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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:CCDC144NL-AMACR (FusionGDB2 ID:HG339184TG23600)

Fusion Gene Summary for CCDC144NL-AMACR

check button Fusion gene summary
Fusion gene informationFusion gene name: CCDC144NL-AMACR
Fusion gene ID: hg339184tg23600
HgeneTgene
Gene symbol

CCDC144NL

AMACR

Gene ID

339184

23600

Gene namealpha-methylacyl-CoA racemase
SynonymsAMACRD|CBAS4|P504S|RACE|RM
Cytomap('CCDC144NL')('AMACR')

5p13.2

Type of geneprotein-coding
Descriptionalpha-methylacyl-CoA racemase2-methylacyl-CoA racemase
Modification date20200313
UniProtAcc

Q6NUI1

Q9UHK6

Ensembl transtripts involved in fusion geneENST00000327925, ENST00000539484, 
Fusion gene scores* DoF score4 X 5 X 3=6028 X 3 X 4=336
# samples 423
** MAII scorelog2(4/60*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(23/336*10)=-0.546827371834385
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CCDC144NL [Title/Abstract] AND AMACR [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointCCDC144NL(20796705)-AMACR(34006004), # samples:1
CCDC144NL(20768732)-AMACR(34006004), # samples:1
Anticipated loss of major functional domain due to fusion event.CCDC144NL-AMACR 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.
CCDC144NL-AMACR 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.
CCDC144NL-AMACR 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.
CCDC144NL-AMACR 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
TgeneAMACR

GO:0008206

bile acid metabolic process

10655068


check buttonFusion gene breakpoints across CCDC144NL (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 AMACR (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check button Fusion gene information
* 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
ChimerDB4PRADTCGA-YL-A8SCCCDC144NLchr17

20768732

-AMACRchr5

34006004

-
ChimerDB4PRADTCGA-YL-A8SCCCDC144NLchr17

20796705

-AMACRchr5

34006004

-


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Fusion Gene ORF analysis for CCDC144NL-AMACR

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
5CDS-5UTRENST00000327925ENST00000382068CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
5CDS-5UTRENST00000327925ENST00000382085CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
5CDS-5UTRENST00000327925ENST00000426255CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
5CDS-5UTRENST00000327925ENST00000441713CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
5CDS-5UTRENST00000327925ENST00000502637CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
5CDS-5UTRENST00000327925ENST00000512079CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
5CDS-5UTRENST00000327925ENST00000514195CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
5UTR-3CDSENST00000539484ENST00000335606CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
5UTR-3CDSENST00000539484ENST00000382072CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
5UTR-5UTRENST00000539484ENST00000382068CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
5UTR-5UTRENST00000539484ENST00000382085CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
5UTR-5UTRENST00000539484ENST00000426255CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
5UTR-5UTRENST00000539484ENST00000441713CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
5UTR-5UTRENST00000539484ENST00000502637CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
5UTR-5UTRENST00000539484ENST00000512079CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
5UTR-5UTRENST00000539484ENST00000514195CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
In-frameENST00000327925ENST00000335606CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
In-frameENST00000327925ENST00000382072CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
intron-3CDSENST00000327925ENST00000335606CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
intron-3CDSENST00000327925ENST00000382072CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
intron-3CDSENST00000539484ENST00000335606CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
intron-3CDSENST00000539484ENST00000382072CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
intron-5UTRENST00000327925ENST00000382068CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
intron-5UTRENST00000327925ENST00000382085CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
intron-5UTRENST00000327925ENST00000426255CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
intron-5UTRENST00000327925ENST00000441713CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
intron-5UTRENST00000327925ENST00000502637CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
intron-5UTRENST00000327925ENST00000512079CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
intron-5UTRENST00000327925ENST00000514195CCDC144NLchr17

20768732

-AMACRchr5

34006004

-
intron-5UTRENST00000539484ENST00000382068CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
intron-5UTRENST00000539484ENST00000382085CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
intron-5UTRENST00000539484ENST00000426255CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
intron-5UTRENST00000539484ENST00000441713CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
intron-5UTRENST00000539484ENST00000502637CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
intron-5UTRENST00000539484ENST00000512079CCDC144NLchr17

20796705

-AMACRchr5

34006004

-
intron-5UTRENST00000539484ENST00000514195CCDC144NLchr17

20796705

-AMACRchr5

34006004

-

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)
ENST00000327925CCDC144NLchr1720796705-ENST00000335606AMACRchr534006004-4352535211436471
ENST00000327925CCDC144NLchr1720796705-ENST00000382072AMACRchr534006004-319553521884287

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
ENST00000327925ENST00000335606CCDC144NLchr1720796705-AMACRchr534006004-0.0002351470.99976486
ENST00000327925ENST00000382072CCDC144NLchr1720796705-AMACRchr534006004-0.0053626990.9946373

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Fusion Genomic Features for CCDC144NL-AMACR


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.
genomic feature

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Fusion Protein Features for CCDC144NL-AMACR


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/chr17:20796705/chr5:34006004)
- 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
CCDC144NL

Q6NUI1

AMACR

Q9UHK6

FUNCTION: Catalyzes the interconversion of (R)- and (S)-stereoisomers of alpha-methyl-branched-chain fatty acyl-CoA esters (PubMed:7649182, PubMed:10655068, PubMed:11060359). Acts only on coenzyme A thioesters, not on free fatty acids, and accepts as substrates a wide range of alpha-methylacyl-CoAs, including pristanoyl-CoA, trihydroxycoprostanoyl-CoA (an intermediate in bile acid synthesis), and arylpropionic acids like the anti-inflammatory drug ibuprofen (2-(4-isobutylphenyl)propionic acid) but neither 3-methyl-branched nor linear-chain acyl-CoAs (PubMed:7649182, PubMed:10655068, PubMed:11060359). {ECO:0000269|PubMed:10655068, ECO:0000269|PubMed:11060359, ECO:0000269|PubMed:7649182}.

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
TgeneAMACRchr17:20796705chr5:34006004ENST0000033560605380_38282383.0MotifMicrobody targeting signal
TgeneAMACRchr17:20796705chr5:34006004ENST0000038207204380_38282199.0MotifMicrobody targeting signal
TgeneAMACRchr17:20796705chr5:34006004ENST0000038208506380_38282395.0MotifMicrobody targeting signal
TgeneAMACRchr17:20796705chr5:34006004ENST0000044171304380_38282230.0MotifMicrobody targeting signal
TgeneAMACRchr17:20796705chr5:34006004ENST0000033560605121_12682383.0RegionSubstrate binding
TgeneAMACRchr17:20796705chr5:34006004ENST0000038207204121_12682199.0RegionSubstrate binding
TgeneAMACRchr17:20796705chr5:34006004ENST0000038208506121_12682395.0RegionSubstrate binding
TgeneAMACRchr17:20796705chr5:34006004ENST0000044171304121_12682230.0RegionSubstrate binding

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
TgeneAMACRchr17:20796705chr5:34006004ENST000003356060555_5882383.0RegionSubstrate binding
TgeneAMACRchr17:20796705chr5:34006004ENST000003820720455_5882199.0RegionSubstrate binding
TgeneAMACRchr17:20796705chr5:34006004ENST000003820850655_5882395.0RegionSubstrate binding
TgeneAMACRchr17:20796705chr5:34006004ENST000004417130455_5882230.0RegionSubstrate binding


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Fusion Gene Sequence for CCDC144NL-AMACR


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 CCDC144NL-AMACR


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 CCDC144NL-AMACR


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 CCDC144NL-AMACR


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC0033578Prostatic Neoplasms3CTD_human
TgeneC0376358Malignant neoplasm of prostate3CTD_human
TgeneC1858328Bile acid synthesis defect, congenital, 43CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneC3280428Alpha-Methylacyl-CoA Racemase Deficiency3CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT
TgeneC0023893Liver Cirrhosis, Experimental2CTD_human
TgeneC0001430Adenoma1CTD_human
TgeneC0009402Colorectal Carcinoma1CTD_human
TgeneC0009404Colorectal Neoplasms1CTD_human
TgeneC0011195Dejerine-Sottas Disease (disorder)1CTD_human
TgeneC0019816Hereditary, Type VII, Motor and Sensory Neuropathy1CTD_human
TgeneC0023895Liver diseases1CTD_human
TgeneC0027888Hereditary Motor and Sensory Neuropathies1CTD_human
TgeneC0036341Schizophrenia1PSYGENET
TgeneC0086565Liver Dysfunction1CTD_human
TgeneC0205646Adenoma, Basal Cell1CTD_human
TgeneC0205647Follicular adenoma1CTD_human
TgeneC0205648Adenoma, Microcystic1CTD_human
TgeneC0205649Adenoma, Monomorphic1CTD_human
TgeneC0205650Papillary adenoma1CTD_human
TgeneC0205651Adenoma, Trabecular1CTD_human