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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:MLYCD-NKAIN4

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: MLYCD-NKAIN4
FusionPDB ID: 54365
FusionGDB2.0 ID: 54365
HgeneTgene
Gene symbol

MLYCD

NKAIN4

Gene ID

23417

128414

Gene namemalonyl-CoA decarboxylasesodium/potassium transporting ATPase interacting 4
SynonymsMCDC20orf58|FAM77A|bA261N11.2
Cytomap

16q23.3

20q13.33

Type of geneprotein-codingprotein-coding
Descriptionmalonyl-CoA decarboxylase, mitochondrialmalonyl coenzyme A decarboxylasesodium/potassium-transporting ATPase subunit beta-1-interacting protein 4Na(+)/K(+)-transporting ATPase subunit beta-1-interacting protein 4Na+/K+ transporting ATPase interacting 4
Modification date2020031320200313
UniProtAcc

O95822

Q8IVV8

Ensembl transtripts involved in fusion geneENST idsENST00000262430, ENST00000370307, 
ENST00000466885, ENST00000370313, 
ENST00000370316, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score3 X 3 X 3=275 X 5 X 3=75
# samples 35
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/75*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: MLYCD [Title/Abstract] AND NKAIN4 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)MLYCD(83933151)-NKAIN4(61880247), # samples:1
Anticipated loss of major functional domain due to fusion event.MLYCD-NKAIN4 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.
MLYCD-NKAIN4 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
HgeneMLYCD

GO:0006085

acetyl-CoA biosynthetic process

9869665|10417274|10455107

HgeneMLYCD

GO:0006633

fatty acid biosynthetic process

15003260

HgeneMLYCD

GO:2001294

malonyl-CoA catabolic process

10417274|10455107|15003260


check buttonFusion gene breakpoints across MLYCD (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 NKAIN4 (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-TQ-A7ROMLYCDchr16

83933151

+NKAIN4chr20

61880247

-


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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)
ENST00000262430MLYCDchr1683933151+ENST00000370313NKAIN4chr2061880247-11891265551016153
ENST00000262430MLYCDchr1683933151+ENST00000370316NKAIN4chr2061880247-127412636560174

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
ENST00000262430ENST00000370313MLYCDchr1683933151+NKAIN4chr2061880247-0.8827470.117253006
ENST00000262430ENST00000370316MLYCDchr1683933151+NKAIN4chr2061880247-0.861313760.13868618

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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

>54365_54365_1_MLYCD-NKAIN4_MLYCD_chr16_83933151_ENST00000262430_NKAIN4_chr20_61880247_ENST00000370313_length(amino acids)=153AA_BP=
MGRAPTQHPPGGRQHLPWVLSTGHQPGRQGSATAGCSVKRVCNFLSLKKKKEKKTYKRKGKTPHAHLLWQHGGHSSAPRLSSRRGAPPSG

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

>54365_54365_2_MLYCD-NKAIN4_MLYCD_chr16_83933151_ENST00000262430_NKAIN4_chr20_61880247_ENST00000370316_length(amino acids)=174AA_BP=30
MDGGVRFLVQLRADLLEAQALKLVEGPDVRYTLWAAVWVTWNVFIICFYLEVGGLLKDSELLTFSLSRHRSWWRERWPGCLHEEVPAVGL

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

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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/chr16:83933151/chr20:61880247)
- 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
MLYCD

O95822

NKAIN4

Q8IVV8

FUNCTION: Catalyzes the conversion of malonyl-CoA to acetyl-CoA. In the fatty acid biosynthesis MCD selectively removes malonyl-CoA and thus assures that methyl-malonyl-CoA is the only chain elongating substrate for fatty acid synthase and that fatty acids with multiple methyl side chains are produced. In peroxisomes it may be involved in degrading intraperoxisomal malonyl-CoA, which is generated by the peroxisomal beta-oxidation of odd chain-length dicarboxylic fatty acids. Plays a role in the metabolic balance between glucose and lipid oxidation in muscle independent of alterations in insulin signaling. May play a role in controlling the extent of ischemic injury by promoting glucose oxidation. {ECO:0000269|PubMed:10455107, ECO:0000269|PubMed:15003260, ECO:0000269|PubMed:18314420, ECO:0000269|PubMed:23482565}.

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
TgeneNKAIN4chr16:83933151chr20:61880247ENST0000037031617151_17164.0209.0TransmembraneHelical
TgeneNKAIN4chr16:83933151chr20:61880247ENST000003703161762_8264.0209.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMLYCDchr16:83933151chr20:61880247ENST00000262430+15491_4930494.0MotifMicrobody targeting signal
HgeneMLYCDchr16:83933151chr20:61880247ENST00000262430+15191_4930494.0RegionNote=Catalytic domain
HgeneMLYCDchr16:83933151chr20:61880247ENST00000262430+15299_3050494.0RegionMalonyl-CoA binding
HgeneMLYCDchr16:83933151chr20:61880247ENST00000262430+1540_1900494.0RegionNote=Alpha-helical domain
TgeneNKAIN4chr16:83933151chr20:61880247ENST000003703161735_5564.0209.0TransmembraneHelical


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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
MLYCD
NKAIN4


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 MLYCD-NKAIN4


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 MLYCD-NKAIN4


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