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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 16625

FusionGeneSummary for HNRNPM_SLC25A23

check button Fusion gene summary
Fusion gene informationFusion gene name: HNRNPM_SLC25A23
Fusion gene ID: 16625
HgeneTgene
Gene symbol

HNRNPM

SLC25A23

Gene ID

4670

79085

Gene nameheterogeneous nuclear ribonucleoprotein Msolute carrier family 25 member 23
SynonymsCEAR|HNRNPM4|HNRPM|HNRPM4|HTGR1|NAGR1|hnRNP MAPC2|MCSC2|SCaMC-3
Cytomap

19p13.2

19p13.3

Type of geneprotein-codingprotein-coding
Descriptionheterogeneous nuclear ribonucleoprotein MCEA receptorN-acetylglucosamine receptor 1heterogenous nuclear ribonucleoprotein M4hnRNA-binding protein M4calcium-binding mitochondrial carrier protein SCaMC-3mitochondrial ATP-Mg/Pi carrier protein 2mitochondrial Ca(2+)-dependent solute carrier protein 2mitochondrial Ca2+-dependent solute carrier protein 2short calcium-binding mitochondrial carrier 3sma
Modification date2018052320180523
UniProtAcc

P52272

Q9BV35

Ensembl transtripts involved in fusion geneENST00000348943, ENST00000325495, 
ENST00000602219, 
ENST00000601760, 
ENST00000301454, ENST00000414491, 
ENST00000334510, 
Fusion gene scores* DoF score12 X 10 X 8=9602 X 2 X 2=8
# samples 132
** MAII scorelog2(13/960*10)=-2.88452278258006
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: HNRNPM [Title/Abstract] AND SLC25A23 [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
TCGARVLUADTCGA-75-5125-01AHNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
* 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
5CDS-intronENST00000348943ENST00000601760HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
5CDS-intronENST00000348943ENST00000301454HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
5CDS-intronENST00000348943ENST00000414491HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
5CDS-intronENST00000348943ENST00000334510HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
5CDS-intronENST00000325495ENST00000601760HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
5CDS-intronENST00000325495ENST00000301454HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
5CDS-intronENST00000325495ENST00000414491HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
5CDS-intronENST00000325495ENST00000334510HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
intron-intronENST00000602219ENST00000601760HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
intron-intronENST00000602219ENST00000301454HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
intron-intronENST00000602219ENST00000414491HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-
intron-intronENST00000602219ENST00000334510HNRNPMchr19

8509995

+SLC25A23chr19

6438545

-

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FusionProtFeatures for HNRNPM_SLC25A23


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

P52272

SLC25A23

Q9BV35

Pre-mRNA binding protein in vivo, binds avidly topoly(G) and poly(U) RNA homopolymers in vitro. Involved insplicing. Acts as a receptor for carcinoembryonic antigen inKupffer cells, may initiate a series of signaling events leadingto tyrosine phosphorylation of proteins and induction of IL-1alpha, IL-6, IL-10 and tumor necrosis factor alpha cytokines. Calcium-dependent mitochondrial solute carrier.Mitochondrial solute carriers shuttle metabolites, nucleotides,and cofactors through the mitochondrial inner membrane(PubMed:15123600). May act as a ATP-Mg/Pi exchanger that mediatesthe transport of Mg-ATP in exchange for phosphate, catalyzing thenet uptake or efflux of adenine nucleotides into or from themitochondria (PubMed:15123600). Acts as a regulator ofmitochondrial calcium uptake via interaction with MCU and MICU1(PubMed:24430870). {ECO:0000269|PubMed:15123600,ECO:0000269|PubMed:24430870}.

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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FusionGeneSequence for HNRNPM_SLC25A23


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).

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FusionGenePPI for HNRNPM_SLC25A23


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
HNRNPMPRRC2A, RBM4B, LMO3, TCERG1, GSTK1, PHLDA3, RFXANK, PTP4A3, TSC22D1, JUN, LYST, HNRNPA1, HNRNPH1, APC, SRRM1, SRRM2, TOPORS, MORF4L1, MORF4L2, MRGBP, DOT1L, NPM1, TADA2A, UBC, NOP56, VHL, SMARCAD1, ARRB1, ARRB2, ERG, KIAA0368, NFX1, CUL3, CUL2, CDK2, CUL1, COPS5, CAND1, PRAME, FBXO6, RBM8A, U2AF2, PRPF6, EFTUD2, NHP2L1, SNRPD1, RBMX, SF3B3, SF3A1, SNRPA1, SF3B1, U2AF1, HNRNPC, SNRPD3, SRSF1, HNRNPF, ALYREF, HNRNPR, HNRNPK, PRPF8, RNPS1, SRSF5, SRSF3, SYNCRIP, SFPQ, NONO, RBM25, HNRNPA0, HNRNPL, RPL10A, RPS6, RPL7, RALY, RPS24, RPS8, RPL11, RPL23A, RPS23, RPL7A, RPL12, DDX5, RPL31, RPS13, RPL6, RPL14, RPS15A, RPS16, RPLP0, DDX1, RPL18, RPL5, RPS11, TOP1, RPS7, RPS2, RPS14, PRPF19, RPL10, RPL19, RPL23, HNRNPDL, RPL18A, RPL30, RPL22, PUF60, RPS26, SRRT, RPS4X, PRPF40A, RPSA, RPS21, PRPF3, RPS5, RPS28, RPS25, RBM14, SND1, RANBP2, MRPL37, KRT16, STOM, MBD3, UQCR10, SLC25A24, SUPT16H, RPLP0P6, RRBP1, VTN, RCC1, RRS1, ZNF326, PCDHA2, LMNA, SMC3, SON, TRA2A, RAB31, RTN4, SMARCA5, LMNB1, MRPL55, MYH10, RAP1A, SSR1, FLNB, THRAP3, RRP7A, SEPT2, MRPS28, TOR1AIP1, SAMM50, TOMM70A, RCC2, ADAR, DHODH, MRPL23, MRPS9, TIMM9, MTA2, GTF3C1, ESR1, MAGOH, EIF4A3, FN1, VCAM1, ZNF207, RBM4, WDR77, MAP1LC3A, UBL4A, ITGA4, CTNNB1, AICDA, PAN2, CD81, IGSF8, LMO2, STAT3, SRPK2, CLK2, SRPK3, TARDBP, PARK2, ABCF1, RTCB, DHX9, EIF2B2, EIF2B3, FLII, IGF2BP3, NMT1, PSMB8, RFC4, RPL26L1, RPL27, MRE11A, RPA1, RPA2, RPA3, CDC37, IVNS1ABP, STAU1, MDM2, HAUS1, CEP250, TP53, AKAP9, GMCL1P1, TEKT4, ENO1, SHMT2, MOV10, NXF1, UBE2I, EED, ERLIN2, UBAC2, ABL1, ILK, MAST3, SRPK1, PLRG1, CDC5L, RPS6KB2, NTRK1, LRRC59, UQCRC2, SFN, SCARNA22, B9D2, XPO1, HNRNPH2, MATR3, SEC16A, MYEF2, GAN, SKI, CRY2, MCM2, SNW1, CRBN, C11orf30, ZNF746, CYLD, SMARCB1, BRCA1, RNF168, MTF1SLC25A23ELAVL1, CUL3, TARDBP, APPBP2, NRG1, SLC25A25, IL13RA2, SYP, CD79B, PDCD1, SLC22A6, SLC2A12, AIFM1, APLNR, VSIG4, TMEM108, SLC5A8, LRP1


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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RelatedDrugs for HNRNPM_SLC25A23


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

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RelatedDiseases for HNRNPM_SLC25A23


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