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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:CADM1-PARD6G

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CADM1-PARD6G
FusionPDB ID: 12445
FusionGDB2.0 ID: 12445
HgeneTgene
Gene symbol

CADM1

PARD6G

Gene ID

23705

84552

Gene namecell adhesion molecule 1par-6 family cell polarity regulator gamma
SynonymsBL2|IGSF4|IGSF4A|NECL2|Necl-2|RA175|ST17|SYNCAM|TSLC1|sTSLC-1|sgIGSF|synCAM1PAR-6G|PAR6gamma
Cytomap

11q23.3

18q23

Type of geneprotein-codingprotein-coding
Descriptioncell adhesion molecule 1TSLC-1TSLC1/Nectin-like 2/IGSF4immunoglobulin superfamily member 4immunoglobulin superfamily, member 4D variant 1immunoglobulin superfamily, member 4D variant 2nectin-like 2nectin-like protein 2spermatogenic immunoglobulin partitioning defective 6 homolog gammaPAR-6 gamma proteinPAR6Dpar-6 partitioning defective 6 homolog gamma
Modification date2020031320200327
UniProtAcc

Q9BY67

.
Ensembl transtripts involved in fusion geneENST idsENST00000537140, ENST00000331581, 
ENST00000452722, ENST00000536727, 
ENST00000537058, ENST00000542447, 
ENST00000353265, ENST00000470488, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score7 X 5 X 4=14010 X 3 X 8=240
# samples 810
** MAII scorelog2(8/140*10)=-0.807354922057604
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(10/240*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: CADM1 [Title/Abstract] AND PARD6G [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CADM1(115374988)-PARD6G(77960815), # samples:1
Anticipated loss of major functional domain due to fusion event.CADM1-PARD6G 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.
CADM1-PARD6G 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.
CADM1-PARD6G 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.
CADM1-PARD6G 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
HgeneCADM1

GO:0001913

T cell mediated cytotoxicity

15811952

HgeneCADM1

GO:0008037

cell recognition

15811952

HgeneCADM1

GO:0042271

susceptibility to natural killer cell mediated cytotoxicity

15811952

HgeneCADM1

GO:0045954

positive regulation of natural killer cell mediated cytotoxicity

15811952

HgeneCADM1

GO:0050715

positive regulation of cytokine secretion

15811952

HgeneCADM1

GO:0050798

activated T cell proliferation

15811952

HgeneCADM1

GO:0051606

detection of stimulus

15811952


check buttonFusion gene breakpoints across CADM1 (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 PARD6G (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
ChimerDB4OVTCGA-61-1910CADM1chr11

115374988

-PARD6Gchr18

77960815

-


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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)
ENST00000452722CADM1chr11115374988-ENST00000353265PARD6Gchr1877960815-37431451721203343
ENST00000452722CADM1chr11115374988-ENST00000470488PARD6Gchr1877960815-66914539364784
ENST00000542447CADM1chr11115374988-ENST00000353265PARD6Gchr1877960815-38512532801311343
ENST00000542447CADM1chr11115374988-ENST00000470488PARD6Gchr1877960815-7772532361119
ENST00000537058CADM1chr11115374988-ENST00000353265PARD6Gchr1877960815-37431451721203343
ENST00000537058CADM1chr11115374988-ENST00000470488PARD6Gchr1877960815-66914539364784
ENST00000536727CADM1chr11115374988-ENST00000353265PARD6Gchr1877960815-37431451721203343
ENST00000536727CADM1chr11115374988-ENST00000470488PARD6Gchr1877960815-66914539364784
ENST00000331581CADM1chr11115374988-ENST00000353265PARD6Gchr1877960815-38932953221353343
ENST00000331581CADM1chr11115374988-ENST00000470488PARD6Gchr1877960815-81929544403119

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
ENST00000452722ENST00000353265CADM1chr11115374988-PARD6Gchr1877960815-0.0046101590.9953898
ENST00000452722ENST00000470488CADM1chr11115374988-PARD6Gchr1877960815-0.169879110.83012086
ENST00000542447ENST00000353265CADM1chr11115374988-PARD6Gchr1877960815-0.0046985970.99530137
ENST00000542447ENST00000470488CADM1chr11115374988-PARD6Gchr1877960815-0.265648960.73435104
ENST00000537058ENST00000353265CADM1chr11115374988-PARD6Gchr1877960815-0.0046101590.9953898
ENST00000537058ENST00000470488CADM1chr11115374988-PARD6Gchr1877960815-0.169879110.83012086
ENST00000536727ENST00000353265CADM1chr11115374988-PARD6Gchr1877960815-0.0046101590.9953898
ENST00000536727ENST00000470488CADM1chr11115374988-PARD6Gchr1877960815-0.169879110.83012086
ENST00000331581ENST00000353265CADM1chr11115374988-PARD6Gchr1877960815-0.0047243990.9952756
ENST00000331581ENST00000470488CADM1chr11115374988-PARD6Gchr1877960815-0.269856630.7301433

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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

>12445_12445_1_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000331581_PARD6G_chr18_77960815_ENST00000353265_length(amino acids)=343AA_BP=
MDRHKPGKFEDFYKLVVHTHHISNSDVTIGYADVHGDLLPINNDDNFCKAVSSANPLLRVFIQKREEAERGSLGAGSLCRRRRALGALRD
EGPRRRAHLDIGLPRDFRPVSSIIDVDLVPETHRRVRLHRHGCEKPLGFYIRDGASVRVTPHGLEKVPGIFISRMVPGGLAESTGLLAVN
DEVLEVNGIEVAGKTLDQVTDMMIANSHNLIVTVKPANQRNNVVRGGRALGSSGPPSDGTAGFVGPPAPRVLQNFHPDEAESDEDNDVVI

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

>12445_12445_2_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000331581_PARD6G_chr18_77960815_ENST00000470488_length(amino acids)=119AA_BP=83
MGSRRCDWSARTPPPAHVISISLAVRSGSGGSQRRQSEAGARHGECSAAERIPVCGGSGGGGASRAPAPASAVALLRRGTDPHSLGRNSE

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

>12445_12445_3_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000452722_PARD6G_chr18_77960815_ENST00000353265_length(amino acids)=343AA_BP=
MDRHKPGKFEDFYKLVVHTHHISNSDVTIGYADVHGDLLPINNDDNFCKAVSSANPLLRVFIQKREEAERGSLGAGSLCRRRRALGALRD
EGPRRRAHLDIGLPRDFRPVSSIIDVDLVPETHRRVRLHRHGCEKPLGFYIRDGASVRVTPHGLEKVPGIFISRMVPGGLAESTGLLAVN
DEVLEVNGIEVAGKTLDQVTDMMIANSHNLIVTVKPANQRNNVVRGGRALGSSGPPSDGTAGFVGPPAPRVLQNFHPDEAESDEDNDVVI

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

>12445_12445_4_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000452722_PARD6G_chr18_77960815_ENST00000470488_length(amino acids)=84AA_BP=

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

>12445_12445_5_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000536727_PARD6G_chr18_77960815_ENST00000353265_length(amino acids)=343AA_BP=
MDRHKPGKFEDFYKLVVHTHHISNSDVTIGYADVHGDLLPINNDDNFCKAVSSANPLLRVFIQKREEAERGSLGAGSLCRRRRALGALRD
EGPRRRAHLDIGLPRDFRPVSSIIDVDLVPETHRRVRLHRHGCEKPLGFYIRDGASVRVTPHGLEKVPGIFISRMVPGGLAESTGLLAVN
DEVLEVNGIEVAGKTLDQVTDMMIANSHNLIVTVKPANQRNNVVRGGRALGSSGPPSDGTAGFVGPPAPRVLQNFHPDEAESDEDNDVVI

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

>12445_12445_6_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000536727_PARD6G_chr18_77960815_ENST00000470488_length(amino acids)=84AA_BP=

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

>12445_12445_7_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000537058_PARD6G_chr18_77960815_ENST00000353265_length(amino acids)=343AA_BP=
MDRHKPGKFEDFYKLVVHTHHISNSDVTIGYADVHGDLLPINNDDNFCKAVSSANPLLRVFIQKREEAERGSLGAGSLCRRRRALGALRD
EGPRRRAHLDIGLPRDFRPVSSIIDVDLVPETHRRVRLHRHGCEKPLGFYIRDGASVRVTPHGLEKVPGIFISRMVPGGLAESTGLLAVN
DEVLEVNGIEVAGKTLDQVTDMMIANSHNLIVTVKPANQRNNVVRGGRALGSSGPPSDGTAGFVGPPAPRVLQNFHPDEAESDEDNDVVI

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

>12445_12445_8_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000537058_PARD6G_chr18_77960815_ENST00000470488_length(amino acids)=84AA_BP=

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

>12445_12445_9_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000542447_PARD6G_chr18_77960815_ENST00000353265_length(amino acids)=343AA_BP=
MDRHKPGKFEDFYKLVVHTHHISNSDVTIGYADVHGDLLPINNDDNFCKAVSSANPLLRVFIQKREEAERGSLGAGSLCRRRRALGALRD
EGPRRRAHLDIGLPRDFRPVSSIIDVDLVPETHRRVRLHRHGCEKPLGFYIRDGASVRVTPHGLEKVPGIFISRMVPGGLAESTGLLAVN
DEVLEVNGIEVAGKTLDQVTDMMIANSHNLIVTVKPANQRNNVVRGGRALGSSGPPSDGTAGFVGPPAPRVLQNFHPDEAESDEDNDVVI

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

>12445_12445_10_CADM1-PARD6G_CADM1_chr11_115374988_ENST00000542447_PARD6G_chr18_77960815_ENST00000470488_length(amino acids)=119AA_BP=83
LGSRRCDWSARTPPPAHVISISLAVRSGSGGSQRRQSEAGARHGECSAAERIPVCGGSGGGGASRAPAPASAVALLRRGTDPHSLGRNSE

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

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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/chr11:115374988/chr18:77960815)
- 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
CADM1

Q9BY67

.
FUNCTION: Mediates homophilic cell-cell adhesion in a Ca(2+)-independent manner (PubMed:22438059, PubMed:12050160). Also mediates heterophilic cell-cell adhesion with CADM3 and NECTIN3 in a Ca(2+)-independent manner (By similarity). Interaction with CRTAM promotes natural killer (NK) cell cytotoxicity and interferon-gamma (IFN-gamma) secretion by CD8+ cells in vitro as well as NK cell-mediated rejection of tumors expressing CADM1 in vivo (PubMed:15811952). In mast cells, may mediate attachment to and promote communication with nerves (PubMed:15905536). CADM1, together with MITF, is essential for development and survival of mast cells in vivo (PubMed:22438059). By interacting with CRTAM and thus promoting the adhesion between CD8+ T-cells and CD8+ dendritic cells, regulates the retention of activated CD8+ T-cell within the draining lymph node (By similarity). Required for the intestinal retention of intraepithelial CD4+ CD8+ T-cells and, to a lesser extent, intraepithelial and lamina propria CD8+ T-cells and CD4+ T-cells (By similarity). Interaction with CRTAM promotes the adhesion to gut-associated CD103+ dendritic cells, which may facilitate the expression of gut-homing and adhesion molecules on T-cells and the conversion of CD4+ T-cells into CD4+ CD8+ T-cells (By similarity). Acts as a synaptic cell adhesion molecule and plays a role in the formation of dendritic spines and in synapse assembly (By similarity). May be involved in neuronal migration, axon growth, pathfinding, and fasciculation on the axons of differentiating neurons (By similarity). May play diverse roles in the spermatogenesis including in the adhesion of spermatocytes and spermatids to Sertoli cells and for their normal differentiation into mature spermatozoa (By similarity). Acts as a tumor suppressor in non-small-cell lung cancer (NSCLC) cells (PubMed:11279526, PubMed:12234973). May contribute to the less invasive phenotypes of lepidic growth tumor cells (PubMed:12920246). {ECO:0000250|UniProtKB:Q8R5M8, ECO:0000269|PubMed:11279526, ECO:0000269|PubMed:12050160, ECO:0000269|PubMed:12234973, ECO:0000269|PubMed:12920246, ECO:0000269|PubMed:15811952, ECO:0000269|PubMed:15905536, ECO:0000269|PubMed:22438059}.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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgenePARD6Gchr11:115374988chr18:77960815ENST0000035326503134_15124.0377.0DomainNote=Pseudo-CRIB
TgenePARD6Gchr11:115374988chr18:77960815ENST0000035326503158_25124.0377.0DomainPDZ
TgenePARD6Gchr11:115374988chr18:77960815ENST0000047048803134_15124.0108.0DomainNote=Pseudo-CRIB
TgenePARD6Gchr11:115374988chr18:77960815ENST0000047048803158_25124.0108.0DomainPDZ

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCADM1chr11:115374988chr18:77960815ENST00000331581-112144_23841.333333333333336472.0DomainIg-like C2-type 1
HgeneCADM1chr11:115374988chr18:77960815ENST00000331581-112243_32941.333333333333336472.0DomainIg-like C2-type 2
HgeneCADM1chr11:115374988chr18:77960815ENST00000331581-11245_13941.333333333333336472.0DomainIg-like V-type
HgeneCADM1chr11:115374988chr18:77960815ENST00000452722-110144_23841.333333333333336443.0DomainIg-like C2-type 1
HgeneCADM1chr11:115374988chr18:77960815ENST00000452722-110243_32941.333333333333336443.0DomainIg-like C2-type 2
HgeneCADM1chr11:115374988chr18:77960815ENST00000452722-11045_13941.333333333333336443.0DomainIg-like V-type
HgeneCADM1chr11:115374988chr18:77960815ENST00000537058-111144_23841.333333333333336454.0DomainIg-like C2-type 1
HgeneCADM1chr11:115374988chr18:77960815ENST00000537058-111243_32941.333333333333336454.0DomainIg-like C2-type 2
HgeneCADM1chr11:115374988chr18:77960815ENST00000537058-11145_13941.333333333333336454.0DomainIg-like V-type
HgeneCADM1chr11:115374988chr18:77960815ENST00000542447-19144_23841.333333333333336415.0DomainIg-like C2-type 1
HgeneCADM1chr11:115374988chr18:77960815ENST00000542447-19243_32941.333333333333336415.0DomainIg-like C2-type 2
HgeneCADM1chr11:115374988chr18:77960815ENST00000542447-1945_13941.333333333333336415.0DomainIg-like V-type
HgeneCADM1chr11:115374988chr18:77960815ENST00000331581-112396_44241.333333333333336472.0Topological domainCytoplasmic
HgeneCADM1chr11:115374988chr18:77960815ENST00000331581-11245_37441.333333333333336472.0Topological domainExtracellular
HgeneCADM1chr11:115374988chr18:77960815ENST00000452722-110396_44241.333333333333336443.0Topological domainCytoplasmic
HgeneCADM1chr11:115374988chr18:77960815ENST00000452722-11045_37441.333333333333336443.0Topological domainExtracellular
HgeneCADM1chr11:115374988chr18:77960815ENST00000537058-111396_44241.333333333333336454.0Topological domainCytoplasmic
HgeneCADM1chr11:115374988chr18:77960815ENST00000537058-11145_37441.333333333333336454.0Topological domainExtracellular
HgeneCADM1chr11:115374988chr18:77960815ENST00000542447-19396_44241.333333333333336415.0Topological domainCytoplasmic
HgeneCADM1chr11:115374988chr18:77960815ENST00000542447-1945_37441.333333333333336415.0Topological domainExtracellular
HgeneCADM1chr11:115374988chr18:77960815ENST00000331581-112375_39541.333333333333336472.0TransmembraneHelical
HgeneCADM1chr11:115374988chr18:77960815ENST00000452722-110375_39541.333333333333336443.0TransmembraneHelical
HgeneCADM1chr11:115374988chr18:77960815ENST00000537058-111375_39541.333333333333336454.0TransmembraneHelical
HgeneCADM1chr11:115374988chr18:77960815ENST00000542447-19375_39541.333333333333336415.0TransmembraneHelical
TgenePARD6Gchr11:115374988chr18:77960815ENST000003532650318_9824.0377.0DomainPB1
TgenePARD6Gchr11:115374988chr18:77960815ENST000004704880318_9824.0108.0DomainPB1


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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


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
CADM1
PARD6G


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 CADM1-PARD6G


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 CADM1-PARD6G


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