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Center for Computational Systems Medicine level2
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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 Structure

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pLDDT scores

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Ramachandran Plot of Fusion Protein Structure

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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:NAA15-LPAR1

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NAA15-LPAR1
FusionPDB ID: 56943
FusionGDB2.0 ID: 56943
HgeneTgene
Gene symbol

NAA15

LPAR1

Gene ID

80155

1902

Gene nameN-alpha-acetyltransferase 15, NatA auxiliary subunitlysophosphatidic acid receptor 1
SynonymsGa19|MRD50|NARG1|NAT1P|NATH|TBDN|TBDN100EDG2|GPR26|Gpcr26|LPA1|Mrec1.3|VZG1|edg-2|rec.1.3|vzg-1
Cytomap

4q31.1

9q31.3

Type of geneprotein-codingprotein-coding
DescriptionN-alpha-acetyltransferase 15, NatA auxiliary subunitN-terminal acetyltransferaseNMDA receptor regulated 1NMDA receptor-regulated protein 1gastric cancer antigen Ga19protein tubedown-1transcriptional coactivator tubedown-100tubedown-1lysophosphatidic acid receptor 1LPA receptor 1LPA-1endothelial differentiation, lysophosphatidic acid G-protein-coupled receptor, 2lysophosphatidic acid receptor Edg-2ventricular zone gene 1
Modification date2020031320200313
UniProtAcc

Q9BXJ9

Q92633

Ensembl transtripts involved in fusion geneENST idsENST00000296543, ENST00000398947, 
ENST00000480277, ENST00000515576, 
ENST00000358883, ENST00000374430, 
ENST00000374431, ENST00000538760, 
ENST00000541779, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 10 X 7=126010 X 6 X 6=360
# samples 2111
** MAII scorelog2(21/1260*10)=-2.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/360*10)=-1.71049338280502
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: NAA15 [Title/Abstract] AND LPAR1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NAA15(140222985)-LPAR1(113638002), # samples:3
Anticipated loss of major functional domain due to fusion event.NAA15-LPAR1 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.
NAA15-LPAR1 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.
NAA15-LPAR1 seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
NAA15-LPAR1 seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
NAA15-LPAR1 seems lost the major protein functional domain in Tgene partner, which is a IUPHAR drug target due to the frame-shifted 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
HgeneNAA15

GO:0006474

N-terminal protein amino acid acetylation

15496142

HgeneNAA15

GO:0045893

positive regulation of transcription, DNA-templated

12145306

TgeneLPAR1

GO:0007202

activation of phospholipase C activity

19306925


check buttonFusion gene breakpoints across NAA15 (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 LPAR1 (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
ChimerDB4GBMTCGA-06-0129-01ANAA15chr4

140222985

-LPAR1chr9

113638002

-
ChimerDB4GBMTCGA-06-0129-01ANAA15chr4

140222985

+LPAR1chr9

113638002

-
ChimerDB4GBMTCGA-06-0129NAA15chr4

140222985

+LPAR1chr9

113638002

-


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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)
ENST00000296543NAA15chr4140222985+ENST00000541779LPAR1chr9113638002-2836377277678133
ENST00000296543NAA15chr4140222985+ENST00000538760LPAR1chr9113638002-924377277678133
ENST00000398947NAA15chr4140222985+ENST00000541779LPAR1chr9113638002-2703244144545133
ENST00000398947NAA15chr4140222985+ENST00000538760LPAR1chr9113638002-791244144545133

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
ENST00000296543ENST00000541779NAA15chr4140222985+LPAR1chr9113638002-0.648310360.35168967
ENST00000296543ENST00000538760NAA15chr4140222985+LPAR1chr9113638002-0.373047950.626952
ENST00000398947ENST00000541779NAA15chr4140222985+LPAR1chr9113638002-0.485400620.5145994
ENST00000398947ENST00000538760NAA15chr4140222985+LPAR1chr9113638002-0.246405780.75359416

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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

>56943_56943_1_NAA15-LPAR1_NAA15_chr4_140222985_ENST00000296543_LPAR1_chr9_113638002_ENST00000538760_length(amino acids)=133AA_BP=33
MTEPGGGGSSGSSRNDAGREPPAQGECALQADLGAFIICWTPGLVLLLLDVCCPQCDVLAYEKFFLLLAEFNSAMNPIIYSYRDKEMSAT

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

>56943_56943_2_NAA15-LPAR1_NAA15_chr4_140222985_ENST00000296543_LPAR1_chr9_113638002_ENST00000541779_length(amino acids)=133AA_BP=33
MTEPGGGGSSGSSRNDAGREPPAQGECALQADLGAFIICWTPGLVLLLLDVCCPQCDVLAYEKFFLLLAEFNSAMNPIIYSYRDKEMSAT

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

>56943_56943_3_NAA15-LPAR1_NAA15_chr4_140222985_ENST00000398947_LPAR1_chr9_113638002_ENST00000538760_length(amino acids)=133AA_BP=33
MTEPGGGGSSGSSRNDAGREPPAQGECALQADLGAFIICWTPGLVLLLLDVCCPQCDVLAYEKFFLLLAEFNSAMNPIIYSYRDKEMSAT

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

>56943_56943_4_NAA15-LPAR1_NAA15_chr4_140222985_ENST00000398947_LPAR1_chr9_113638002_ENST00000541779_length(amino acids)=133AA_BP=33
MTEPGGGGSSGSSRNDAGREPPAQGECALQADLGAFIICWTPGLVLLLLDVCCPQCDVLAYEKFFLLLAEFNSAMNPIIYSYRDKEMSAT

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

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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/chr4:140222985/chr9:113638002)
- 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
NAA15

Q9BXJ9

LPAR1

Q92633

FUNCTION: Auxillary subunit of the N-terminal acetyltransferase A (NatA) complex which displays alpha (N-terminal) acetyltransferase activity. The NAT activity may be important for vascular, hematopoietic and neuronal growth and development. Required to control retinal neovascularization in adult ocular endothelial cells. In complex with XRCC6 and XRCC5 (Ku80), up-regulates transcription from the osteocalcin promoter. {ECO:0000269|PubMed:11687548, ECO:0000269|PubMed:12145306, ECO:0000269|PubMed:15496142}.FUNCTION: Receptor for lysophosphatidic acid (LPA) (PubMed:9070858, PubMed:19306925, PubMed:25025571, PubMed:26091040). Plays a role in the reorganization of the actin cytoskeleton, cell migration, differentiation and proliferation, and thereby contributes to the responses to tissue damage and infectious agents. Activates downstream signaling cascades via the G(i)/G(o), G(12)/G(13), and G(q) families of heteromeric G proteins. Signaling inhibits adenylyl cyclase activity and decreases cellular cAMP levels (PubMed:26091040). Signaling triggers an increase of cytoplasmic Ca(2+) levels (PubMed:19656035, PubMed:19733258, PubMed:26091040). Activates RALA; this leads to the activation of phospholipase C (PLC) and the formation of inositol 1,4,5-trisphosphate (PubMed:19306925). Signaling mediates activation of down-stream MAP kinases (By similarity). Contributes to the regulation of cell shape. Promotes Rho-dependent reorganization of the actin cytoskeleton in neuronal cells and neurite retraction (PubMed:26091040). Promotes the activation of Rho and the formation of actin stress fibers (PubMed:26091040). Promotes formation of lamellipodia at the leading edge of migrating cells via activation of RAC1 (By similarity). Through its function as lysophosphatidic acid receptor, plays a role in chemotaxis and cell migration, including responses to injury and wounding (PubMed:18066075, PubMed:19656035, PubMed:19733258). Plays a role in triggering inflammation in response to bacterial lipopolysaccharide (LPS) via its interaction with CD14. Promotes cell proliferation in response to lysophosphatidic acid. Required for normal skeleton development. May play a role in osteoblast differentiation. Required for normal brain development. Required for normal proliferation, survival and maturation of newly formed neurons in the adult dentate gyrus. Plays a role in pain perception and in the initiation of neuropathic pain (By similarity). {ECO:0000250|UniProtKB:P61793, ECO:0000269|PubMed:18066075, ECO:0000269|PubMed:19306925, ECO:0000269|PubMed:19656035, ECO:0000269|PubMed:19733258, ECO:0000269|PubMed:25025571, ECO:0000269|PubMed:26091040, ECO:0000269|PubMed:9070858, ECO:0000305|PubMed:11093753, ECO:0000305|PubMed:9069262}.

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
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324281_294264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324316_364264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035281_294264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035316_364264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135281_294264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135316_364264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324295_315264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D7
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035295_315264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D7
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135295_315264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D7

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+120629_63218.0867.0Compositional biasNote=Poly-Asp
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+120612_62918.0867.0MotifBipartite nuclear localization signal
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+120148_18418.0867.0RepeatNote=TPR 3
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+120224_25718.0867.0RepeatNote=TPR 4
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+120374_40718.0867.0RepeatNote=TPR 5
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+120409_44118.0867.0RepeatNote=TPR 6
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+12046_7918.0867.0RepeatNote=TPR 1
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+120485_51818.0867.0RepeatNote=TPR 7
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+120672_70518.0867.0RepeatNote=TPR 8
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+12080_11318.0867.0RepeatNote=TPR 2
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324124_129264.3333333333333365.0RegionLysophosphatidic acid binding
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035124_129264.3333333333333365.0RegionLysophosphatidic acid binding
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135124_129264.3333333333333365.0RegionLysophosphatidic acid binding
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324108_121264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324145_163264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324185_204264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST00000358883241_50264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324226_255264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST000003588832476_83264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035108_121264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035145_163264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035185_204264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST00000374430351_50264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035226_255264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST000003744303576_83264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135108_121264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135145_163264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135185_204264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST00000374431351_50264.3333333333333365.0Topological domainNote=Extracellular
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135226_255264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST000003744313576_83264.3333333333333365.0Topological domainNote=Cytoplasmic
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324122_144264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D3
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324164_184264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D4
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324205_225264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D5
TgeneLPAR1chr4:140222985chr9:113638002ENST0000035888324256_280264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D6
TgeneLPAR1chr4:140222985chr9:113638002ENST000003588832451_75264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D1
TgeneLPAR1chr4:140222985chr9:113638002ENST000003588832484_107264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D2
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035122_144264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D3
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035164_184264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D4
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035205_225264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D5
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443035256_280264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D6
TgeneLPAR1chr4:140222985chr9:113638002ENST000003744303551_75264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D1
TgeneLPAR1chr4:140222985chr9:113638002ENST000003744303584_107264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D2
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135122_144264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D3
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135164_184264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D4
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135205_225264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D5
TgeneLPAR1chr4:140222985chr9:113638002ENST0000037443135256_280264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D6
TgeneLPAR1chr4:140222985chr9:113638002ENST000003744313551_75264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D1
TgeneLPAR1chr4:140222985chr9:113638002ENST000003744313584_107264.3333333333333365.0TransmembraneNote=Helical%3B Name%3D2


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Fusion Protein Structures

check button PDB and CIF files of the predicted fusion proteins
* Here we show the 3D structure of the fusion proteins using Mol*. AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100. Model confidence is shown from the pLDDT values per residue. pLDDT corresponds to the model’s prediction of its score on the local Distance Difference Test. It is a measure of local accuracy (from AlphfaFold website). To color code individual residues, we transformed individual PDB files into CIF format.
Fusion protein PDB link (fusion AA seq ID in FusionPDB)HgeneHchrHbpHstrandTgeneTchrTbpTstrandAA seqLen(AA seq)
PDB file >>>77_NAA15_140222985_LPAR1_113638002_ranked_0.pdbNAA15140222985140222985ENST00000538760LPAR1chr9113638002-
MTEPGGGGSSGSSRNDAGREPPAQGECALQADLGAFIICWTPGLVLLLLDVCCPQCDVLAYEKFFLLLAEFNSAMNPIIYSYRDKEMSAT
133


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pLDDT score distribution

check button pLDDT score distribution of the predicted wild-type structures of two partner proteins from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
NAA15_pLDDT.png
all structure
all structure
LPAR1_pLDDT.png
all structure
all structure

check button pLDDT score distribution of the predicted fusion protein structures from AlphaFold2
* AlphaFold produces a per-residue confidence score (pLDDT) between 0 and 100.
all structure


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Ramachandran Plot of Fusion Protein Structure


check button Ramachandran plot of the torsional angles - phi (φ)and psi (ψ) - of the residues (amino acids) contained in this fusion protein peptide.
Fusion AA seq ID in FusionPDB and their Ramachandran plots

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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
NAA15
LPAR1


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
HgeneNAA15chr4:140222985chr9:113638002ENST00000296543+120500_86618.0867.0HYPK


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Related Drugs to NAA15-LPAR1


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 NAA15-LPAR1


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