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Fusion gene ID: 22723 |
FusionGeneSummary for MTCH2_FHIT |
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Fusion gene information | Fusion gene name: MTCH2_FHIT | Fusion gene ID: 22723 | Hgene | Tgene | Gene symbol | MTCH2 | FHIT | Gene ID | 23788 | 2272 |
Gene name | mitochondrial carrier 2 | fragile histidine triad | |
Synonyms | HSPC032|MIMP|SLC25A50 | AP3Aase|FRA3B | |
Cytomap | 11p11.2 | 3p14.2 | |
Type of gene | protein-coding | protein-coding | |
Description | mitochondrial carrier homolog 22310034D24Rikmet-induced mitochondrial proteinsolute carrier family 25, member 50 | bis(5'-adenosyl)-triphosphataseAP3A hydrolasediadenosine 5',5'''-P1,P3-triphosphate hydrolasedinucleosidetriphosphatase | |
Modification date | 20180523 | 20180519 | |
UniProtAcc | Q9Y6C9 | P49789 | |
Ensembl transtripts involved in fusion gene | ENST00000302503, ENST00000542981, ENST00000534074, | ENST00000476844, ENST00000492590, ENST00000466788, ENST00000468189, ENST00000341848, | |
Fusion gene scores | * DoF score | 6 X 4 X 4=96 | 17 X 7 X 10=1190 |
# samples | 6 | 20 | |
** MAII score | log2(6/96*10)=-0.678071905112638 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(20/1190*10)=-2.57288966842058 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: MTCH2 [Title/Abstract] AND FHIT [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation | Tumor suppressor gene involved fusion gene, in-frame but not retained their domain. Tumor suppressor gene involved fusion gene, retained protein feature but frameshift. DDR (DNA damage repair) gene involved fusion gene, in-frame but not retained their domain. |
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types ** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | FHIT | GO:0006163 | purine nucleotide metabolic process | 9323207 |
![]() (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 type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
TCGA | RV | OV | TCGA-23-2077-01A | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
In-frame | ENST00000302503 | ENST00000476844 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
In-frame | ENST00000302503 | ENST00000492590 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
5CDS-5UTR | ENST00000302503 | ENST00000466788 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
5CDS-5UTR | ENST00000302503 | ENST00000468189 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
5CDS-5UTR | ENST00000302503 | ENST00000341848 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
5UTR-3CDS | ENST00000542981 | ENST00000476844 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
5UTR-3CDS | ENST00000542981 | ENST00000492590 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
5UTR-5UTR | ENST00000542981 | ENST00000466788 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
5UTR-5UTR | ENST00000542981 | ENST00000468189 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
5UTR-5UTR | ENST00000542981 | ENST00000341848 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
intron-3CDS | ENST00000534074 | ENST00000476844 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
intron-3CDS | ENST00000534074 | ENST00000492590 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
intron-5UTR | ENST00000534074 | ENST00000466788 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
intron-5UTR | ENST00000534074 | ENST00000468189 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
intron-5UTR | ENST00000534074 | ENST00000341848 | MTCH2 | chr11 | 47660251 | - | FHIT | chr3 | 59738047 | - |
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FusionProtFeatures for MTCH2_FHIT |
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Hgene | Tgene |
MTCH2 | FHIT |
The substrate transported is not yet known. Inducesmitochondrial depolarization. | Cleaves P(1)-P(3)-bis(5'-adenosyl) triphosphate (Ap3A)to yield AMP and ADP. Can also hydrolyze P(1)-P(4)-bis(5'-adenosyl) tetraphosphate (Ap4A), but has extremely low activitywith ATP. Modulates transcriptional activation by CTNNB1 andthereby contributes to regulate the expression of genes essentialfor cell proliferation and survival, such as CCND1 and BIRC5.Plays a role in the induction of apoptosis via SRC and AKT1signaling pathways. Inhibits MDM2-mediated proteasomal degradationof p53/TP53 and thereby plays a role in p53/TP53-mediatedapoptosis. Induction of apoptosis depends on the ability of FHITto bind P(1)-P(3)-bis(5'-adenosyl) triphosphate or relatedcompounds, but does not require its catalytic activity, it may inpart come from the mitochondrial form, which sensitizes the low-affinity Ca(2+) transporters, enhancing mitochondrial calciumuptake. Functions as tumor suppressor.{ECO:0000269|PubMed:12574506, ECO:0000269|PubMed:15313915,ECO:0000269|PubMed:16407838, ECO:0000269|PubMed:18077326,ECO:0000269|PubMed:19622739, ECO:0000269|PubMed:8794732,ECO:0000269|PubMed:9323207}. |
![]() * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | MTCH2 | chr11:47660251 | chr3:59738047 | ENST00000302503 | - | 3 | 13 | 8_28 | 93 | 304 | Transmembrane | Helical |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | >MTCH2 | chr11:47660251 | chr3:59738047 | ENST00000302503 | - | 3 | 13 | 118_206 | 93 | 304 | Repeat | Note=Solcar 2 |
Hgene | >MTCH2 | chr11:47660251 | chr3:59738047 | ENST00000302503 | - | 3 | 13 | 2_98 | 93 | 304 | Repeat | Note=Solcar 1 |
Hgene | >MTCH2 | chr11:47660251 | chr3:59738047 | ENST00000302503 | - | 3 | 13 | 175_195 | 93 | 304 | Transmembrane | Helical |
Hgene | >MTCH2 | chr11:47660251 | chr3:59738047 | ENST00000302503 | - | 3 | 13 | 224_244 | 93 | 304 | Transmembrane | Helical |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000341848 | - | 3 | 5 | 2_109 | 116 | 148 | Domain | HIT |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000468189 | - | 7 | 9 | 2_109 | 116 | 148 | Domain | HIT |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000476844 | - | 7 | 10 | 2_109 | 116 | 214 | Domain | HIT |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000492590 | - | 7 | 10 | 2_109 | 116 | 205 | Domain | HIT |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000341848 | - | 3 | 5 | 94_98 | 116 | 148 | Motif | Histidine triad motif |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000468189 | - | 7 | 9 | 94_98 | 116 | 148 | Motif | Histidine triad motif |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000476844 | - | 7 | 10 | 94_98 | 116 | 214 | Motif | Histidine triad motif |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000492590 | - | 7 | 10 | 94_98 | 116 | 205 | Motif | Histidine triad motif |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000341848 | - | 3 | 5 | 89_92 | 116 | 148 | Nucleotide binding | Substrate |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000468189 | - | 7 | 9 | 89_92 | 116 | 148 | Nucleotide binding | Substrate |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000476844 | - | 7 | 10 | 89_92 | 116 | 214 | Nucleotide binding | Substrate |
Tgene | FHIT | chr11:47660251 | chr3:59738047 | ENST00000492590 | - | 7 | 10 | 89_92 | 116 | 205 | Nucleotide binding | Substrate |
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FusionGeneSequence for MTCH2_FHIT |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
>In-frame_MTCH2_ENST00000302503_chr11_47660251_-_FHIT_ENST00000476844_chr3_59738047_-_125aa MADAASQVLLGSGLTILSQPLMYVKVLIQVGYEPLPPTIGRNIFGRQVCQLPGLFSYAQHIASIDGRRGLFTGLTPRLCSGVLGTVVHGK >In-frame_MTCH2_ENST00000302503_chr11_47660251_-_FHIT_ENST00000492590_chr3_59738047_-_125aa MADAASQVLLGSGLTILSQPLMYVKVLIQVGYEPLPPTIGRNIFGRQVCQLPGLFSYAQHIASIDGRRGLFTGLTPRLCSGVLGTVVHGK |
* Fusion transcript sequences (only coding sequence (CDS) region). |
>In-frame_MTCH2_ENST00000302503_chr11_47660251_-_FHIT_ENST00000476844_chr3_59738047_-_375nt ATGGCGGACGCGGCCAGTCAGGTGCTCCTGGGCTCCGGTCTCACCATCCTGTCCCAGCCGCTCATGTACGTGAAAGTGCTCATCCAGGTG GGATATGAGCCTCTTCCTCCAACAATAGGACGAAATATTTTTGGGCGGCAAGTGTGTCAGCTTCCTGGTCTCTTTAGTTATGCTCAGCAC ATTGCCAGTATCGATGGGAGGCGCGGGTTGTTCACAGGCTTAACTCCAAGACTGTGTTCGGGAGTCCTTGGAACTGTGGTCCATGGTAAA GTTTTACAGCTCCAGAAACATGACAAGGAGGACTTTCCTGCCTCTTGGAGATCAGAGGAGGAAATGGCAGCAGAAGCCGCAGCTCTGCGG >In-frame_MTCH2_ENST00000302503_chr11_47660251_-_FHIT_ENST00000492590_chr3_59738047_-_375nt ATGGCGGACGCGGCCAGTCAGGTGCTCCTGGGCTCCGGTCTCACCATCCTGTCCCAGCCGCTCATGTACGTGAAAGTGCTCATCCAGGTG GGATATGAGCCTCTTCCTCCAACAATAGGACGAAATATTTTTGGGCGGCAAGTGTGTCAGCTTCCTGGTCTCTTTAGTTATGCTCAGCAC ATTGCCAGTATCGATGGGAGGCGCGGGTTGTTCACAGGCTTAACTCCAAGACTGTGTTCGGGAGTCCTTGGAACTGTGGTCCATGGTAAA GTTTTACAGCTCCAGAAACATGACAAGGAGGACTTTCCTGCCTCTTGGAGATCAGAGGAGGAAATGGCAGCAGAAGCCGCAGCTCTGCGG |
* Fusion transcript sequences (Full-length transcript). |
>In-frame_MTCH2_ENST00000302503_chr11_47660251_-_FHIT_ENST00000476844_chr3_59738047_-_797nt GGGGCGGGGACTGGGCGGAGAGGCGCGTGCTGCTGCGTGCGTGCGCGCGCGCCGCGGGCGGGCCAGTGAAACCGGCGGCCCTGGCACGTG ACCTAGGACCGGCTCACCGGGTCGCTTGGTGGCTCCGTCTGTCTGTCCGTCCGCCCGCGGGTGCCATCATGGCGGACGCGGCCAGTCAGG TGCTCCTGGGCTCCGGTCTCACCATCCTGTCCCAGCCGCTCATGTACGTGAAAGTGCTCATCCAGGTGGGATATGAGCCTCTTCCTCCAA CAATAGGACGAAATATTTTTGGGCGGCAAGTGTGTCAGCTTCCTGGTCTCTTTAGTTATGCTCAGCACATTGCCAGTATCGATGGGAGGC GCGGGTTGTTCACAGGCTTAACTCCAAGACTGTGTTCGGGAGTCCTTGGAACTGTGGTCCATGGTAAAGTTTTACAGCTCCAGAAACATG ACAAGGAGGACTTTCCTGCCTCTTGGAGATCAGAGGAGGAAATGGCAGCAGAAGCCGCAGCTCTGCGGGTCTACTTTCAGTGACACAGAT CCTGAATTCCAGCAAAAGAGCTATTGCCAACCAGTTTGAAGACCGCCCCCCGCCTCTCCCCAAGAGGAACTGAATCAGCATGAAAATGCA GTTTCTTCATCTCACCATCCTGTATTCTTCAACCAGTGATCCCCCACCTCGGTCACTCCAACTCCCTTAAAATACCTAGACCTAAACGGC >In-frame_MTCH2_ENST00000302503_chr11_47660251_-_FHIT_ENST00000492590_chr3_59738047_-_808nt GGGGCGGGGACTGGGCGGAGAGGCGCGTGCTGCTGCGTGCGTGCGCGCGCGCCGCGGGCGGGCCAGTGAAACCGGCGGCCCTGGCACGTG ACCTAGGACCGGCTCACCGGGTCGCTTGGTGGCTCCGTCTGTCTGTCCGTCCGCCCGCGGGTGCCATCATGGCGGACGCGGCCAGTCAGG TGCTCCTGGGCTCCGGTCTCACCATCCTGTCCCAGCCGCTCATGTACGTGAAAGTGCTCATCCAGGTGGGATATGAGCCTCTTCCTCCAA CAATAGGACGAAATATTTTTGGGCGGCAAGTGTGTCAGCTTCCTGGTCTCTTTAGTTATGCTCAGCACATTGCCAGTATCGATGGGAGGC GCGGGTTGTTCACAGGCTTAACTCCAAGACTGTGTTCGGGAGTCCTTGGAACTGTGGTCCATGGTAAAGTTTTACAGCTCCAGAAACATG ACAAGGAGGACTTTCCTGCCTCTTGGAGATCAGAGGAGGAAATGGCAGCAGAAGCCGCAGCTCTGCGGGTCTACTTTCAGTGACACAGAT GTTTTTCAGATCCTGAATTCCAGCAAAAGAGCTATTGCCAACCAGTTTGAAGACCGCCCCCCGCCTCTCCCCAAGAGGAACTGAATCAGC ATGAAAATGCAGTTTCTTCATCTCACCATCCTGTATTCTTCAACCAGTGATCCCCCACCTCGGTCACTCCAACTCCCTTAAAATACCTAG |
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FusionGenePPI for MTCH2_FHIT |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
MTCH2 | UBC, 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, PDHA1 | FHIT | FHIT, UBE2I, CTNNB1, LEF1, TRIM23, RAB40B, MDM2, REL, TP53, ARHGAP19, MTMR6, RABL2A, CHEK1 |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for MTCH2_FHIT |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | FHIT | P49789 | DB04173 | Fructose | Bis(5'-adenosyl)-triphosphatase | small molecule | approved|experimental |
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RelatedDiseases for MTCH2_FHIT |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | MTCH2 | C0028754 | Obesity | 1 | CTD_human |
Tgene | FHIT | C0024121 | Lung Neoplasms | 2 | CTD_human |
Tgene | FHIT | C0025500 | Mesothelioma | 2 | CTD_human |
Tgene | FHIT | C0007131 | Non-Small Cell Lung Carcinoma | 1 | CTD_human |
Tgene | FHIT | C0023903 | Liver neoplasms | 1 | CTD_human |
Tgene | FHIT | C0033578 | Prostatic Neoplasms | 1 | CTD_human |
Tgene | FHIT | C0036341 | Schizophrenia | 1 | PSYGENET |
Tgene | FHIT | C0038356 | Stomach Neoplasms | 1 | CTD_human |
Tgene | FHIT | C0042076 | Urologic Neoplasms | 1 | CTD_human |
Tgene | FHIT | C0236733 | Amphetamine-Related Disorders | 1 | CTD_human |
Tgene | FHIT | C0236969 | Substance-Related Disorders | 1 | CTD_human |