENST00000221419ENST00000252699HNRNPLchr19

39340340

-ACTN4chr19

39205109

+
intron-3CDSENST00000600873ENST00000252699HNRNPLchr19

39340340

-ACTN4chr19

39205109

+
intron-intronENST00000600873ENST00000390009HNRNPLchr19

39340340

-ACTN4chr19

39205109

+
intron-intronENST00000600873ENST00000424234HNRNPLchr19

39340340

-ACTN4chr19

39205109

+
intron-intronENST00000600873ENST00000497637HNRNPLchr19

39340340

-ACTN4chr19

39205109

+

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)
ENST00000221419HNRNPLchr1939340340-ENST00000252699ACTN4chr1939205109+47026343672550727

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
ENST00000221419ENST00000252699HNRNPLchr1939340340-ACTN4chr1939205109+0.0129197310.9870803

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Fusion Genomic Features for HNRNPL-ACTN4


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)
HNRNPLchr1939340339-ACTN4chr1939205108+5.15E-161
HNRNPLchr1939340339-ACTN4chr1939205108+5.15E-161

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.
genomic feature

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.
genomic feature of top 1%

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Fusion Protein Features for HNRNPL-ACTN4


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/chr19:39340340/chr19:39205109)
- 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
HNRNPL

P14866

ACTN4

O43707

FUNCTION: Splicing factor binding to exonic or intronic sites and acting as either an activator or repressor of exon inclusion. Exhibits a binding preference for CA-rich elements (PubMed:11809897, PubMed:22570490, PubMed:24164894, PubMed:25623890, PubMed:26051023). Component of the heterogeneous nuclear ribonucleoprotein (hnRNP) complexes and associated with most nascent transcripts (PubMed:2687284). Associates, together with APEX1, to the negative calcium responsive element (nCaRE) B2 of the APEX2 promoter (PubMed:11809897). {ECO:0000269|PubMed:11809897, ECO:0000269|PubMed:22570490, ECO:0000269|PubMed:25623890, ECO:0000269|PubMed:26051023, ECO:0000269|PubMed:2687284}.FUNCTION: F-actin cross-linking protein which is thought to anchor actin to a variety of intracellular structures. This is a bundling protein (Probable). Probably involved in vesicular trafficking via its association with the CART complex. The CART complex is necessary for efficient transferrin receptor recycling but not for EGFR degradation (PubMed:15772161). Involved in tight junction assembly in epithelial cells probably through interaction with MICALL2. Links MICALL2 to the actin cytoskeleton and recruits it to the tight junctions (By similarity). May also function as a transcriptional coactivator, stimulating transcription mediated by the nuclear hormone receptors PPARG and RARA (PubMed:22351778). {ECO:0000250|UniProtKB:P57780, ECO:0000269|PubMed:15772161, ECO:0000269|PubMed:22351778, ECO:0000305|PubMed:9508771}.

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
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000221419-11339_8989590.0Compositional biasNote=Gly-rich
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721778_789273912.0Calcium binding1
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721819_830273912.0Calcium binding2
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014778_78954693.0Calcium binding1
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014819_83054693.0Calcium binding2
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721765_800273912.0DomainEF-hand 1
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721806_841273912.0DomainEF-hand 2
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014163_26954693.0DomainCalponin-homology (CH) 2
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014765_80054693.0DomainEF-hand 1
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014806_84154693.0DomainEF-hand 2
TgeneACTN4chr19:39340340chr19:39205109ENST0000039000901484_8854693.0MotifLXXLL motif
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014177_19254693.0RegionPolyphosphoinositide (PIP2)-binding
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721293_403273912.0RepeatSpectrin 1
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721413_518273912.0RepeatSpectrin 2
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721528_639273912.0RepeatSpectrin 3
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721649_752273912.0RepeatSpectrin 4
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014293_40354693.0RepeatSpectrin 1
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014413_51854693.0RepeatSpectrin 2
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014528_63954693.0RepeatSpectrin 3
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014649_75254693.0RepeatSpectrin 4

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000221419-113335_38289590.0Compositional biasNote=Pro-rich
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000600873-113335_3820457.0Compositional biasNote=Pro-rich
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000600873-11339_890457.0Compositional biasNote=Gly-rich
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000221419-113102_17689590.0DomainRRM 1
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000221419-113193_27089590.0DomainRRM 2
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000221419-113382_47889590.0DomainRRM 3
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000221419-113495_58389590.0DomainRRM 4
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000600873-113102_1760457.0DomainRRM 1
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000600873-113193_2700457.0DomainRRM 2
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000600873-113382_4780457.0DomainRRM 3
HgeneHNRNPLchr19:39340340chr19:39205109ENST00000600873-113495_5830457.0DomainRRM 4
TgeneACTN4chr19:39340340chr19:39205109ENST0000025269972119_26273912.0Compositional biasPoly-Gly
TgeneACTN4chr19:39340340chr19:39205109ENST0000039000901419_2654693.0Compositional biasPoly-Gly
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721163_269273912.0DomainCalponin-homology (CH) 2
TgeneACTN4chr19:39340340chr19:39205109ENST0000025269972150_154273912.0DomainCalponin-homology (CH) 1
TgeneACTN4chr19:39340340chr19:39205109ENST0000039000901450_15454693.0DomainCalponin-homology (CH) 1
TgeneACTN4chr19:39340340chr19:39205109ENST0000025269972184_88273912.0MotifLXXLL motif
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721177_192273912.0RegionPolyphosphoinositide (PIP2)-binding
TgeneACTN4chr19:39340340chr19:39205109ENST000002526997211_269273912.0RegionNote=Actin-binding
TgeneACTN4chr19:39340340chr19:39205109ENST000003900090141_26954693.0RegionNote=Actin-binding


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Fusion Gene Sequence for HNRNPL-ACTN4


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.
>37241_37241_1_HNRNPL-ACTN4_HNRNPL_chr19_39340340_ENST00000221419_ACTN4_chr19_39205109_ENST00000252699_length(transcript)=4702nt_BP=634nt
GGAGACCAATGAAAGTGGGAGGGAGGCGGAGATTCTTGGGAGGTTTAGAGCGCCGTTCCTATCAGGTGCTTTTAGGGAGGCCAGCAGCGC
CAGAAATCCGACCTATCAAATTGGATTTTATTTTAAGGCGGCGGGGTCGACGGAAAGACTGGCAGAAAGCGACCACCTATAAGGAGTGTC
TCAGACAAACAAGGGCGGGCCCTCCTGCAGAACGGCGTGGGCAATGTCCAATAAGCGCGCAAGGCGTGTGGCGGCCTACCCTCCCCCCGC
GGCGGGACCAGTGGCTCCCCCTATCGGGTGGGGGCGGCGGGTGACGGGCGTGTCCCTCCCCCAATGAGAGGCGGGGGGAGGCGGGTTCTG
CGCCGCCATGTCGCGGAGGCTGCTGCCCCGGGCGGAGAAGCGGCGTCGGCGGCTGGAGCAGAGGCAGCAGCCGGACGAGCAGCGGAGGCG
GTCGGGAGCGATGGTGAAGATGGCGGCGGCGGGCGGCGGAGGCGGCGGTGGCCGCTACTACGGCGGCGGCAGTGAGGGCGGCCGGGCCCC
TAAGCGGCTCAAGACTGACAACGCCGGCGACCAGCACGGAGGCGGCGGCGGTGGCGGTGGAGGAGCCGGGGCGGCGGGCGGCGGCGGCGG
TGGGGCTGAAACTGCCGCCAACCGGATCTGTAAGGTGCTGGCTGTCAACCAAGAGAACGAGCACCTGATGGAGGACTACGAGAAGCTGGC
CAGCGACCTCCTGGAGTGGATCCGGCGCACCATCCCCTGGCTGGAGGACCGTGTGCCCCAAAAGACTATCCAGGAGATGCAGCAGAAGCT
GGAGGACTTCCGCGACTACCGGCGTGTGCACAAGCCGCCCAAGGTGCAGGAGAAGTGCCAGCTGGAGATCAACTTCAACACGCTGCAGAC
CAAGCTGCGCCTCAGCAACCGGCCCGCCTTCATGCCCTCCGAGGGCAAGATGGTCTCGGACATCAACAATGGCTGGCAGCACTTGGAGCA
GGCTGAGAAGGGCTACGAGGAGTGGCTGCTGAATGAGATCCGCAGGCTGGAGCGGCTCGACCACCTGGCAGAGAAGTTCCGGCAGAAGGC
CTCCATCCACGAGGCCTGGACTGACGGGAAGGAAGCCATGCTGAAGCACCGGGACTACGAGACGGCCACACTATCGGACATCAAAGCCCT
CATTCGCAAGCACGAGGCCTTCGAGAGCGACCTGGCTGCGCACCAGGACCGCGTGGAGCAGATCGCCGCCATTGCCCAGGAGCTCAACGA
GCTGGATTACTACGACTCCCACAATGTCAACACCCGGTGCCAGAAGATCTGTGACCAGTGGGACGCCCTCGGCTCTCTGACACATAGTCG
CAGGGAAGCCCTGGAGAAAACAGAGAAGCAGCTGGAGGCCATCGACCAGCTGCACCTGGAATACGCCAAGCGCGCGGCCCCCTTCAACAA
CTGGATGGAGAGCGCCATGGAGGACCTCCAGGACATGTTCATCGTCCATACCATCGAGGAGATTGAGGGCCTGATCTCAGCCCATGACCA
GTTCAAGTCCACCCTGCCGGACGCCGATAGGGAGCGCGAGGCCATCCTGGCCATCCACAAGGAGGCCCAGAGGATCGCTGAGAGCAACCA
CATCAAGCTGTCGGGCAGCAACCCCTACACCACCGTCACCCCGCAAATCATCAACTCCAAGTGGGAGAAGGTGCAGCAGCTGGTGCCAAA
ACGGGACCATGCCCTCCTGGAGGAGCAGAGCAAGCAGCAGTCCAACGAGCACCTGCGCCGCCAGTTCGCCAGCCAGGCCAATGTTGTGGG
GCCCTGGATCCAGACCAAGATGGAGGAGATCGGGCGCATCTCCATTGAGATGAACGGGACCCTGGAGGACCAGCTGAGCCACCTGAAGCA
GTATGAACGCAGCATCGTGGACTACAAGCCCAACCTGGACCTGCTGGAGCAGCAGCACCAGCTCATCCAGGAGGCCCTCATCTTCGACAA
CAAGCACACCAACTATACCATGGAGCACATCCGCGTGGGCTGGGAGCAGCTGCTCACCACCATTGCCCGCACCATCAACGAGGTGGAGAA
CCAGATCCTCACCCGCGACGCCAAGGGCATCAGCCAGGAGCAGATGCAGGAGTTCCGGGCGTCCTTCAACCACTTCGACAAGGATCATGG
CGGGGCGCTGGGGCCCGAGGAGTTCAAGGCCTGCCTCATCAGCCTGGGCTACGACGTGGAGAACGACCGGCAGGGTGAGGCCGAGTTCAA
CCGCATCATGAGCCTGGTCGACCCCAACCATAGCGGCCTTGTGACCTTCCAAGCCTTCATCGACTTCATGTCGCGGGAGACCACCGACAC
GGACACGGCTGACCAGGTCATCGCTTCCTTCAAGGTCTTAGCAGGGGACAAGAACTTCATCACAGCTGAGGAGCTGCGGAGAGAGCTGCC
CCCCGACCAGGCCGAGTACTGCATCGCCCGCATGGCGCCATACCAGGGCCCTGACGCCGTGCCCGGTGCCCTCGACTACAAGTCCTTCTC
CACGGCCTTGTATGGCGAGAGCGACCTGTGAGGCCCCAGAGACCTGACCCAACACCCCCGACGGCCTCCAGGAGGGGCCTGGGCAGCCCC
ACAGTCCCATTCCTCCACTCTGTATCTATGCAAAGCACTCTCTGCAGTCCTCCGGGGTGGGTGGGTGGGCAGGGAGGGGCTGGGGCAGGC
TCTCTCCTCTCTCTCTTTGTGGGTTGGCCAGGAGGTTCCCCCGACCAGGTTGGGGAGACTTGGGGCCAGCGCTTCTGGTCTGGTAAATAT
GTATGATGTGTTGTGCTTTTTTAACCAAGGAGGGGCCAGTGGATTCCCACAGCACAACCGGTCCCTTCCATGCCCTGGGATGCCTCACCA
CACCCAGGTCTCTTCCTTTGCTCTGAGGTCCCTTCAAGGCCTCCCCAATCCAGGCCAAAGCCCCATGTGCCTTGTCCAGGAACTGCCTGG
GCCATGCGAGGGGCCAGCAGAGGGCGCCACCACCACCTGACGGCTGGGGACCCACCCAGCCCCTCTCCCCTCTCTGCTCCAGACTCACTT
GCCATTGCCAGGAGATGGCCCCAACAAGCACCCCGCTTTTGCAGCAGAGGAGCTGAGTTGGCAGACCGGGCCCCCCTGAACCGCACCCCA
TCCCACCAGCCCCGGCCTTGCTTTGTCTGGCCTCACGTGTCTCAGATTTTCTAAGAACCAAAAAAAAAAAAGGAAAAAAAACACAAAACA
ACAAAAACCAAAAAAAAAAAAAATCACAAAAACAAAAAAACTATAAAAAAGAAAGAATTAAAAACTTTCAGAGAATTACTATTTACTTTA
TTAACTTACGGATTTATTATATAAATATATATTCACCTAGCAACATATCTCTGCCGTCTCTCCTGCTCTCATAATGAAGACATAGCCGAT
TCTCTGCCCGGGCCCCTTGCTGATGCTCCTCCGGGTCTGCGTCGGGCGTGGGTCTCTGGGGACCCTCCAGAGGTGGAGGTGGGCTGATGG
CCTGGCTGCCTGGTGGTTGATGGTTTTGCTCCCCCTACCTTTTTTTTTTGAGTTTATTCTGATTGATTTTTTTTCTTGGTTTCTGGATAA
ACCACCCTCTGGGGACAGGATAATAAAACATGTAATATTTTTAAGAAGGATTCCTGCAGCATCATCTTTTTTTATTTCTCCTGTGTCTGT
CCTCCACCTTCTAGGAGAGCCAGGGCAGAGCTAGCACTGTCTTAAGCTGTCAACGTGGACTAGCTCGTGTCATCTGCTCGAGAAGGGCTG
TCGCTGTTCTTGTTTCTGAGTGAGGAGTACGCAGGCCAGAGTGGTCACCCGGCCGTGAGCAGTGAGGGCCAGAGACTAGCCCCAGACAGG
TGGATGCCAGAGAGAGTGGCACCCATGCCAGGCAAGGCCTAGGGAGGTGGTCTTGCTCAGCAACCCTGCCCTGAGCAGCAGGTGCGCCCA
TCCGGAGATCCTAGGAGAAGGTGGCCACCTCCATCCACTAAGGAAGAGAAGGAAGACAGTGGCTTGAGGCAGGGAGCTCGCAGGACAGAG
CCTGAGCCACCCTGTCCCTCCCACCTGGCTCACCTGTCTGTGGGTCAGGCAGATGACCCCCTCACCCCCATCCAGGTGCTGGCTGCAGTG
GCCTGTGCAGAGAGGGGCAGGGTGAGTGCCCACCAGTCCCCGTACCCCTTCCCCCCATGCCCCACCATGCCGGGGTGGTACTCACAGAAG
ATGCAGGTGAGGTGGGCCACACAGGACACGAACCGCTCGAAGTCCACACGCAGACGGCTATCCCGGTAGCGGCTGGTGAGGGTCTGGGTC
AGCTGGTTGTTCAGGTGGAAGCCTAGGGGGAGGCTGCTTCTGAGCCCAGTGGCCCACAGGGAACCCACCTTGGCATTGCATCCCCACCCC
ACCTCCTCAGGGAGGACATGAATGCCACAGGGTGTCACACCCCAACTCTGCCCCATCCCGGCAGGGTGAGTACAGGCTGATCCCTTCAAT
CCTCTGGGCCTGTTTCCTCATCCATCAAACGGACTAAGACAGCCCCGACCCCATAGGGTGTGTGAAGACAGAACGCTCAGGACAGCGTCT
GACACGTGACTCGATGTGTGGGTACTGTTACTCCTTAAATCCTGTGGGGCTTTCTCCTTGCCAGTGGGCACTGGAGGATATTTCTGTGCA

>37241_37241_1_HNRNPL-ACTN4_HNRNPL_chr19_39340340_ENST00000221419_ACTN4_chr19_39205109_ENST00000252699_length(amino acids)=727AA_BP=65
MSRRLLPRAEKRRRRLEQRQQPDEQRRRSGAMVKMAAAGGGGGGGRYYGGGSEGGRAPKRLKTDNAGDQHGGGGGGGGGAGAAGGGGGGA
ETAANRICKVLAVNQENEHLMEDYEKLASDLLEWIRRTIPWLEDRVPQKTIQEMQQKLEDFRDYRRVHKPPKVQEKCQLEINFNTLQTKL
RLSNRPAFMPSEGKMVSDINNGWQHLEQAEKGYEEWLLNEIRRLERLDHLAEKFRQKASIHEAWTDGKEAMLKHRDYETATLSDIKALIR
KHEAFESDLAAHQDRVEQIAAIAQELNELDYYDSHNVNTRCQKICDQWDALGSLTHSRREALEKTEKQLEAIDQLHLEYAKRAAPFNNWM
ESAMEDLQDMFIVHTIEEIEGLISAHDQFKSTLPDADREREAILAIHKEAQRIAESNHIKLSGSNPYTTVTPQIINSKWEKVQQLVPKRD
HALLEEQSKQQSNEHLRRQFASQANVVGPWIQTKMEEIGRISIEMNGTLEDQLSHLKQYERSIVDYKPNLDLLEQQHQLIQEALIFDNKH
TNYTMEHIRVGWEQLLTTIARTINEVENQILTRDAKGISQEQMQEFRASFNHFDKDHGGALGPEEFKACLISLGYDVENDRQGEAEFNRI
MSLVDPNHSGLVTFQAFIDFMSRETTDTDTADQVIASFKVLAGDKNFITAEELRRELPPDQAEYCIARMAPYQGPDAVPGALDYKSFSTA

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

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Fusion Gene PPI Analysis for HNRNPL-ACTN4


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
TgeneACTN4chr19:39340340chr19:39205109ENST00000390009014108_12654.0693.0VCL


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with
TgeneACTN4chr19:39340340chr19:39205109ENST00000252699721108_126273.0912.0VCL
TgeneACTN4chr19:39340340chr19:39205109ENST0000025269972112_26273.0912.0VCL
TgeneACTN4chr19:39340340chr19:39205109ENST0000025269972140_61273.0912.0VCL
TgeneACTN4chr19:39340340chr19:39205109ENST0000039000901412_2654.0693.0VCL
TgeneACTN4chr19:39340340chr19:39205109ENST0000039000901440_6154.0693.0VCL


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 HNRNPL-ACTN4


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 HNRNPL-ACTN4


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