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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:CRIM1-TACR1 (FusionGDB2 ID:19450)

Fusion Gene Summary for CRIM1-TACR1

check button Fusion gene summary
Fusion gene informationFusion gene name: CRIM1-TACR1
Fusion gene ID: 19450
HgeneTgene
Gene symbol

CRIM1

TACR1

Gene ID

51232

6869

Gene namecysteine rich transmembrane BMP regulator 1tachykinin receptor 1
SynonymsCRIM-1|S52NK1R|NKIR|SPR|TAC1R
Cytomap

2p22.2

2p12

Type of geneprotein-codingprotein-coding
Descriptioncysteine-rich motor neuron 1 proteincysteine rich transmembrane BMP regulator 1 (chordin-like)cysteine-rich repeat-containing protein S52substance-P receptorNK-1 receptorNK-1Rtachykinin receptor 1 (substance P receptor; neurokinin-1 receptor)
Modification date2020031320200313
UniProtAcc

Q9NZV1

.
Ensembl transtripts involved in fusion geneENST00000280527, ENST00000473403, 
ENST00000305249, ENST00000409848, 
ENST00000497764, 
Fusion gene scores* DoF score15 X 11 X 8=13203 X 3 X 3=27
# samples 163
** MAII scorelog2(16/1320*10)=-3.04439411935845
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: CRIM1 [Title/Abstract] AND TACR1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCRIM1(36749456)-TACR1(75347894), # samples:3
Anticipated loss of major functional domain due to fusion event.CRIM1-TACR1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
CRIM1-TACR1 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target 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
TgeneTACR1

GO:0007204

positive regulation of cytosolic calcium ion concentration

12716968

TgeneTACR1

GO:0007217

tachykinin receptor signaling pathway

17986524


check buttonFusion gene breakpoints across CRIM1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across TACR1 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4KIRCTCGA-CJ-5681-01ACRIM1chr2

36749456

+TACR1chr2

75347894

-
ChimerDB4KIRCTCGA-CJ-5681-01ACRIM1chr2

36749456

+TACR1chr2

75347894

-
ChimerDB4KIRCTCGA-CJ-5681-01ACRIM1chr2

36764689

+TACR1chr2

75347894

-
ChimerDB4KIRCTCGA-CJ-5681-01ACRIM1chr2

36749456

-TACR1chr2

75347894

-


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Fusion Gene ORF analysis for CRIM1-TACR1

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
Frame-shiftENST00000280527ENST00000305249CRIM1chr2

36749456

+TACR1chr2

75347894

-
Frame-shiftENST00000280527ENST00000409848CRIM1chr2

36749456

+TACR1chr2

75347894

-
Frame-shiftENST00000280527ENST00000497764CRIM1chr2

36749456

+TACR1chr2

75347894

-
intron-3CDSENST00000473403ENST00000305249CRIM1chr2

36749456

+TACR1chr2

75347894

-
intron-3CDSENST00000473403ENST00000409848CRIM1chr2

36749456

+TACR1chr2

75347894

-
intron-3CDSENST00000473403ENST00000497764CRIM1chr2

36749456

+TACR1chr2

75347894

-
Frame-shiftENST00000280527ENST00000305249CRIM1chr2

36764689

+TACR1chr2

75347894

-
Frame-shiftENST00000280527ENST00000409848CRIM1chr2

36764689

+TACR1chr2

75347894

-
Frame-shiftENST00000280527ENST00000497764CRIM1chr2

36764689

+TACR1chr2

75347894

-
intron-3CDSENST00000473403ENST00000305249CRIM1chr2

36764689

+TACR1chr2

75347894

-
intron-3CDSENST00000473403ENST00000409848CRIM1chr2

36764689

+TACR1chr2

75347894

-
intron-3CDSENST00000473403ENST00000497764CRIM1chr2

36764689

+TACR1chr2

75347894

-

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)

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

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Fusion Genomic Features for CRIM1-TACR1


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)

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.

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.

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Fusion Protein Features for CRIM1-TACR1


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CRIM1

Q9NZV1

.
FUNCTION: May play a role in CNS development by interacting with growth factors implicated in motor neuron differentiation and survival. May play a role in capillary formation and maintenance during angiogenesis. Modulates BMP activity by affecting its processing and delivery to the cell surface. {ECO:0000269|PubMed:12464430, ECO:0000269|PubMed:12805376}.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.
- In-frame and retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for CRIM1-TACR1


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.

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Fusion Gene PPI Analysis for CRIM1-TACR1


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 CRIM1-TACR1


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 CRIM1-TACR1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCRIM1C1865286MACROPHTHALMIA, COLOBOMATOUS, WITH MICROCORNEA2GENOMICS_ENGLAND;ORPHANET
TgeneTACR1C0001973Alcoholic Intoxication, Chronic5CTD_human;PSYGENET
TgeneTACR1C0011570Mental Depression5PSYGENET
TgeneTACR1C0011581Depressive disorder5PSYGENET
TgeneTACR1C0525045Mood Disorders5PSYGENET
TgeneTACR1C0005586Bipolar Disorder3CTD_human;PSYGENET
TgeneTACR1C0020429Hyperalgesia2CTD_human
TgeneTACR1C0458247Allodynia2CTD_human
TgeneTACR1C0600467Neurogenic Inflammation2CTD_human
TgeneTACR1C0751211Hyperalgesia, Primary2CTD_human
TgeneTACR1C0751212Hyperalgesia, Secondary2CTD_human
TgeneTACR1C0751213Tactile Allodynia2CTD_human
TgeneTACR1C0751214Hyperalgesia, Thermal2CTD_human
TgeneTACR1C2936719Mechanical Allodynia2CTD_human
TgeneTACR1C0001956Alcohol Use Disorder1CTD_human
TgeneTACR1C0005587Depression, Bipolar1CTD_human
TgeneTACR1C0006261Bronchial Diseases1CTD_human
TgeneTACR1C0020538Hypertensive disease1CTD_human
TgeneTACR1C0024713Manic Disorder1CTD_human
TgeneTACR1C0038587Substance Withdrawal Syndrome1CTD_human
TgeneTACR1C0041671Attention Deficit Disorder1CTD_human
TgeneTACR1C0042963Vomiting1CTD_human
TgeneTACR1C0085762Alcohol abuse1CTD_human
TgeneTACR1C0086189Drug Withdrawal Symptoms1CTD_human
TgeneTACR1C0087169Withdrawal Symptoms1CTD_human
TgeneTACR1C0338831Manic1CTD_human
TgeneTACR1C0428977Bradycardia1CTD_human
TgeneTACR1C1263846Attention deficit hyperactivity disorder1CTD_human
TgeneTACR1C1321905Minimal Brain Dysfunction1CTD_human