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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:CRELD1-FANCD2

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: CRELD1-FANCD2
FusionPDB ID: 19413
FusionGDB2.0 ID: 19413
HgeneTgene
Gene symbol

CRELD1

FANCD2

Gene ID

78987

2177

Gene namecysteine rich with EGF like domains 1FA complementation group D2
SynonymsAVSD2|CIRRINFA-D2|FA4|FACD|FAD|FAD2|FANCD
Cytomap

3p25.3

3p25.3

Type of geneprotein-codingprotein-coding
Descriptionprotein disulfide isomerase CRELD1Fanconi anemia group D2 proteinFanconi anemia complementation group D2
Modification date2020031320200313
UniProtAcc

Q96HD1

Q96PS1

Ensembl transtripts involved in fusion geneENST idsENST00000489674, ENST00000326434, 
ENST00000383811, ENST00000397170, 
ENST00000452070, 
ENST00000287647, 
ENST00000383806, ENST00000383807, 
ENST00000419585, ENST00000431693, 
ENST00000438741, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 4 X 3=369 X 13 X 7=819
# samples 411
** MAII scorelog2(4/36*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(11/819*10)=-2.89635992811635
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: CRELD1 [Title/Abstract] AND FANCD2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)CRELD1(9985199)-FANCD2(10133865), # samples:1
Anticipated loss of major functional domain due to fusion event.CRELD1-FANCD2 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.
CRELD1-FANCD2 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.
CRELD1-FANCD2 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.
CRELD1-FANCD2 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.
CRELD1-FANCD2 seems lost the major protein functional domain in Tgene partner, which is a CGC 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
TgeneFANCD2

GO:0010332

response to gamma radiation

12874027


check buttonFusion gene breakpoints across CRELD1 (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 FANCD2 (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
ChimerDB4LGGTCGA-S9-A6WM-01ACRELD1chr3

9985199

+FANCD2chr3

10133865

+


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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)
ENST00000397170CRELD1chr39985199+ENST00000383806FANCD2chr310133865+23451098501105351
ENST00000383811CRELD1chr39985199+ENST00000383806FANCD2chr310133865+289416475991654351
ENST00000452070CRELD1chr39985199+ENST00000383806FANCD2chr310133865+23901143951150351
ENST00000326434CRELD1chr39985199+ENST00000383806FANCD2chr310133865+23791132841139351

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
ENST00000397170ENST00000383806CRELD1chr39985199+FANCD2chr310133865+0.0049578730.9950421
ENST00000383811ENST00000383806CRELD1chr39985199+FANCD2chr310133865+0.0050082170.99499184
ENST00000452070ENST00000383806CRELD1chr39985199+FANCD2chr310133865+0.0043540910.99564594
ENST00000326434ENST00000383806CRELD1chr39985199+FANCD2chr310133865+0.0043102370.9956898

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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

>19413_19413_1_CRELD1-FANCD2_CRELD1_chr3_9985199_ENST00000326434_FANCD2_chr3_10133865_ENST00000383806_length(amino acids)=351AA_BP=
MAPWPPKGLVPAMLWGLSLFLNLPGPIWLQPSPPPQSSPPPQPHPCHTCRGLVDSFNKGLERTIRDNFGGGNTAWEEENLSKYKDSETRL
VEVLEGVCSKSDFECHRLLELSEELVESWWFHKQQEAPDLFQWLCSDSLKLCCPAGTFGPSCLPCPGGTERPCGGYGQCEGEGTRGGSGH
CDCQAGYGGEACGQCGLGYFEAERNASHLVCSACFGPCARCSGPEESNCLQCKKGWALHHLKCVDIDECGTEGANCGADQFCVNTEGSYE

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

>19413_19413_2_CRELD1-FANCD2_CRELD1_chr3_9985199_ENST00000383811_FANCD2_chr3_10133865_ENST00000383806_length(amino acids)=351AA_BP=
MAPWPPKGLVPAMLWGLSLFLNLPGPIWLQPSPPPQSSPPPQPHPCHTCRGLVDSFNKGLERTIRDNFGGGNTAWEEENLSKYKDSETRL
VEVLEGVCSKSDFECHRLLELSEELVESWWFHKQQEAPDLFQWLCSDSLKLCCPAGTFGPSCLPCPGGTERPCGGYGQCEGEGTRGGSGH
CDCQAGYGGEACGQCGLGYFEAERNASHLVCSACFGPCARCSGPEESNCLQCKKGWALHHLKCVDIDECGTEGANCGADQFCVNTEGSYE

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

>19413_19413_3_CRELD1-FANCD2_CRELD1_chr3_9985199_ENST00000397170_FANCD2_chr3_10133865_ENST00000383806_length(amino acids)=351AA_BP=
MAPWPPKGLVPAMLWGLSLFLNLPGPIWLQPSPPPQSSPPPQPHPCHTCRGLVDSFNKGLERTIRDNFGGGNTAWEEENLSKYKDSETRL
VEVLEGVCSKSDFECHRLLELSEELVESWWFHKQQEAPDLFQWLCSDSLKLCCPAGTFGPSCLPCPGGTERPCGGYGQCEGEGTRGGSGH
CDCQAGYGGEACGQCGLGYFEAERNASHLVCSACFGPCARCSGPEESNCLQCKKGWALHHLKCVDIDECGTEGANCGADQFCVNTEGSYE

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

>19413_19413_4_CRELD1-FANCD2_CRELD1_chr3_9985199_ENST00000452070_FANCD2_chr3_10133865_ENST00000383806_length(amino acids)=351AA_BP=
MAPWPPKGLVPAMLWGLSLFLNLPGPIWLQPSPPPQSSPPPQPHPCHTCRGLVDSFNKGLERTIRDNFGGGNTAWEEENLSKYKDSETRL
VEVLEGVCSKSDFECHRLLELSEELVESWWFHKQQEAPDLFQWLCSDSLKLCCPAGTFGPSCLPCPGGTERPCGGYGQCEGEGTRGGSGH
CDCQAGYGGEACGQCGLGYFEAERNASHLVCSACFGPCARCSGPEESNCLQCKKGWALHHLKCVDIDECGTEGANCGADQFCVNTEGSYE

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

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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/chr3:9985199/chr3:10133865)
- 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
CRELD1

Q96HD1

FANCD2

Q96PS1

FUNCTION: Protein disulfide isomerase (By similarity). Promotes the localization of acetylcholine receptors (AChRs) to the plasma membrane (By similarity). {ECO:0000250|UniProtKB:Q91XD7, ECO:0000250|UniProtKB:Q9CYA0}.

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
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+10123_45349.3333333333333423.0Compositional biasNote=Pro-rich
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+9103_45349.3333333333333421.0Compositional biasNote=Pro-rich
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+10113_45349.3333333333333421.0Compositional biasNote=Pro-rich
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+10113_45349.3333333333333421.0Compositional biasNote=Pro-rich
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+1012153_193349.3333333333333423.0DomainEGF-like 1
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+1012305_344349.3333333333333423.0DomainEGF-like 2%3B calcium-binding
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+910153_193349.3333333333333421.0DomainEGF-like 1
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+910305_344349.3333333333333421.0DomainEGF-like 2%3B calcium-binding
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+1011153_193349.3333333333333421.0DomainEGF-like 1
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+1011305_344349.3333333333333421.0DomainEGF-like 2%3B calcium-binding
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+1011153_193349.3333333333333421.0DomainEGF-like 1
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+1011305_344349.3333333333333421.0DomainEGF-like 2%3B calcium-binding
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+1012208_256349.3333333333333423.0RepeatNote=FU 1
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+1012268_315349.3333333333333423.0RepeatNote=FU 2
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+910208_256349.3333333333333421.0RepeatNote=FU 1
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+910268_315349.3333333333333421.0RepeatNote=FU 2
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+1011208_256349.3333333333333421.0RepeatNote=FU 1
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+1011268_315349.3333333333333421.0RepeatNote=FU 2
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+1011208_256349.3333333333333421.0RepeatNote=FU 1
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+1011268_315349.3333333333333421.0RepeatNote=FU 2

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+101230_362349.3333333333333423.0Topological domainExtracellular
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+1012384_384349.3333333333333423.0Topological domainCytoplasmic
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+1012406_420349.3333333333333423.0Topological domainExtracellular
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+91030_362349.3333333333333421.0Topological domainExtracellular
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+910384_384349.3333333333333421.0Topological domainCytoplasmic
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+910406_420349.3333333333333421.0Topological domainExtracellular
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+101130_362349.3333333333333421.0Topological domainExtracellular
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+1011384_384349.3333333333333421.0Topological domainCytoplasmic
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+1011406_420349.3333333333333421.0Topological domainExtracellular
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+101130_362349.3333333333333421.0Topological domainExtracellular
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+1011384_384349.3333333333333421.0Topological domainCytoplasmic
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+1011406_420349.3333333333333421.0Topological domainExtracellular
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+1012363_383349.3333333333333423.0TransmembraneHelical
HgeneCRELD1chr3:9985199chr3:10133865ENST00000326434+1012385_405349.3333333333333423.0TransmembraneHelical
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+910363_383349.3333333333333421.0TransmembraneHelical
HgeneCRELD1chr3:9985199chr3:10133865ENST00000383811+910385_405349.3333333333333421.0TransmembraneHelical
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+1011363_383349.3333333333333421.0TransmembraneHelical
HgeneCRELD1chr3:9985199chr3:10133865ENST00000397170+1011385_405349.3333333333333421.0TransmembraneHelical
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+1011363_383349.3333333333333421.0TransmembraneHelical
HgeneCRELD1chr3:9985199chr3:10133865ENST00000452070+1011385_405349.3333333333333421.0TransmembraneHelical


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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
CRELD1
FANCD2


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
TgeneFANCD2chr3:9985199chr3:10133865ENST000002876473643248_3591259.01472.0BRCA2
TgeneFANCD2chr3:9985199chr3:10133865ENST000003838063543248_3591227.66666666666671469.6666666666667BRCA2
TgeneFANCD2chr3:9985199chr3:10133865ENST000003838073644248_3591259.01452.0BRCA2
TgeneFANCD2chr3:9985199chr3:10133865ENST000004195853644248_3591259.01452.0BRCA2
TgeneFANCD2chr3:9985199chr3:10133865ENST0000028764736431_2911259.01472.0FANCE
TgeneFANCD2chr3:9985199chr3:10133865ENST0000038380635431_2911227.66666666666671469.6666666666667FANCE
TgeneFANCD2chr3:9985199chr3:10133865ENST0000038380736441_2911259.01452.0FANCE
TgeneFANCD2chr3:9985199chr3:10133865ENST0000041958536441_2911259.01452.0FANCE


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Related Drugs to CRELD1-FANCD2


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 CRELD1-FANCD2


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