FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 22722

FusionGeneSummary for MTCH2_AGBL2

check button Fusion gene summary
Fusion gene informationFusion gene name: MTCH2_AGBL2
Fusion gene ID: 22722
HgeneTgene
Gene symbol

MTCH2

AGBL2

Gene ID

23788

79841

Gene namemitochondrial carrier 2ATP/GTP binding protein like 2
SynonymsHSPC032|MIMP|SLC25A50CCP2
Cytomap

11p11.2

11p11.2

Type of geneprotein-codingprotein-coding
Descriptionmitochondrial carrier homolog 22310034D24Rikmet-induced mitochondrial proteinsolute carrier family 25, member 50cytosolic carboxypeptidase 2cytoplasmic carboxypeptidase 2testis tissue sperm-binding protein Li 96mP
Modification date2018052320180519
UniProtAcc

Q9Y6C9

Q5U5Z8

Ensembl transtripts involved in fusion geneENST00000302503, ENST00000542981, 
ENST00000534074, 
ENST00000525123, 
ENST00000298861, ENST00000357610, 
ENST00000528244, ENST00000529712, 
Fusion gene scores* DoF score6 X 4 X 4=962 X 2 X 1=4
# samples 62
** MAII scorelog2(6/96*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: MTCH2 [Title/Abstract] AND AGBL2 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotation
* 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

check button Fusion gene information from three resources
(ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018))
* 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.
Data typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDOVTCGA-09-1666-01AMTCH2chr11

47660251

-AGBL2chr11

47681898

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
In-frameENST00000302503ENST00000525123MTCH2chr11

47660251

-AGBL2chr11

47681898

-
Frame-shiftENST00000302503ENST00000298861MTCH2chr11

47660251

-AGBL2chr11

47681898

-
Frame-shiftENST00000302503ENST00000357610MTCH2chr11

47660251

-AGBL2chr11

47681898

-
5CDS-intronENST00000302503ENST00000528244MTCH2chr11

47660251

-AGBL2chr11

47681898

-
5CDS-intronENST00000302503ENST00000529712MTCH2chr11

47660251

-AGBL2chr11

47681898

-
5UTR-3CDSENST00000542981ENST00000525123MTCH2chr11

47660251

-AGBL2chr11

47681898

-
5UTR-3CDSENST00000542981ENST00000298861MTCH2chr11

47660251

-AGBL2chr11

47681898

-
5UTR-3CDSENST00000542981ENST00000357610MTCH2chr11

47660251

-AGBL2chr11

47681898

-
5UTR-intronENST00000542981ENST00000528244MTCH2chr11

47660251

-AGBL2chr11

47681898

-
5UTR-intronENST00000542981ENST00000529712MTCH2chr11

47660251

-AGBL2chr11

47681898

-
intron-3CDSENST00000534074ENST00000525123MTCH2chr11

47660251

-AGBL2chr11

47681898

-
intron-3CDSENST00000534074ENST00000298861MTCH2chr11

47660251

-AGBL2chr11

47681898

-
intron-3CDSENST00000534074ENST00000357610MTCH2chr11

47660251

-AGBL2chr11

47681898

-
intron-intronENST00000534074ENST00000528244MTCH2chr11

47660251

-AGBL2chr11

47681898

-
intron-intronENST00000534074ENST00000529712MTCH2chr11

47660251

-AGBL2chr11

47681898

-

Top

FusionProtFeatures for MTCH2_AGBL2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MTCH2

Q9Y6C9

AGBL2

Q5U5Z8

The substrate transported is not yet known. Inducesmitochondrial depolarization. Metallocarboxypeptidase that mediates deglutamylation oftarget proteins. Catalyzes the deglutamylation of polyglutamateside chains generated by post-translational polyglutamylation inproteins such as tubulins. Also removes gene-encodedpolyglutamates from the carboxy-terminus of target proteins suchas MYLK. Does not show detyrosinase or deglycylase activities fromthe carboxy-terminus of tubulin. {ECO:0000250|UniProtKB:Q8CDK2,ECO:0000269|PubMed:21303978}.

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
HgeneMTCH2chr11:47660251chr11:47681898ENST00000302503-3138_2893304TransmembraneHelical

- In-frame and not-retained protein feature among the 13 regional features.
>>>>
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneMTCH2chr11:47660251chr11:47681898ENST00000302503-313118_20693304RepeatNote=Solcar 2
HgeneMTCH2chr11:47660251chr11:47681898ENST00000302503-3132_9893304RepeatNote=Solcar 1
HgeneMTCH2chr11:47660251chr11:47681898ENST00000302503-313175_19593304TransmembraneHelical
HgeneMTCH2chr11:47660251chr11:47681898ENST00000302503-313224_24493304TransmembraneHelical


Top

FusionGeneSequence for MTCH2_AGBL2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(nt: nucleotides, aa: amino acids)

* Fusion amino acid sequences.

* Fusion transcript sequences (only coding sequence (CDS) region).

* Fusion transcript sequences (Full-length transcript).

Top

FusionGenePPI for MTCH2_AGBL2


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
MTCH2UBC, ESR1, HNRNPU, FMNL1, XRN1, FBXO6, RNF2, RIC3, HCCS, CACNG2, SUCNR1, LYPD3, PLIN3, WNT4, SLC38A6, FAM219B, NTRK1, ALDH3A2, ATP1A1, ATP2A2, ATP5C1, ATP6V0D1, CLTC, GNAI2, MRPL37, ATP1B1, ATP1B3, ATP5A1, ATP5B, ATP5F1, ATP5L, ATP5O, LMAN1, NDUFB5, SLC25A3, TOMM40, NDUFA12, NDUFA2, NDUFA6, NDUFB8, NDUFB9, NDUFS1, NDUFS2, NDUFS3, PHB, PHB2, RAB1A, RPN1, SDHB, SDHC, SGPL1, TOMM22, UQCRC2, VDAC1, VDAC2, VDAC3, OFD1, MCM2, UBXN8, COQ9, NDUFA4, CHCHD10, C15orf48, OCIAD1, PTPMT1, OPA3, ADCK1, APOOL, GLP1R, DUSP21, DUSP22, DUSP23, DUSP4, SLC7A1, IMPDH1, CD97, CD44, PVR, TMEM206, VAC14, SPPL2B, BCAM, SLC1A5, PTPN5, PDHA1AGBL2TP53, TP63, TP73, TPM2


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


Top

RelatedDrugs for MTCH2_AGBL2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

RelatedDiseases for MTCH2_AGBL2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMTCH2C0028754Obesity1CTD_human