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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:HSPA5-TFAM (FusionGDB2 ID:37880)

Fusion Gene Summary for HSPA5-TFAM

check button Fusion gene summary
Fusion gene informationFusion gene name: HSPA5-TFAM
Fusion gene ID: 37880
HgeneTgene
Gene symbol

HSPA5

TFAM

Gene ID

3309

7019

Gene nameheat shock protein family A (Hsp70) member 5transcription factor A, mitochondrial
SynonymsBIP|GRP78|HEL-S-89n|MIF2MTDPS15|MTTF1|MTTFA|TCF6|TCF6L1|TCF6L2|TCF6L3
Cytomap

9q33.3

10q21.1

Type of geneprotein-codingprotein-coding
Descriptionendoplasmic reticulum chaperone BiP78 kDa glucose-regulated proteinHSP70 family protein 5binding-immunoglobulin proteinendoplasmic reticulum lumenal Ca(2+)-binding protein grp78epididymis secretory sperm binding protein Li 89nglucose-regulated protetranscription factor A, mitochondrialmitochondrial transcription factor 1mitochondrial transcription factor Atranscription factor 6transcription factor 6-like 1transcription factor 6-like 2 (mitochondrial transcription factor)transcription factor 6-
Modification date2020032720200329
UniProtAcc

P11021

.
Ensembl transtripts involved in fusion geneENST00000324460, ENST00000373895, 
ENST00000373899, ENST00000487519, 
Fusion gene scores* DoF score8 X 8 X 5=3202 X 2 X 2=8
# samples 82
** MAII scorelog2(8/320*10)=-2
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: HSPA5 [Title/Abstract] AND TFAM [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointHSPA5(128000420)-TFAM(60147950), # samples:1
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
HgeneHSPA5

GO:0042149

cellular response to glucose starvation

10085239

TgeneTFAM

GO:0006391

transcription initiation from mitochondrial promoter

20410300

TgeneTFAM

GO:0045893

positive regulation of transcription, DNA-templated

20410300


check buttonFusion gene breakpoints across HSPA5 (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 TFAM (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
ChimerDB4GBMTCGA-27-1830-01AHSPA5chr9

128000420

-TFAMchr10

60147950

+


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Fusion Gene ORF analysis for HSPA5-TFAM

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-3UTRENST00000324460ENST00000373895HSPA5chr9

128000420

-TFAMchr10

60147950

+
5CDS-3UTRENST00000324460ENST00000373899HSPA5chr9

128000420

-TFAMchr10

60147950

+
In-frameENST00000324460ENST00000487519HSPA5chr9

128000420

-TFAMchr10

60147950

+

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)
ENST00000324460HSPA5chr9128000420-ENST00000487519TFAMchr1060147950+62741606752126683

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
ENST00000324460ENST00000487519HSPA5chr9128000420-TFAMchr1060147950+9.07E-050.9999093

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Fusion Genomic Features for HSPA5-TFAM


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)
HSPA5chr9128000419-TFAMchr1060147949+0.0216864530.9783135
HSPA5chr9128000419-TFAMchr1060147949+0.0216864530.9783135

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 HSPA5-TFAM


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/chr9:128000420/chr10:60147950)
- 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
HSPA5

P11021

.
FUNCTION: Endoplasmic reticulum chaperone that plays a key role in protein folding and quality control in the endoplasmic reticulum lumen (PubMed:2294010, PubMed:23769672, PubMed:23990668, PubMed:28332555). Involved in the correct folding of proteins and degradation of misfolded proteins via its interaction with DNAJC10/ERdj5, probably to facilitate the release of DNAJC10/ERdj5 from its substrate (By similarity). Acts as a key repressor of the ERN1/IRE1-mediated unfolded protein response (UPR) (PubMed:1550958, PubMed:19538957). In the unstressed endoplasmic reticulum, recruited by DNAJB9/ERdj4 to the luminal region of ERN1/IRE1, leading to disrupt the dimerization of ERN1/IRE1, thereby inactivating ERN1/IRE1 (By similarity). Accumulation of misfolded protein in the endoplasmic reticulum causes release of HSPA5/BiP from ERN1/IRE1, allowing homodimerization and subsequent activation of ERN1/IRE1 (By similarity). Plays an auxiliary role in post-translational transport of small presecretory proteins across endoplasmic reticulum (ER). May function as an allosteric modulator for SEC61 channel-forming translocon complex, likely cooperating with SEC62 to enable the productive insertion of these precursors into SEC61 channel. Appears to specifically regulate translocation of precursors having inhibitory residues in their mature region that weaken channel gating. May also play a role in apoptosis and cell proliferation (PubMed:26045166). {ECO:0000250|UniProtKB:G3I8R9, ECO:0000250|UniProtKB:P20029, ECO:0000269|PubMed:1550958, ECO:0000269|PubMed:19538957, ECO:0000269|PubMed:2294010, ECO:0000269|PubMed:23769672, ECO:0000269|PubMed:23990668, ECO:0000269|PubMed:26045166, ECO:0000269|PubMed:28332555, ECO:0000269|PubMed:29719251}.FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.

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
HgeneHSPA5chr9:128000420chr10:60147950ENST00000324460-78227_229467655.0Nucleotide bindingATP
HgeneHSPA5chr9:128000420chr10:60147950ENST00000324460-78293_300467655.0Nucleotide bindingATP
HgeneHSPA5chr9:128000420chr10:60147950ENST00000324460-7836_39467655.0Nucleotide bindingATP
HgeneHSPA5chr9:128000420chr10:60147950ENST00000324460-78125_280467655.0RegionNucleotide-binding (NBD)
HgeneHSPA5chr9:128000420chr10:60147950ENST00000324460-78409_419467655.0RegionInterdomain linker
TgeneTFAMchr9:128000420chr10:60147950ENST0000037389516155_21973215.0DNA bindingHMG box 2
TgeneTFAMchr9:128000420chr10:60147950ENST0000048751917155_21973247.0DNA bindingHMG box 2

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneHSPA5chr9:128000420chr10:60147950ENST00000324460-78651_654467655.0MotifPrevents secretion from ER
HgeneHSPA5chr9:128000420chr10:60147950ENST00000324460-78420_500467655.0RegionSubstrate-binding (SBD)
TgeneTFAMchr9:128000420chr10:60147950ENST000003738951650_11873215.0DNA bindingHMG box 1
TgeneTFAMchr9:128000420chr10:60147950ENST000004875191750_11873247.0DNA bindingHMG box 1


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Fusion Gene Sequence for HSPA5-TFAM


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.
>37880_37880_1_HSPA5-TFAM_HSPA5_chr9_128000420_ENST00000324460_TFAM_chr10_60147950_ENST00000487519_length(transcript)=6274nt_BP=1606nt
ACAGCACAGACAGATTGACCTATTGGGGTGTTTCGCGAGTGTGAGAGGGAAGCGCCGCGGCCTGTATTTCTAGACCTGCCCTTCGCCTGG
TTCGTGGCGCCTTGTGACCCCGGGCCCCTGCCGCCTGCAAGTCGGAAATTGCGCTGTGCTCCTGTGCTACGGCCTGTGGCTGGACTGCCT
GCTGCTGCCCAACTGGCTGGCAAGATGAAGCTCTCCCTGGTGGCCGCGATGCTGCTGCTGCTCAGCGCGGCGCGGGCCGAGGAGGAGGAC
AAGAAGGAGGACGTGGGCACGGTGGTCGGCATCGACCTGGGGACCACCTACTCCTGCGTCGGCGTGTTCAAGAACGGCCGCGTGGAGATC
ATCGCCAACGATCAGGGCAACCGCATCACGCCGTCCTATGTCGCCTTCACTCCTGAAGGGGAACGTCTGATTGGCGATGCCGCCAAGAAC
CAGCTCACCTCCAACCCCGAGAACACGGTCTTTGACGCCAAGCGGCTCATCGGCCGCACGTGGAATGACCCGTCTGTGCAGCAGGACATC
AAGTTCTTGCCGTTCAAGGTGGTTGAAAAGAAAACTAAACCATACATTCAAGTTGATATTGGAGGTGGGCAAACAAAGACATTTGCTCCT
GAAGAAATTTCTGCCATGGTTCTCACTAAAATGAAAGAAACCGCTGAGGCTTATTTGGGAAAGAAGGTTACCCATGCAGTTGTTACTGTA
CCAGCCTATTTTAATGATGCCCAACGCCAAGCAACCAAAGACGCTGGAACTATTGCTGGCCTAAATGTTATGAGGATCATCAACGAGCCT
ACGGCAGCTGCTATTGCTTATGGCCTGGATAAGAGGGAGGGGGAGAAGAACATCCTGGTGTTTGACCTGGGTGGCGGAACCTTCGATGTG
TCTCTTCTCACCATTGACAATGGTGTCTTCGAAGTTGTGGCCACTAATGGAGATACTCATCTGGGTGGAGAAGACTTTGACCAGCGTGTC
ATGGAACACTTCATCAAACTGTACAAAAAGAAGACGGGCAAAGATGTCAGGAAAGACAATAGAGCTGTGCAGAAACTCCGGCGCGAGGTA
GAAAAGGCCAAACGGGCCCTGTCTTCTCAGCATCAAGCAAGAATTGAAATTGAGTCCTTCTATGAAGGAGAAGACTTTTCTGAGACCCTG
ACTCGGGCCAAATTTGAAGAGCTCAACATGGATCTGTTCCGGTCTACTATGAAGCCCGTCCAGAAAGTGTTGGAAGATTCTGATTTGAAG
AAGTCTGATATTGATGAAATTGTTCTTGTTGGTGGCTCGACTCGAATTCCAAAGATTCAGCAACTGGTTAAAGAGTTCTTCAATGGCAAG
GAACCATCCCGTGGCATAAACCCAGATGAAGCTGTAGCGTATGGTGCTGCTGTCCAGGCTGGTGTGCTCTCTGGTGATCAAGATACAGGT
GACCTGGTACTGCTTGATGTATGTCCCCTTACACTTGGTATTGAAACTGTGGGAGGTGTCATGACCAAACTGATTCCAAGGAACACAGTG
GTGCCTACCAAGAAGTCTCAGATCTTTTCTACAGCTTCTGATAATCAACCAACTGTTACAATCAAGGTCTATGAAGATGCAAAAACTACA
GAACTAATTAGAAGAATTGCCCAGCGTTGGAGGGAACTTCCTGATTCAAAGAAAAAAATATATCAAGATGCTTATAGGGCGGAGTGGCAG
GTATATAAAGAAGAGATAAGCAGATTTAAAGAACAGCTAACTCCAAGTCAGATTATGTCTTTGGAAAAAGAAATCATGGACAAACATTTA
AAAAGGAAAGCTATGACAAAAAAAAAAGAGTTAACACTGCTTGGAAAACCAAAAAGACCTCGTTCAGCTTATAACGTTTATGTAGCTGAA
AGATTCCAAGAAGCTAAGGGTGATTCACCGCAGGAAAAGCTGAAGACTGTAAAGGAAAACTGGAAAAATCTGTCTGACTCTGAAAAGGAA
TTATATATTCAGCATGCTAAAGAGGACGAAACTCGTTATCATAATGAAATGAAGTCTTGGGAAGAACAAATGATTGAAGTTGGACGAAAG
GATCTTCTACGTCGCACAATAAAGAAACAACGAAAATATGGTGCTGAGGAGTGTTAAAAGTAGAAGATTGAGATGTGTTCACAATGGATA
GGCACAGGAAACCAGTTAGGTCTCAATACCTGAAGCTATCGTAAAATTAAGAAAGGATAAAGTTGGTAAACCTTTTATATTTAGTATCTT
TTTATTCAGCTCATGGACTTCTGCCAGCATAATACTTGCTTTGGAAAACCCAGATAAAGGTTCATGCAAACTTTATTTTGTGTTTAGGAA
CTACTGAGGATCAGAGTAATCCAAGCAAATGTGAATCATTTTACCTTTGACAAAGGTAAATCAGACTATGAAGTTTTTTTTATACAGGAT
GATGACTATGGAAAGAGTACTCTTGTTTCCTTATATTATGGAGGCAGGAGTTTCGTTTTCAAAATTGTTACAAATTGTAGAAGCCACGGT
GTTCTGTGATATAAGTGTGTGTTTTTCATAAAGCAGGCAGAACTCATCTAGGTAAATTACAGTTCCTAGGTATAATTCACATTGTATTCA
GAGTTGATGGTTGTACATATAAGTGATTGCTGGTTTTAGTTGCAACTTTGTATAAAAGGGACTGAGAAATTTATAAACTTTTTTCTTACT
GTCTTTTTTCTAAAGTAAAAACAAAGAAATTATGTGCCAGATTTATGCATATTATTTTATGTTGCATAGAATAAAATTTTTAATCTTTAA
TTTTACATTTCCTAAATATATTTTAAGACGAAACATTTGTTCTATAGCTTTTCCCTTTTTTTAAGTAAGGAATTTTATTTTTTTCTGAAT
TATTTTCTCTCGTGAGTATATTGATCCAGAAAGAAAACTTGTATTATGTGTGTTTTAAAATGAGAAATCTAAAAAACGAAAAGTCTCCAA
AGTCTCTGGAATTTGAAACACTTTGCATAACGTATAAAAGCCTGTTTAAGAGACAGCCAACTATGGCCTGTGGATCAAATCCAGCCTGCT
GCCTGCTTTTTATGGCCTGTGAGCTAGGAATTGTGTTTATAATTTTAAATGTTTTTTTTTAAAGACTTTTATGATACTTGAAAATTAACA
TGAATATTTAGTGTTCATAAATAAAGTTTGTTGAAACACAACCAAGATCATTCTTTTACTTGTCTATGGCTGCTTTTCTGTGGCAGAGTA
GCTGCCACAGAAACTATAGCCCACAAAGCCTGATATTTACTGTCTGTCTGTTTATGGAAAAAATTTATCAACCCATGGTCTATAGTATAG
TGTGATATGACTACTGTTCCAATGTATTGAAGTGTTGGGATAGTTTTTTCAAATGTTTTCAGATGTTCTTGTTTTAGAATCATTGTCACC
TTTAAGAGGAAAAAGGTCATCACTAGATAATCTAAACAAATTGTTGCTTCTCAGTGTTAGCAAGGAAAATAATCTAGTTTCAAATTACAT
TGCAGTATAATGAAAAAGATCCATATACTGTGGAATGATATTCTTTTAAAATTATTTGCTATGGCTTGGTAAAAATGTACTTTTTCCAGT
AGCACATATCACAAGAACCTCACTGTAGTTGAAAGCCATCTTTCTTTAGTATTTGTTTATCCTTTTAGGAGAGTCAAGCAAAGGTTTTCA
CCACCTGTTTGAGCAGAATAATTCTCATCAGTTCACAGATATAGGATAACTCAATTTATATGCACTTTATGCGTTATGCAAAATATTTAG
AAATTGTAGATTCTAGATCTCCAGAAAGACTTTGAAGACTTTGATGTCACAAAAAGATGACTTGTTATATGCTGAGCTTGACAAAGGTAG
GAATGGGAGAGAAAAATAGTAGCTTATGAGGAAATATGAGGCTTTAAATATATAAAGTTGGATATTTTAAAATAACTTTTCCCTGTGGGA
GCTTCTCACTCTGGGTGCAGACAGGACAGTGTTGGCCATTGGTGAAATAGATAGGATGGGTTTGAGGCCAGAGCAGTCTGGGAGTAGGGG
GAAAGAGAAGGAGGTGTGCTAGTGTCTATCACAGGCTTTCTCAATTAGGTTTGCAGGAGAAAAAGCCCTAAGTCCCTGTGTCATCTAGAA
TGGTACTAATTATGTACAGTCCCTAGGAGAATGGAGAAAATCATAACTCAAATCATCGACTCAATTCTGTTCTCTTCAGATGAGCTCAGA
GAGCACATAGGAGTGTTTGTAATGAGGGGTATGTAATGATTGAGATAGAGGAATGAGTTACATAAACATCTCGGGACAAATGCAGCATAG
AAAACATCTTTGTAGTTACCCTGCGGGGAAATTTCCTCTGAGTTCTTTTAACATTAACTACCCGTATTATTTTATACTTAACATTCATAT
CATACCTTCCCAAATATATTGGGAAGTTCAGTGTTAAGTACGTTTCTCAAGTACTTAACAACTTAATATAGGGAGGAAAGGTGTAAACAG
TGAAAAAAGAGCAAAACTATTTTATGGTAATTTTATGGTAGTATCAGCTTGTATTTGGTTCTCTGTTTCTAAAATAATGTAATTTTTAAT
ATTTTAAATAATAGGATAACCTGGTTTCCAAGCCTTTTTTTCCCCCGACATCCAGAATACACACTGGATCCAAGCCTTTCTTAAACATCA
GTACATGTGGAAGACTGGCATGCCATATACCAAATGCCATTCAGCTGTAACAGTATACACAGATTTTCTCTTATAAAGAATAAGAACATC
ATAACCAATGACCACTCATATAAAGTCTTATTTGTGTGTGTGTGTGTGTGTGTGTGCACGTGTGTGTGTTAGAGTCTCATTATATTGCTC
AGGCTGGAGGGCATGGTGTGATCTTGGCTCACTGCAGCCTTGACCTCCTGGGCTCAAGTGATCCTTCCGAGTCGTTGGGACTACAGTAGG
TGAACACCACCATGCCTGGCTAATTTTTGTATTTTTTTTTTAATCAAGATGGGATCTTGCTATGTTGCCCAGGCTGGTCTCAAACTCCTG
GCATCAAGCGTTCCTCCTTCCTTGGCCTCCTTAAGTGCTGGGATTATAGGTGTGAGCCACCATGCTTGACCATAAAGCCTTACTATTTCT
TTTGGAGACACAGTCTTGCTCTGTCCAAGCTGGAATGCAGTGATGTGATCATGGCTCACTGCAGCCTTGAACTCCCAGGCTTAAGAGATC
CTCCCATCTCAGCCTCCTGAGTAGCTGGGATTATAGGTGCAGACCATCAAGCCTTGCTATTATTTTTTAGACTTTTCTTAATTTCATCCA
ACAAAGTAGTTGCTGTAGGAGCTGAGTGTTAGAAGGAAAGATGCTGAAGAAATGAAATCAAGCAGGGTGTATACTGTCATGAATAGGCAT
ACAGTAGTTTTTATACTTTTGTTCTTTGGAGTACCAATGTTAGGTTTTACAAAAGTAATTTGATGAGGGGAAGGAGGGTTGTGTATTTAT
TTTACTTTCTGATGTTTGCTTAAATAATACTGTGTACGTATTCAGCTTGCTGTAATTCTGTAATTACGCTATTGCGTTTGGCTAACTCCT
TTTTGGAAATGTCTTTTTTTTTGTACAAGGCATGTGTTAGTTTTTACTAATTGCTCTGAATGTGTATATTTAGATTTCTGAATTGAAAAA
AAATAGCGTACAATAAGTAGATTTAAAGTAATTAGAACACTTTATTGATTTTTCTGATGTTTTCTGTATCTAAAATTTATCACCACCAGG
TTGTGCTAAAACAGCAGGAAGTTTTTATATTGTGAGTGACAGTACCCATTATTTCTCTTAATTTTACTAACATTTACTATAAGAATATTC
TCTCGCTCTTTTCTCCACTCACAGCCATTCTCCCTCCTTCTCTTCATAACATCAAGCTGTCACAGACAAATCTGAAAATGTTACAAGCAC
AGACTATGTTGTATGTTTTGAAATTTTAGAACAGTAATGTTCTTTTTAAAATTGAACTTCTGCAGAGTAAGAAAATGAATACATTTATTA
CTTTAAATTTGTAAAATTTTCCAAAGTAAAACCATACAAAGCTAGTGTCAGTCTCTCTCATTGTTCACAAATAAAGGACTTTTGTTAATT
GATTAAATCACTTACTATATTCGATATGAAATATATAAAACATACAACCATTATCTAATACATTTCAGAATGTTTCACTGGTTACAGGAG

>37880_37880_1_HSPA5-TFAM_HSPA5_chr9_128000420_ENST00000324460_TFAM_chr10_60147950_ENST00000487519_length(amino acids)=683AA_BP=510
MPFAWFVAPCDPGPLPPASRKLRCAPVLRPVAGLPAAAQLAGKMKLSLVAAMLLLLSAARAEEEDKKEDVGTVVGIDLGTTYSCVGVFKN
GRVEIIANDQGNRITPSYVAFTPEGERLIGDAAKNQLTSNPENTVFDAKRLIGRTWNDPSVQQDIKFLPFKVVEKKTKPYIQVDIGGGQT
KTFAPEEISAMVLTKMKETAEAYLGKKVTHAVVTVPAYFNDAQRQATKDAGTIAGLNVMRIINEPTAAAIAYGLDKREGEKNILVFDLGG
GTFDVSLLTIDNGVFEVVATNGDTHLGGEDFDQRVMEHFIKLYKKKTGKDVRKDNRAVQKLRREVEKAKRALSSQHQARIEIESFYEGED
FSETLTRAKFEELNMDLFRSTMKPVQKVLEDSDLKKSDIDEIVLVGGSTRIPKIQQLVKEFFNGKEPSRGINPDEAVAYGAAVQAGVLSG
DQDTGDLVLLDVCPLTLGIETVGGVMTKLIPRNTVVPTKKSQIFSTASDNQPTVTIKVYEDAKTTELIRRIAQRWRELPDSKKKIYQDAY
RAEWQVYKEEISRFKEQLTPSQIMSLEKEIMDKHLKRKAMTKKKELTLLGKPKRPRSAYNVYVAERFQEAKGDSPQEKLKTVKENWKNLS

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

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Fusion Gene PPI Analysis for HSPA5-TFAM


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


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 HSPA5-TFAM


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 HSPA5-TFAM


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