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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: 24513

FusionGeneSummary for NMT1_NME1

check button Fusion gene summary
Fusion gene informationFusion gene name: NMT1_NME1
Fusion gene ID: 24513
HgeneTgene
Gene symbol

NMT1

NME1

Gene ID

4836

6023

Gene nameN-myristoyltransferase 1RNA component of mitochondrial RNA processing endoribonuclease
SynonymsNMTCHH|NME1|RMRPR|RRP2
Cytomap

17q21.31

9p13.3

Type of geneprotein-codingncRNA
Descriptionglycylpeptide N-tetradecanoyltransferase 1alternative, short form NMT-Slong form, NMT-Lmyristoyl-CoA:protein N-myristoyltransferase 1type I N-myristoyltransferase-
Modification date2018052320180519
UniProtAcc

P30419

P15531

Ensembl transtripts involved in fusion geneENST00000592782, ENST00000258960, 
ENST00000590114, 
ENST00000393196, 
ENST00000336097, ENST00000480143, 
ENST00000511355, ENST00000013034, 
Fusion gene scores* DoF score6 X 5 X 4=1202 X 2 X 2=8
# samples 62
** MAII scorelog2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/8*10)=1.32192809488736
Context

PubMed: NMT1 [Title/Abstract] AND NME1 [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
HgeneNMT1

GO:0018008

N-terminal peptidyl-glycine N-myristoylation

25255805

HgeneNMT1

GO:0042180

cellular ketone metabolic process

22865860

TgeneNME1

GO:0001172

transcription, RNA-templated

19701182

TgeneNME1

GO:0030422

production of siRNA involved in RNA interference

19701182

TgeneNME1

GO:0032774

RNA biosynthetic process

19701182


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
TCGALDLUSCTCGA-43-2581-01ANMT1chr17

43138828

+NME1chr17

49233012

+
* 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-5UTRENST00000592782ENST00000393196NMT1chr17

43138828

+NME1chr17

49233012

+
5CDS-5UTRENST00000592782ENST00000336097NMT1chr17

43138828

+NME1chr17

49233012

+
5CDS-5UTRENST00000592782ENST00000480143NMT1chr17

43138828

+NME1chr17

49233012

+
5CDS-5UTRENST00000592782ENST00000511355NMT1chr17

43138828

+NME1chr17

49233012

+
5CDS-5UTRENST00000592782ENST00000013034NMT1chr17

43138828

+NME1chr17

49233012

+
5CDS-5UTRENST00000258960ENST00000393196NMT1chr17

43138828

+NME1chr17

49233012

+
5CDS-5UTRENST00000258960ENST00000336097NMT1chr17

43138828

+NME1chr17

49233012

+
5CDS-5UTRENST00000258960ENST00000480143NMT1chr17

43138828

+NME1chr17

49233012

+
5CDS-5UTRENST00000258960ENST00000511355NMT1chr17

43138828

+NME1chr17

49233012

+
5CDS-5UTRENST00000258960ENST00000013034NMT1chr17

43138828

+NME1chr17

49233012

+
3UTR-5UTRENST00000590114ENST00000393196NMT1chr17

43138828

+NME1chr17

49233012

+
3UTR-5UTRENST00000590114ENST00000336097NMT1chr17

43138828

+NME1chr17

49233012

+
3UTR-5UTRENST00000590114ENST00000480143NMT1chr17

43138828

+NME1chr17

49233012

+
3UTR-5UTRENST00000590114ENST00000511355NMT1chr17

43138828

+NME1chr17

49233012

+
3UTR-5UTRENST00000590114ENST00000013034NMT1chr17

43138828

+NME1chr17

49233012

+

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FusionProtFeatures for NMT1_NME1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NMT1

P30419

NME1

P15531

Adds a myristoyl group to the N-terminal glycine residueof certain cellular and viral proteins.{ECO:0000269|PubMed:25255805, ECO:0000269|PubMed:9353336,ECO:0000269|PubMed:9506952}. Major role in the synthesis of nucleoside triphosphatesother than ATP. The ATP gamma phosphate is transferred to the NDPbeta phosphate via a ping-pong mechanism, using a phosphorylatedactive-site intermediate. Possesses nucleoside-diphosphate kinase,serine/threonine-specific protein kinase, geranyl and farnesylpyrophosphate kinase, histidine protein kinase and 3'-5'exonuclease activities. Involved in cell proliferation,differentiation and development, signal transduction, G protein-coupled receptor endocytosis, and gene expression. Required forneural development including neural patterning and cell fatedetermination. During GZMA-mediated cell death, works in concertwith TREX1. NME1 nicks one strand of DNA and TREX1 removes basesfrom the free 3' end to enhance DNA damage and prevent DNA endreannealing and rapid repair. {ECO:0000269|PubMed:12628186,ECO:0000269|PubMed:16818237, ECO:0000269|PubMed:8810265}.

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 NMT1_NME1


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 NMT1_NME1


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
NMT1LYN, FYN, CABP2, CABP1, CSNK2A1, HNRNPM, HNRNPU, IARS, IGF2BP3, ILF2, MAP2, MRE11A, ABCF1, C14orf166, RTCB, NELFB, YBX3, DDX1, DHX9, DIMT1, DYNC1LI2, EDC4, EIF2B2, EIF2B3, FKBP3, FLII, PA2G4, POLR1C, QARS, RFC4, RPL19, RPL38, YBX1, PDCD6, RPL23A, NXF1, CAPN1, TP53, CDCA3, FBXO17, ODF3L2, FAM84B, PLCXD1, EID3, RP2, TGFB1, ABLIM1, DTNA, ZNRF1, ACSL4, MARS, NTRK1, AHI1, CEP89, FBF1, SCLT1, DCTN1, CEP19, STIL, VIM, NOP56, FBXW7, MCM2, GPRC5C, NCS1, MARCKSL1, AIFM3, TLDC1, ANGPTL7, MGST3, DEFB1, ANGPTL4, BAG4, RFTN2, TBCE, MLF1, DNAJC13, EDRF1, C1orf168, IRF2BP1NME1WDYHV1, NME4, POLR1C, GORASP2, NME3, NME1, SET, AURKA, TERF1, ITGB1, RRAD, TIAM1, RAC1, PRUNE, USP18, GATA1, STRAP, NME2, HDAC5, ERG, MIF, SOD1, UROD, FXR2, NIF3L1, CCND3, SMARCD1, SOX30, FBXO6, IDH1, CHRAC1, FDPS, MAPK14, NME1-NME2, OXCT1, SORD, THOP1, RBBP7, WDR1, ASB18, TUBG1, TNPO2, PID1, SREK1IP1, BMI1, CFL1, CRIP1, DYNLL1, FUBP1, GOT1, NQO1, PRDX5, PTEN, FBXO24, KAT2A, FOXP4, MCM2, DUSP19, DUSP2, DUSP22, EYA2, EYA3, DNM1L, SOAT1, FOXA1, BRCA1


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 NMT1_NME1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneNME1P15531DB01593ZincNucleoside diphosphate kinase Asmall moleculeapproved|investigational

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RelatedDiseases for NMT1_NME1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneNME1C0007194Hypertrophic Cardiomyopathy1CTD_human
TgeneNME1C0009404Colorectal Neoplasms1CTD_human
TgeneNME1C0027626Neoplasm Invasiveness1CTD_human
TgeneNME1C0027627Neoplasm Metastasis1CTD_human
TgeneNME1C0242184Hypoxia1CTD_human
TgeneNME1C2239176Liver carcinoma1CTD_human