FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact
Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:XPR1-NME7 (FusionGDB2 ID:99064)

Fusion Gene Summary for XPR1-NME7

check button Fusion gene summary
Fusion gene informationFusion gene name: XPR1-NME7
Fusion gene ID: 99064
HgeneTgene
Gene symbol

XPR1

NME7

Gene ID

9213

29922

Gene namexenotropic and polytropic retrovirus receptor 1NME/NM23 family member 7
SynonymsIBGC6|SLC53A1|SYG1|X3CFAP67|MN23H7|NDK 7|NDK7|nm23-H7
Cytomap

1q25.3

1q24.2

Type of geneprotein-codingprotein-coding
Descriptionxenotropic and polytropic retrovirus receptor 1X-receptorprotein SYG1 homologsolute carrier family 53 (phosphate exporter), member 1xenotropic and polytropic murine leukemia virus receptor X3nucleoside diphosphate kinase 7NDP kinase 7cilia and flagella associated protein 67non-metastatic cells 7, protein expressed in (nucleoside-diphosphate kinase)
Modification date2020031320200327
UniProtAcc.

Q9Y5B8

Ensembl transtripts involved in fusion geneENST00000367590, ENST00000367589, 
ENST00000467345, 		ENST00000472647, 
ENST00000367811, ENST00000469474, 
Fusion gene scores* DoF score24 X 7 X 12=201612 X 9 X 7=756
# samples 2713
** MAII scorelog2(27/2016*10)=-2.90046432644909
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0		log2(13/756*10)=-2.53987461119262
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: XPR1 [Title/Abstract] AND NME7 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointXPR1(180601406)-NME7(169138792), # samples:3
Anticipated loss of major functional domain due to fusion event.
* 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 buttonFusion gene breakpoints across XPR1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across NME7 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

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
ChimerDB4LIHCTCGA-G3-A25U-01AXPR1chr1

180601406

+NME7chr1

169138792

-
ChimerDB4LIHCTCGA-G3-A25U-01AXPR1chr1

180601406

+NME7chr1

169138792

-
ChimerDB4LIHCTCGA-G3-A25U-01AXPR1chr1

180601406

-NME7chr1

169138792

-


Top

Fusion Gene ORF analysis for XPR1-NME7

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-frameENST00000367590ENST00000472647XPR1chr1

180601406

+NME7chr1

169138792

-
In-frameENST00000367590ENST00000367811XPR1chr1

180601406

+NME7chr1

169138792

-
5CDS-intronENST00000367590ENST00000469474XPR1chr1

180601406

+NME7chr1

169138792

-
In-frameENST00000367589ENST00000472647XPR1chr1

180601406

+NME7chr1

169138792

-
In-frameENST00000367589ENST00000367811XPR1chr1

180601406

+NME7chr1

169138792

-
5CDS-intronENST00000367589ENST00000469474XPR1chr1

180601406

+NME7chr1

169138792

-
intron-3CDSENST00000467345ENST00000472647XPR1chr1

180601406

+NME7chr1

169138792

-
intron-3CDSENST00000467345ENST00000367811XPR1chr1

180601406

+NME7chr1

169138792

-
intron-intronENST00000467345ENST00000469474XPR1chr1

180601406

+NME7chr1

169138792

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)		BP loci
(transcript)		Predicted start
(transcript)		Predicted stop
(transcript)		Seq length
(amino acids)
ENST00000367590XPR1chr1180601406+ENST00000472647NME7chr1169138792-6622673012100
ENST00000367590XPR1chr1180601406+ENST00000367811NME7chr1169138792-6622673012100
ENST00000367589XPR1chr1180601406+ENST00000472647NME7chr1169138792-634239273191
ENST00000367589XPR1chr1180601406+ENST00000367811NME7chr1169138792-634239273191

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
ENST00000367590ENST00000472647XPR1chr1180601406+NME7chr1169138792-0.1134075150.88659245
ENST00000367590ENST00000367811XPR1chr1180601406+NME7chr1169138792-0.1134075150.88659245
ENST00000367589ENST00000472647XPR1chr1180601406+NME7chr1169138792-0.1171773150.88282275
ENST00000367589ENST00000367811XPR1chr1180601406+NME7chr1169138792-0.1171773150.88282275

Top

Fusion Genomic Features for XPR1-NME7


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

Top

Fusion Protein Features for XPR1-NME7


check button Go to

FGviewer for the breakpoints of chr1:180601406-chr1:169138792

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.NME7

Q9Y5B8

FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.FUNCTION: Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate.

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
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+1141_17723.0632.0DomainSPX
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114439_64323.0632.0DomainEXS
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+1151_17723.0697.0DomainSPX
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115439_64323.0697.0DomainEXS
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114158_16523.0632.0RegionImportant for inositol polyphosphate binding
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115158_16523.0697.0RegionImportant for inositol polyphosphate binding
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+1141_23623.0632.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114258_26423.0632.0Topological domainExtracellular
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114286_31823.0632.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114340_34523.0632.0Topological domainExtracellular
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114369_37623.0632.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114398_40223.0632.0Topological domainExtracellular
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114424_47323.0632.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114497_50723.0632.0Topological domainExtracellular
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114529_69623.0632.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+1151_23623.0697.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115258_26423.0697.0Topological domainExtracellular
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115286_31823.0697.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115340_34523.0697.0Topological domainExtracellular
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115369_37623.0697.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115398_40223.0697.0Topological domainExtracellular
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115424_47323.0697.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115497_50723.0697.0Topological domainExtracellular
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115529_69623.0697.0Topological domainCytoplasmic
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114237_25723.0632.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114265_28523.0632.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114319_33923.0632.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114346_36823.0632.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114377_39723.0632.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114403_42323.0632.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114474_49623.0632.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367589+114508_52823.0632.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115237_25723.0697.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115265_28523.0697.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115319_33923.0697.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115346_36823.0697.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115377_39723.0697.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115403_42323.0697.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115474_49623.0697.0TransmembraneHelical
HgeneXPR1chr1:180601406chr1:169138792ENST00000367590+115508_52823.0697.0TransmembraneHelical
TgeneNME7chr1:180601406chr1:169138792ENST000003678119123_91330.0377.0DomainDM10
TgeneNME7chr1:180601406chr1:169138792ENST000004726479123_91294.0341.0DomainDM10


Top

Fusion Gene Sequence for XPR1-NME7


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>In-frame_ENST00000367590_ENST00000472647_TCGA-G3-A25U-01A_XPR1_chr1_180601406_+_NME7_chr1_169138792_length(transcript)=662nt_BP=267nt
GCGGGGAGGGGCGGGGCTATGGAGAGGAGGAGGAAGATGGCGGGCGGGCTGCTCTGAAGAGACCTCGGCGGCGGCGGAGGAGGAGAGAAG
CGCAGCGCCGCGCCGCGCCGGGGCCCATGTGGGGAGGAGTCGGAGTCGCTGTTGCCGCCGCCGCCTGTAGCTGCTGGACCCGAGTGGGAG
TGAGGGGGAAACGGCAGGATGAAGTTCGCCGAGCACCTCTCCGCGCACATCACTCCCGAGTGGAGGAAGCAATACATCCAGTATGAGGAA
ATTGCCCGGCATTTACGCCCTGGAACTCTCAGAGCAATCTTTGGTAAAACTAAGATCCAGAATGCTGTTCACTGTACTGATCTGCCAGAG
GATGGCCTATTAGAGGTTCAATACTTCTTCAAGATCTTGGATAATTAGTGGTGTGGAAAGTAAAGAAGTCACAGGTTGGGACATTTAGAC
AAGAGTGAATCACACACGAGGAATGTGTTCATTCTTTTATTGTCCGTTGTTTTAACCTGACTGAATACAAGATCAACAAGAGCACTGTAC
TCCTGGCAATTATTACATATGTTAGAACATGGATTTTGCACTGTAGACAACATTTAACACCAGTCTATGGGGTACTGCATTGCTTTTTAT

>In-frame_ENST00000367590_ENST00000472647_TCGA-G3-A25U-01A_XPR1_chr1_180601406_+_NME7_chr1_169138792_length(amino acids)=100AA_start in transcript=301_stop in transcript=2
MRVPGRKCRAISSYWMYCFLHSGVMCAERCSANFILPFPPHSHSGPAATGGGGNSDSDSSPHGPRRGAALRFSPPPPPPRSLQSSPPAIF

--------------------------------------------------------------
>In-frame_ENST00000367590_ENST00000367811_TCGA-G3-A25U-01A_XPR1_chr1_180601406_+_NME7_chr1_169138792_length(transcript)=662nt_BP=267nt
GCGGGGAGGGGCGGGGCTATGGAGAGGAGGAGGAAGATGGCGGGCGGGCTGCTCTGAAGAGACCTCGGCGGCGGCGGAGGAGGAGAGAAG
CGCAGCGCCGCGCCGCGCCGGGGCCCATGTGGGGAGGAGTCGGAGTCGCTGTTGCCGCCGCCGCCTGTAGCTGCTGGACCCGAGTGGGAG
TGAGGGGGAAACGGCAGGATGAAGTTCGCCGAGCACCTCTCCGCGCACATCACTCCCGAGTGGAGGAAGCAATACATCCAGTATGAGGAA
ATTGCCCGGCATTTACGCCCTGGAACTCTCAGAGCAATCTTTGGTAAAACTAAGATCCAGAATGCTGTTCACTGTACTGATCTGCCAGAG
GATGGCCTATTAGAGGTTCAATACTTCTTCAAGATCTTGGATAATTAGTGGTGTGGAAAGTAAAGAAGTCACAGGTTGGGACATTTAGAC
AAGAGTGAATCACACACGAGGAATGTGTTCATTCTTTTATTGTCCGTTGTTTTAACCTGACTGAATACAAGATCAACAAGAGCACTGTAC
TCCTGGCAATTATTACATATGTTAGAACATGGATTTTGCACTGTAGACAACATTTAACACCAGTCTATGGGGTACTGCATTGCTTTTTAT

>In-frame_ENST00000367590_ENST00000367811_TCGA-G3-A25U-01A_XPR1_chr1_180601406_+_NME7_chr1_169138792_length(amino acids)=100AA_start in transcript=301_stop in transcript=2
MRVPGRKCRAISSYWMYCFLHSGVMCAERCSANFILPFPPHSHSGPAATGGGGNSDSDSSPHGPRRGAALRFSPPPPPPRSLQSSPPAIF

--------------------------------------------------------------
>In-frame_ENST00000367589_ENST00000472647_TCGA-G3-A25U-01A_XPR1_chr1_180601406_+_NME7_chr1_169138792_length(transcript)=634nt_BP=239nt
GGAGGAAGATGGCGGGCGGGCTGCTCTGAAGAGACCTCGGCGGCGGCGGAGGAGGAGAGAAGCGCAGCGCCGCGCCGCGCCGGGGCCCAT
GTGGGGAGGAGTCGGAGTCGCTGTTGCCGCCGCCGCCTGTAGCTGCTGGACCCGAGTGGGAGTGAGGGGGAAACGGCAGGATGAAGTTCG
CCGAGCACCTCTCCGCGCACATCACTCCCGAGTGGAGGAAGCAATACATCCAGTATGAGGAAATTGCCCGGCATTTACGCCCTGGAACTC
TCAGAGCAATCTTTGGTAAAACTAAGATCCAGAATGCTGTTCACTGTACTGATCTGCCAGAGGATGGCCTATTAGAGGTTCAATACTTCT
TCAAGATCTTGGATAATTAGTGGTGTGGAAAGTAAAGAAGTCACAGGTTGGGACATTTAGACAAGAGTGAATCACACACGAGGAATGTGT
TCATTCTTTTATTGTCCGTTGTTTTAACCTGACTGAATACAAGATCAACAAGAGCACTGTACTCCTGGCAATTATTACATATGTTAGAAC
ATGGATTTTGCACTGTAGACAACATTTAACACCAGTCTATGGGGTACTGCATTGCTTTTTATAAAGTTCAAAATAAAGATTTATTTTCAA

>In-frame_ENST00000367589_ENST00000472647_TCGA-G3-A25U-01A_XPR1_chr1_180601406_+_NME7_chr1_169138792_length(amino acids)=91AA_start in transcript=273_stop in transcript=1
MRVPGRKCRAISSYWMYCFLHSGVMCAERCSANFILPFPPHSHSGPAATGGGGNSDSDSSPHGPRRGAALRFSPPPPPPRSLQSSPPAIF

--------------------------------------------------------------
>In-frame_ENST00000367589_ENST00000367811_TCGA-G3-A25U-01A_XPR1_chr1_180601406_+_NME7_chr1_169138792_length(transcript)=634nt_BP=239nt
GGAGGAAGATGGCGGGCGGGCTGCTCTGAAGAGACCTCGGCGGCGGCGGAGGAGGAGAGAAGCGCAGCGCCGCGCCGCGCCGGGGCCCAT
GTGGGGAGGAGTCGGAGTCGCTGTTGCCGCCGCCGCCTGTAGCTGCTGGACCCGAGTGGGAGTGAGGGGGAAACGGCAGGATGAAGTTCG
CCGAGCACCTCTCCGCGCACATCACTCCCGAGTGGAGGAAGCAATACATCCAGTATGAGGAAATTGCCCGGCATTTACGCCCTGGAACTC
TCAGAGCAATCTTTGGTAAAACTAAGATCCAGAATGCTGTTCACTGTACTGATCTGCCAGAGGATGGCCTATTAGAGGTTCAATACTTCT
TCAAGATCTTGGATAATTAGTGGTGTGGAAAGTAAAGAAGTCACAGGTTGGGACATTTAGACAAGAGTGAATCACACACGAGGAATGTGT
TCATTCTTTTATTGTCCGTTGTTTTAACCTGACTGAATACAAGATCAACAAGAGCACTGTACTCCTGGCAATTATTACATATGTTAGAAC
ATGGATTTTGCACTGTAGACAACATTTAACACCAGTCTATGGGGTACTGCATTGCTTTTTATAAAGTTCAAAATAAAGATTTATTTTCAA

>In-frame_ENST00000367589_ENST00000367811_TCGA-G3-A25U-01A_XPR1_chr1_180601406_+_NME7_chr1_169138792_length(amino acids)=91AA_start in transcript=273_stop in transcript=1
MRVPGRKCRAISSYWMYCFLHSGVMCAERCSANFILPFPPHSHSGPAATGGGGNSDSDSSPHGPRRGAALRFSPPPPPPRSLQSSPPAIF

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

Top

Fusion Gene PPI Analysis for XPR1-NME7


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


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

Related Drugs for XPR1-NME7


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

Related Diseases for XPR1-NME7


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneXPR1C4225335BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 62CTD_human;GENOMICS_ENGLAND;UNIPROT
HgeneXPR1C0004782Basal Ganglia Diseases1CTD_human
HgeneXPR1C0006663Calcinosis1CTD_human
HgeneXPR1C0015371Extrapyramidal Disorders1CTD_human
HgeneXPR1C0015624Fanconi Syndrome1GENOMICS_ENGLAND
HgeneXPR1C0263628Tumoral calcinosis1CTD_human
HgeneXPR1C0393590Fahr's syndrome (disorder)1ORPHANET
HgeneXPR1C0521174Microcalcification1CTD_human
HgeneXPR1C0750951Lenticulostriate Disorders1CTD_human
TgeneNME7C0013146Drug abuse1CTD_human
TgeneNME7C0013170Drug habituation1CTD_human
TgeneNME7C0013222Drug Use Disorders1CTD_human
TgeneNME7C0029231Organic Mental Disorders, Substance-Induced1CTD_human
TgeneNME7C0037221Situs Inversus1ORPHANET
TgeneNME7C0038580Substance Dependence1CTD_human
TgeneNME7C0038586Substance Use Disorders1CTD_human
TgeneNME7C0236969Substance-Related Disorders1CTD_human
TgeneNME7C0238198Gastrointestinal Stromal Tumors1CTD_human
TgeneNME7C0740858Substance abuse problem1CTD_human
TgeneNME7C1510472Drug Dependence1CTD_human
TgeneNME7C3179349Gastrointestinal Stromal Sarcoma1CTD_human
TgeneNME7C4316881Prescription Drug Abuse1CTD_human