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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:MBTD1-CLTC

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MBTD1-CLTC
FusionPDB ID: 52092
FusionGDB2.0 ID: 52092
HgeneTgene
Gene symbol

MBTD1

CLTC

Gene ID

54799

1213

Gene namembt domain containing 1clathrin heavy chain
SynonymsSA49P01CHC|CHC17|CLH-17|CLTCL2|Hc|MRD56
Cytomap

17q21.33

17q23.1

Type of geneprotein-codingprotein-coding
DescriptionMBT domain-containing protein 1clathrin heavy chain 1clathrin heavy chain on chromosome 17clathrin, heavy polypeptide (Hc)clathrin, heavy polypeptide-like 2
Modification date2020031320200313
UniProtAcc

Q05BQ5

P53675

Ensembl transtripts involved in fusion geneENST idsENST00000376381, ENST00000415868, 
ENST00000586178, ENST00000593259, 
ENST00000579815, ENST00000579456, 
ENST00000269122, ENST00000393043, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score13 X 12 X 11=171618 X 18 X 8=2592
# samples 1722
** MAII scorelog2(17/1716*10)=-3.33544290136184
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(22/2592*10)=-3.55849028935997
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: MBTD1 [Title/Abstract] AND CLTC [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MBTD1(49281152)-CLTC(57752062), # samples:1
Anticipated loss of major functional domain due to fusion event.MBTD1-CLTC 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.
MBTD1-CLTC 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.
MBTD1-CLTC 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.
MBTD1-CLTC 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.
MBTD1-CLTC seems lost the major protein functional domain in Hgene partner, which is a epigenetic factor due to the frame-shifted ORF.
MBTD1-CLTC seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
MBTD1-CLTC seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
MBTD1-CLTC seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted 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
TgeneCLTC

GO:1900126

negative regulation of hyaluronan biosynthetic process

24251095


check buttonFusion gene breakpoints across MBTD1 (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 CLTC (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
ChimerDB4Non-CancerERR315481MBTD1chr17

49281152

-CLTCchr17

57752062

+


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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)
ENST00000586178MBTD1chr1749281152-ENST00000393043CLTCchr1757752062+368310839693584871
ENST00000586178MBTD1chr1749281152-ENST00000269122CLTCchr1757752062+615110839693692907

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
ENST00000586178ENST00000393043MBTD1chr1749281152-CLTCchr1757752062+0.0019773040.9980227
ENST00000586178ENST00000269122MBTD1chr1749281152-CLTCchr1757752062+0.0006757210.9993243

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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

>52092_52092_1_MBTD1-CLTC_MBTD1_chr17_49281152_ENST00000586178_CLTC_chr17_57752062_ENST00000269122_length(amino acids)=907AA_BP=38
MKDLKMTLVWTSGAIYVVLISIQLVGVQPAENLLFLLEVNPSRLPVVIGGLLDVDCSEDVIKNLILVVRGQFSTDELVAEVEKRNRLKLL
LPWLEARIHEGCEEPATHNALAKIYIDSNNNPERFLRENPYYDSRVVGKYCEKRDPHLACVAYERGQCDLELINVCNENSLFKSLSRYLV
RRKDPELWGSVLLESNPYRRPLIDQVVQTALSETQDPEEVSVTVKAFMTADLPNELIELLEKIVLDNSVFSEHRNLQNLLILTAIKADRT
RVMEYINRLDNYDAPDIANIAISNELFEEAFAIFRKFDVNTSAVQVLIEHIGNLDRAYEFAERCNEPAVWSQLAKAQLQKGMVKEAIDSY
IKADDPSSYMEVVQAANTSGNWEELVKYLQMARKKARESYVETELIFALAKTNRLAELEEFINGPNNAHIQQVGDRCYDEKMYDAAKLLY
NNVSNFGRLASTLVHLGEYQAAVDGARKANSTRTWKEVCFACVDGKEFRLAQMCGLHIVVHADELEELINYYQDRGYFEELITMLEAALG
LERAHMGMFTELAILYSKFKPQKMREHLELFWSRVNIPKVLRAAEQAHLWAELVFLYDKYEEYDNAIITMMNHPTDAWKEGQFKDIITKV
ANVELYYRAIQFYLEFKPLLLNDLLMVLSPRLDHTRAVNYFSKVKQLPLVKPYLRSVQNHNNKSVNESLNNLFITEEDYQALRTSIDAYD
NFDNISLAQRLEKHELIEFRRIAAYLFKGNNRWKQSVELCKKDSLYKDAMQYASESKDTELAEELLQWFLQEEKRECFGACLFTCYDLLR
PDVVLETAWRHNIMDFAMPYFIQVMKEYLTKVDKLDASESLRKEEEQATETQPIVYGQPQLMLTAGPSVAVPPQAPFGYGYTAPPYGQPQ

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>52092_52092_2_MBTD1-CLTC_MBTD1_chr17_49281152_ENST00000586178_CLTC_chr17_57752062_ENST00000393043_length(amino acids)=871AA_BP=38
MKDLKMTLVWTSGAIYVVLISIQLVGVQPAENLLFLLEVNPSRLPVVIGGLLDVDCSEDVIKNLILVVRGQFSTDELVAEVEKRNRLKLL
LPWLEARIHEGCEEPATHNALAKIYIDSNNNPERFLRENPYYDSRVVGKYCEKRDPHLACVAYERGQCDLELINVCNENSLFKSLSRYLV
RRKDPELWGSVLLESNPYRRPLIDQVVQTALSETQDPEEVSVTVKAFMTADLPNELIELLEKIVLDNSVFSEHRNLQNLLILTAIKADRT
RVMEYINRLDNYDAPDIANIAISNELFEEAFAIFRKFDVNTSAVQVLIEHIGNLDRAYEFAERCNEPAVWSQLAKAQLQKGMVKEAIDSY
IKADDPSSYMEVVQAANTSGNWEELVKYLQMARKKARESYVETELIFALAKTNRLAELEEFINGPNNAHIQQVGDRCYDEKMYDAAKLLY
NNVSNFGRLASTLVHLGEYQAAVDGARKANSTRTWKEVCFACVDGKEFRLAQMCGLHIVVHADELEELINYYQDRGYFEELITMLEAALG
LERAHMGMFTELAILYSKFKPQKMREHLELFWSRVNIPKVLRAAEQAHLWAELVFLYDKYEEYDNAIITMMNHPTDAWKEGQFKDIITKV
ANVELYYRAIQFYLEFKPLLLNDLLMVLSPRLDHTRAVNYFSKVKQLPLVKPYLRSVQNHNNKSVNESLNNLFITEEDYQALRTSIDAYD
NFDNISLAQRLEKHELIEFRRIAAYLFKGNNRWKQSVELCKKDSLYKDAMQYASESKDTELAEELLQWFLQEEKRECFGACLFTCYDLLR

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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/chr17:49281152/chr17:57752062)
- 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
MBTD1

Q05BQ5

CLTC

P53675

FUNCTION: Putative Polycomb group (PcG) protein. PcG proteins maintain the transcriptionally repressive state of genes, probably via a modification of chromatin, rendering it heritably changed in its expressibility (By similarity). Specifically binds to monomethylated and dimethylated 'Lys-20' on histone H4. {ECO:0000250, ECO:0000269|PubMed:19841675}.FUNCTION: Clathrin is the major protein of the polyhedral coat of coated pits and vesicles. Two different adapter protein complexes link the clathrin lattice either to the plasma membrane or to the trans-Golgi network (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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMBTD1chr17:49281152chr17:57752062ENST00000376381-815141_245246.33333333333334390.0RepeatNote=MBT 1
HgeneMBTD1chr17:49281152chr17:57752062ENST00000415868-615141_245246.33333333333334629.0RepeatNote=MBT 1
HgeneMBTD1chr17:49281152chr17:57752062ENST00000586178-817141_245246.33333333333334629.0RepeatNote=MBT 1
HgeneMBTD1chr17:49281152chr17:57752062ENST00000376381-81545_80246.33333333333334390.0Zinc fingerFCS-type
HgeneMBTD1chr17:49281152chr17:57752062ENST00000415868-61545_80246.33333333333334629.0Zinc fingerFCS-type
HgeneMBTD1chr17:49281152chr17:57752062ENST00000586178-81745_80246.33333333333334629.0Zinc fingerFCS-type
TgeneCLTCchr17:49281152chr17:57752062ENST0000026912214321213_1522806.01676.0RegionInvolved in binding clathrin light chain
TgeneCLTCchr17:49281152chr17:57752062ENST0000026912214321550_1675806.01676.0RegionTrimerization
TgeneCLTCchr17:49281152chr17:57752062ENST0000039304314311213_1522806.01640.0RegionInvolved in binding clathrin light chain
TgeneCLTCchr17:49281152chr17:57752062ENST0000039304314311550_1675806.01640.0RegionTrimerization
TgeneCLTCchr17:49281152chr17:57752062ENST0000026912214321128_1269806.01676.0RepeatCHCR 5
TgeneCLTCchr17:49281152chr17:57752062ENST0000026912214321274_1420806.01676.0RepeatCHCR 6
TgeneCLTCchr17:49281152chr17:57752062ENST0000026912214321423_1566806.01676.0RepeatCHCR 7
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432833_972806.01676.0RepeatCHCR 3
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432979_1124806.01676.0RepeatCHCR 4
TgeneCLTCchr17:49281152chr17:57752062ENST0000039304314311128_1269806.01640.0RepeatCHCR 5
TgeneCLTCchr17:49281152chr17:57752062ENST0000039304314311274_1420806.01640.0RepeatCHCR 6
TgeneCLTCchr17:49281152chr17:57752062ENST0000039304314311423_1566806.01640.0RepeatCHCR 7
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431833_972806.01640.0RepeatCHCR 3
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431979_1124806.01640.0RepeatCHCR 4

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMBTD1chr17:49281152chr17:57752062ENST00000376381-815253_350246.33333333333334390.0RepeatNote=MBT 2
HgeneMBTD1chr17:49281152chr17:57752062ENST00000376381-815351_456246.33333333333334390.0RepeatNote=MBT 3
HgeneMBTD1chr17:49281152chr17:57752062ENST00000376381-815464_560246.33333333333334390.0RepeatNote=MBT 4
HgeneMBTD1chr17:49281152chr17:57752062ENST00000415868-615253_350246.33333333333334629.0RepeatNote=MBT 2
HgeneMBTD1chr17:49281152chr17:57752062ENST00000415868-615351_456246.33333333333334629.0RepeatNote=MBT 3
HgeneMBTD1chr17:49281152chr17:57752062ENST00000415868-615464_560246.33333333333334629.0RepeatNote=MBT 4
HgeneMBTD1chr17:49281152chr17:57752062ENST00000586178-817253_350246.33333333333334629.0RepeatNote=MBT 2
HgeneMBTD1chr17:49281152chr17:57752062ENST00000586178-817351_456246.33333333333334629.0RepeatNote=MBT 3
HgeneMBTD1chr17:49281152chr17:57752062ENST00000586178-817464_560246.33333333333334629.0RepeatNote=MBT 4
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432108_149806.01676.0RegionNote=WD40-like repeat 3
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432150_195806.01676.0RegionNote=WD40-like repeat 4
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432196_257806.01676.0RegionNote=WD40-like repeat 5
TgeneCLTCchr17:49281152chr17:57752062ENST00000269122143224_67806.01676.0RegionNote=WD40-like repeat 1
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432258_301806.01676.0RegionNote=WD40-like repeat 6
TgeneCLTCchr17:49281152chr17:57752062ENST0000026912214322_479806.01676.0RegionNote=Globular terminal domain
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432302_330806.01676.0RegionNote=WD40-like repeat 7
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432449_465806.01676.0RegionBinding site for the uncoating ATPase%2C involved in lattice disassembly
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432480_523806.01676.0RegionNote=Flexible linker
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432524_1675806.01676.0RegionNote=Heavy chain arm
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432524_634806.01676.0RegionNote=Distal segment
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432639_1675806.01676.0RegionNote=Proximal segment
TgeneCLTCchr17:49281152chr17:57752062ENST00000269122143268_107806.01676.0RegionNote=WD40-like repeat 2
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431108_149806.01640.0RegionNote=WD40-like repeat 3
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431150_195806.01640.0RegionNote=WD40-like repeat 4
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431196_257806.01640.0RegionNote=WD40-like repeat 5
TgeneCLTCchr17:49281152chr17:57752062ENST00000393043143124_67806.01640.0RegionNote=WD40-like repeat 1
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431258_301806.01640.0RegionNote=WD40-like repeat 6
TgeneCLTCchr17:49281152chr17:57752062ENST0000039304314312_479806.01640.0RegionNote=Globular terminal domain
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431302_330806.01640.0RegionNote=WD40-like repeat 7
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431449_465806.01640.0RegionBinding site for the uncoating ATPase%2C involved in lattice disassembly
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431480_523806.01640.0RegionNote=Flexible linker
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431524_1675806.01640.0RegionNote=Heavy chain arm
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431524_634806.01640.0RegionNote=Distal segment
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431639_1675806.01640.0RegionNote=Proximal segment
TgeneCLTCchr17:49281152chr17:57752062ENST00000393043143168_107806.01640.0RegionNote=WD40-like repeat 2
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432537_683806.01676.0RepeatCHCR 1
TgeneCLTCchr17:49281152chr17:57752062ENST000002691221432686_828806.01676.0RepeatCHCR 2
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431537_683806.01640.0RepeatCHCR 1
TgeneCLTCchr17:49281152chr17:57752062ENST000003930431431686_828806.01640.0RepeatCHCR 2


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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
CLTCHGS, MCC, IKBKE, TFE3, SNX5, TOM1, SNX9, DNAJC6, ARMCX3, C10orf88, EPN1, EHD1, GGA1, GGA2, GGA3, KIT, AMPH, CLINT1, TNK2, LDLRAP1, HIP1, AP1B1, AP2A2, AP3B2, MAP3K10, PICALM, EPN2, Epn1, VCL, Arrb2, STAMBP, STAMBPL1, STAM, MAP1LC3A, SNCA, PRKACA, WNK1, Mapk13, HDAC5, SPG20, RICTOR, Erh, Cd2ap, Pttg1, EBNA-LP, PCM1, NDRG1, PPP1CA, ITSN1, ARRB1, SIRT7, SH3KBP1, DYRK1A, SNAP91, AP2B1, BIN1, AP1G1, RAC1, TOM1L1, TOM1L2, ISG15, CUL3, CUL5, CUL2, CDK2, CUL1, COPS5, DCUN1D1, CAND1, NEDD8, XRCC6, HERC1, ATG16L1, SYNJ1, LRRK2, Nfe2l2, AKT1, GRB2, SHC1, AP2M1, MYO6, SRC, FYN, Htt, DNAJA3, RPSA, ESR1, PAXIP1, PPP1CC, SMURF1, ARRB2, ERBB2, FN1, VCAM1, Fcho2, DAB2, UBL4A, ITGA4, MYBL2, SVIL, PAN2, NPM1, PTAFR, ATP4A, EP300, QARS, YWHAQ, FBXO6, RPA1, RPA2, RPA3, ERG, EPHA2, LGR4, Fbxl16, STAU1, TP53, HUWE1, FBXW11, GJB5, NXF1, ADRB2, AVPR2, CUL7, OBSL1, CCDC8, EED, ZFYVE9, OCRL, ATR, SCYL2, HTR6, HNRNPA1, UNK, ATP1A1, ATP1A2, ATP1A3, ATP5C1, CCDC47, CCT3, CCT6A, BLOC1S1, CAD, CANX, CCT6B, CISD1, CLTA, CYC1, DHX38, EHD2, FASTKD2, HSP90B1, IPO5, MTCH2, NDUFB9, NDUFS1, NLRP1, RAB5B, RANBP2, RANBP6, SLC25A3, SSR3, TECR, TOMM22, UQCRC2, VDAC1, VDAC2, VDAC3, ZMPSTE24, DDOST, EIF6, COX2, PHB, PHB2, PPP2R1A, PPP2R1B, RPN1, TMCO1, TUFM, UQCRQ, NTRK1, OFD1, CEP97, CNTRL, FBF1, NPHP1, DCTN1, POC5, POC1B, PPME1, ABCA2, PARP4, AP2A1, ATP6V1B2, ATP6V0A1, CAV1, CLTB, CAPZA2, DBN1, FLNA, GAK, MYH9, DNAJC7, IQGAP1, PDLIM7, SEC16A, SYNPO, MAPRE1, LIMA1, GTSE1, ANLN, MYO19, ARX, MYO18A, CSNK1A1, CSNK1E, STOM, EPS15, HSPA1A, HSPA4, NDUFA9, CHMP1A, PIK3C2A, PRKAR2A, SEC13, SOAT1, CLTCL1, SORBS2, PKP4, USO1, NUMB, TNK1, RAB11A, HIP1R, ATP6V0D1, XPR1, SEC24C, KIAA0430, IST1, HELZ, MVP, TROAP, SEC24B, RBM14, SEC23A, VTI1B, TRAFD1, PKP3, AAK1, BTBD3, TNRC6B, EDC4, DSTYK, PTPN23, NECAP1, TNRC6A, EHD4, EGFL7, ATP6V1D, PTRH2, PLEKHA5, CPVL, BMP2K, DCP1A, ERBB2IP, CHMP1B, KIDINS220, MTUS1, DENND1A, CRTC3, CPSF7, EDC3, CCDC115, FAM83A, REPS1, STON2, FCHO2, CHMP4B, MITD1, CRTC2, FAM83B, FAM83H, SLC35B2, Actb, Myh9, Myo1c, Ppp1cb, Tpm1, Coro1c, Cul3, Spast, Tmod3, Dctn3, Uso1, Lima1, Samm50, Calml3, Myh10, Strn3, Smap1, Ptpn23, Nhsl1, Sec24c, Flnb, IKBKB, MAP3K7, MCM2, AP3D1, U2AF2, CDC73, ZNF746, ARF6, CYLD, LASP1, BRCA1, TES, MTF1, BRD1, CFTR, ZNF598, PDGFRB, FBXO7, TMPO, PTCH1, HSPA8, MAP2K1, PIK3CA, APOE, BMPR1A, JUP, UQCRB, UBE2M, RAD18, PRPF8, EFTUD2, AAR2, PIH1D1, TNIP2, LARP7, RNF4, TNF, SPDL1, RIOK1, PRKCZ, HEXIM1, MEPCE, RUNX1, RNF123, PPT1, HERC2, UBE3A, AGR2, RECQL4, SMAP1, MYC, CDK9, Prkaa1, Prkab1, CDK5RAP2, GRWD1, KRT17, KIAA1429, PLEKHA2, RC3H2, ACTC1, TET2, NR2C2, UCHL3, PRDM16, MECOM, AGRN, BMH1, BMH2, ATXN3, TCF7L2, STX2, GSK3B, ABCC6, BIRC3, LMBR1L, WWP2, Hsp22, TRIM28, GJA1, TEX101, ARIH2, PLEKHA4, PINK1, YAP1, TFCP2, FANCD2, Clta, PXN, RALBP1, PTCHD3, C18orf54, ANKRD55, E, M, nsp13, nsp14, nsp4, nsp5, nsp6, ORF14, ORF3a, ORF6, ORF7a, ORF7b, ABCC2, CDCA5, ACO1, OPTN, NEK4, LRRC31, DUX4, CIT, AURKB, ECT2, KIF14, KIF20A, MAD2L2, KIF23, PRC1, PRNP, CHCHD1, HAX1, MFN2, SLC25A46, LDLR, SUMO2, PRKCB, Rnf183, AIMP2, BRD4, NINL, AFTPH, NUPR1, EPHA3, CIC, Apc2, RBM39, LGALS9, RIN3, EIF3H, DNAJA1, HSPA1L, HSPA2, HSPA6, BAG5, AR, UFL1, DDRGK1, CD3EAP, LAMTOR1, POLR2C, TRIM37, HTRA4, DRD2, ADRBK1, WDR5, PAGE4, NUDCD2, BGLT3, EDEM1, BAG2, DTX3, BTF3, IGF1R, NEDD4, FBXW7, TFRC, IFITM1, BSG, IFITM3, TMPRSS11B, CLEC4E, nsp15, ORF10, FGD5, MAP1LC3B, NBR1, CALCOCO2, SQSTM1, TOLLIP, Chrna4, SIRT6, PER2,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
MBTD1
CLTCall structure


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 MBTD1-CLTC


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 MBTD1-CLTC


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
TgeneCLTCC4518356MiT family translocation renal cell carcinoma2ORPHANET
TgeneCLTCC4693389MENTAL RETARDATION, AUTOSOMAL DOMINANT 562GENOMICS_ENGLAND;UNIPROT
TgeneCLTCC0079744Diffuse Large B-Cell Lymphoma1CTD_human
TgeneCLTCC0334121Inflammatory Myofibroblastic Tumor1ORPHANET