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Center for Computational Systems Medicine
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Fusion Gene and Fusion Protein Summary

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Fusion Amino Acid Sequences (multiple BPs and multiple gene isoforms)

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Fusion Protein Breakpoint Sequences - (for the Screening of the FusionNeoAntigens)

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Potential FusionNeoAntigens in HLA I - (netMHCpan v4.1 + deepHLApan v1.1)

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Potential FusionNeoAntigens in HLA II - (netMHCIIpan v4.1)

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Fusion Breakpoint 14 AA Peptide Structure - (RoseTTAFold)

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D - (Glide)

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Vaccine Design for the FusionNeoAntigens (RNA/protein sequences)

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Potential target of CAR-T therapy development

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Information on the samples that have these potential fusion neoantigens

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Fusion Protein Targeting Drugs - (Manual Curation)

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Fusion Protein Related diseases - (Manual Curation)

Fusion Protein:HSD17B12-RPS6KB1

Fusion Gene and Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: HSD17B12-RPS6KB1
FusionPDB ID: 37663
FusionGDB2.0 ID: 37663
HgeneTgene
Gene symbol

HSD17B12

RPS6KB1

Gene ID

51144

6198

Gene namehydroxysteroid 17-beta dehydrogenase 12ribosomal protein S6 kinase B1
SynonymsKAR|SDR12C1PS6K|S6K|S6K-beta-1|S6K1|STK14A|p70 S6KA|p70(S6K)-alpha|p70-S6K|p70-alpha
Cytomap

11p11.2

17q23.1

Type of geneprotein-codingprotein-coding
Descriptionvery-long-chain 3-oxoacyl-CoA reductase17-beta-HSD 1217-beta-hydroxysteroid dehydrogenase 1217beta-HSD type 123-ketoacyl-CoA reductaseestradiol 17-beta-dehydrogenase 12short chain dehydrogenase/reductase family 12C member 1steroid dehydrogenase homribosomal protein S6 kinase beta-1p70 S6 kinase, alpharibosomal protein S6 kinase Iribosomal protein S6 kinase, 70kDa, polypeptide 1serine/threonine kinase 14 alphaserine/threonine-protein kinase 14A
Modification date2020031320200313
UniProtAcc

Q53GQ0

Main function of 5'-partner protein: FUNCTION: Catalyzes the second of the four reactions of the long-chain fatty acids elongation cycle. This endoplasmic reticulum-bound enzymatic process, allows the addition of two carbons to the chain of long- and very long-chain fatty acids/VLCFAs per cycle. This enzyme has a 3-ketoacyl-CoA reductase activity, reducing 3-ketoacyl-CoA to 3-hydroxyacyl-CoA, within each cycle of fatty acid elongation. Thereby, it may participate in the production of VLCFAs of different chain lengths that are involved in multiple biological processes as precursors of membrane lipids and lipid mediators. May also catalyze the transformation of estrone (E1) into estradiol (E2) and play a role in estrogen formation. {ECO:0000269|PubMed:12482854, ECO:0000269|PubMed:16166196}.
.
Ensembl transtripts involved in fusion geneENST idsENST00000278353, ENST00000395700, 
ENST00000529261, 
ENST00000393021, 
ENST00000587061, ENST00000225577, 
ENST00000406116, ENST00000443572, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 13 X 7=118310 X 6 X 7=420
# samples 1412
** MAII scorelog2(14/1183*10)=-3.07895134139482
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(12/420*10)=-1.8073549220576
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Fusion gene context

PubMed: HSD17B12 [Title/Abstract] AND RPS6KB1 [Title/Abstract] AND fusion [Title/Abstract]

Fusion neoantigen context

PubMed: HSD17B12 [Title/Abstract] AND RPS6KB1 [Title/Abstract] AND neoantigen [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)HSD17B12(43861614)-RPS6KB1(57987923), # samples:1
Anticipated loss of major functional domain due to fusion event.HSD17B12-RPS6KB1 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.
HSD17B12-RPS6KB1 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.
HSD17B12-RPS6KB1 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.
HSD17B12-RPS6KB1 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
TgeneRPS6KB1

GO:0031667

response to nutrient levels

29750193

TgeneRPS6KB1

GO:0031929

TOR signaling

12150926

TgeneRPS6KB1

GO:0071363

cellular response to growth factor stimulus

17936702



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/chr11:43861614/chr17:57987923)
- 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 buttonRetention analysis results 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, are available here.

check buttonFusion gene breakpoints across HSD17B12 (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 RPS6KB1 (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 Amino Acid Sequences


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)
ENST00000278353HSD17B12chr1143861614+ENST00000443572RPS6KB1chr1757987923+25208031192170683
ENST00000278353HSD17B12chr1143861614+ENST00000406116RPS6KB1chr1757987923+26048031192017632
ENST00000278353HSD17B12chr1143861614+ENST00000225577RPS6KB1chr1757987923+60168031192239706

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
ENST00000278353ENST00000443572HSD17B12chr1143861614+RPS6KB1chr1757987923+0.0004816060.9995184
ENST00000278353ENST00000406116HSD17B12chr1143861614+RPS6KB1chr1757987923+0.0001828010.9998172
ENST00000278353ENST00000225577HSD17B12chr1143861614+RPS6KB1chr1757987923+0.0001138430.99988616

check button Predicted full-length fusion amino acid sequences. For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among all the predicted ones.

Get the fusion protein sequences from here.

Fusion protein sequence information is available in the fasta format.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

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Fusion Protein Breakpoint Sequences for HSD17B12-RPS6KB1

check button +/-13 AA sequence from the breakpoints of the fusion protein sequences.
HgeneHchrHbpTgeneTchrTbpLength(fusion protein)BP in fusion proteinPeptide
HSD17B12chr1143861614RPS6KB1chr1757987923803227CLHEEYRSKGVFVQGQLNESMDHGGV

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Potential FusionNeoAntigen Information of HSD17B12-RPS6KB1 in HLA I

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
HSD17B12-RPS6KB1_43861614_57987923.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCpan v4.1 (%rank<0.5) and deepHLApan v1.1 (immunogenic score>0.5)
Fusion geneHchrHbpTgeneTchrTbpHLA IFusionNeoAntigen peptideBinding scoreImmunogenic scoreNeoantigen start (at BP 13)Neoantigen end (at BP 13)
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-A30:08RSKGVFVQG0.97530.8151615
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B39:13VQGQLNESM0.33580.86421221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B13:01VQGQLNESM0.32980.89711221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B39:08VQGQLNESM0.47610.93821221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B15:05VQGQLNESM0.42640.70441221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-A30:01RSKGVFVQG0.97650.8996615
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B15:53VQGQLNESM0.86320.62211221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B15:73VQGQLNESM0.76210.66651221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B15:30VQGQLNESM0.6510.7011221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B39:02VQGQLNESM0.53220.86051221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B15:20VQGQLNESM0.41270.80181221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B48:02VQGQLNESM0.40740.79131221
HSD17B12-RPS6KB1chr1143861614chr1757987923803HLA-B35:28VQGQLNESM0.37230.83061221

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Potential FusionNeoAntigen Information of HSD17B12-RPS6KB1 in HLA II

check button Multiple sequence alignments of the potential FusionNeoAntigens per fusion breakpoints. If the MSA is empty, then it means that there were predicted fusion neoantigens in this fusion breakpoint, but those predicted fusion neoantigens were not across the breakpoint, which is not fusion-specific.
HSD17B12-RPS6KB1_43861614_57987923.msa

check button Potential FusionNeoAntigen Information
* We used NetMHCIIpan v4.1 (%rank<0.5).
Fusion geneHchrHbpTgeneTchrTbpHLA IIFusionNeoAntigen peptideNeoantigen start (at BP 13)Neoantigen end (at BP 13)
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0801LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0802LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0802HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0802CLHEEYRSKGVFVQG015
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0803LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0803HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0808LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0808HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0808CLHEEYRSKGVFVQG015
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0809LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0809HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0809CLHEEYRSKGVFVQG015
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0811LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0811HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0811CLHEEYRSKGVFVQG015
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0813LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0813HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0813CLHEEYRSKGVFVQG015
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0814LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0814HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0815LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0815HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0815CLHEEYRSKGVFVQG015
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0816LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0821LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0821HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0821CLHEEYRSKGVFVQG015
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0823LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0823HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0824LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0826LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0827LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0827HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0830LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0830HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0830CLHEEYRSKGVFVQG015
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0833LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0833HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0835LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0835HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0836LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0836HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0837LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0837HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0838LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0838HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-0839LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1130LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1130HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1145LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1145HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1164LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1347LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1347HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1367LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1367HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1403LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1427LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1427HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1440LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1467LHEEYRSKGVFVQGQ116
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1467HEEYRSKGVFVQGQL217
HSD17B12-RPS6KB1chr1143861614chr1757987923803DRB1-1477LHEEYRSKGVFVQGQ116

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Fusion breakpoint peptide structures of HSD17B12-RPS6KB1

check button3D structures of the fusion breakpoint peptide of 14AA sequence that have potential fusion neoantigens
* The minimum length of the amino acid sequence in RoseTTAFold is 14AA. Here, we predicted the 14AA fusion protein breakpoint sequence not the fusion neoantigen peptide, which is shorter than 14 AA.
File nameBPseqHgeneTgeneHchrHbpTchrTbpAAlen
8227RSKGVFVQGQLNESHSD17B12RPS6KB1chr1143861614chr1757987923803

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Filtering FusionNeoAntigens Through Checking the Interaction with HLAs in 3D of HSD17B12-RPS6KB1

check buttonVirtual screening between 25 HLAs (from PDB) and FusionNeoAntigens
* We used Glide to predict the interaction between HLAs and neoantigens.
HLA allelePDB IDFile nameBPseqDocking scoreGlide score
HLA-B14:023BVN8227RSKGVFVQGQLNES-7.15543-7.26883
HLA-B14:023BVN8227RSKGVFVQGQLNES-4.77435-5.80965
HLA-B52:013W398227RSKGVFVQGQLNES-6.80875-6.92215
HLA-B52:013W398227RSKGVFVQGQLNES-4.20386-5.23916
HLA-A11:014UQ28227RSKGVFVQGQLNES-7.5194-8.5547
HLA-A11:014UQ28227RSKGVFVQGQLNES-6.9601-7.0735
HLA-A24:025HGA8227RSKGVFVQGQLNES-7.52403-7.63743
HLA-A24:025HGA8227RSKGVFVQGQLNES-5.82433-6.85963
HLA-B27:056PYJ8227RSKGVFVQGQLNES-3.28285-4.31815
HLA-B44:053DX88227RSKGVFVQGQLNES-5.91172-6.94702
HLA-B44:053DX88227RSKGVFVQGQLNES-4.24346-4.35686

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Vaccine Design for the FusionNeoAntigens of HSD17B12-RPS6KB1

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-Is.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptide sequenceFusionNeoAntigen RNA sequence
HSD17B12-RPS6KB1chr1143861614chr17579879231221VQGQLNESMCAGGGTCAGTTAAATGAAAGCATGGAC
HSD17B12-RPS6KB1chr1143861614chr1757987923615RSKGVFVQGAGCAAGGGCGTCTTTGTGCAGGGTCAG

check button mRNA and peptide sequences of FusionNeoAntigens that have potential interaction with HLA-IIs.
Fusion geneHchrHbpTchrTbpStart in +/-13AAEnd in +/-13AAFusionNeoAntigen peptideFusionNEoAntigen RNA sequence
HSD17B12-RPS6KB1chr1143861614chr1757987923015CLHEEYRSKGVFVQGCTCCATGAGGAGTATAGGAGCAAGGGCGTCTTTGTGCAGGGTCAG
HSD17B12-RPS6KB1chr1143861614chr1757987923116LHEEYRSKGVFVQGQCATGAGGAGTATAGGAGCAAGGGCGTCTTTGTGCAGGGTCAGTTA
HSD17B12-RPS6KB1chr1143861614chr1757987923217HEEYRSKGVFVQGQLGAGGAGTATAGGAGCAAGGGCGTCTTTGTGCAGGGTCAGTTAAAT

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Information of the samples that have these potential fusion neoantigens of HSD17B12-RPS6KB1

check button These samples were reported as having these fusion breakpoints. For individual breakpoints, we checked the open reading frames considering multiple gene isoforms and chose the in-frame fusion genes only. Then, we made fusion protein sequences and predicted the fusion neoantigens. These fusion-positive samples may have these potential fusion neoantigens.
Cancer typeFusion geneHchrHbpHenstTchrTbpTenstSample
HNSCHSD17B12-RPS6KB1chr1143861614ENST00000278353chr1757987923ENST00000225577TCGA-MZ-A6I9-01A

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Potential target of CAR-T therapy development for HSD17B12-RPS6KB1

check button Predicted 3D structure. We used RoseTTAFold.

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, to provide the retention of the transmembrane domain, we only show the protein feature retention information of those transmembrane features


* Minus value of BPloci means that the break point is located before the CDS.
- In-frame and retained 'Transmembrane'.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneHSD17B12chr11:43861614chr17:57987923ENST00000278353+911182_202228313.0TransmembraneHelical
HgeneHSD17B12chr11:43861614chr17:57987923ENST00000278353+9114_24228313.0TransmembraneHelical

check button Subcellular localization prediction of the transmembrane domain retained fusion proteins
* We used DeepLoc 1.0. The order of the X-axis of the barplot is as follows: Entry_ID, Localization, Type, Nucleus, Cytoplasm, Extracellular, Mitochondrion, Cell_membrane, Endoplasmic_reticulum, Plastid, Golgi.apparatus, Lysosome.Vacuole, Peroxisome. Y-axis is the output score of DeepLoc. Clicking the image will open a new tab with a large image.
HgeneHchrHbpHenstTgeneTchrTbpTenstDeepLoc result

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Related Drugs to HSD17B12-RPS6KB1

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 HSD17B12-RPS6KB1

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