Fusion Gene Studies
in Kim Lab

FusionBase FusionGDB FusionGDB2 FusionPDB FusionNeoAntigen FusionAI FusionNW FGviewer Publication Contact
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:FAM172A-FHIT (FusionGDB2 ID:HG83989TG2272)

Fusion Gene Summary for FAM172A-FHIT

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM172A-FHIT
Fusion gene ID: hg83989tg2272
HgeneTgene
Gene symbol

FAM172A

FHIT

Gene ID

83989

2272

Gene namefamily with sequence similarity 172 member Afragile histidine triad diadenosine triphosphatase
SynonymsC5orf21|ToupeeAP3Aase|FRA3B
Cytomap('FAM172A')('FHIT')

5q15

3p14.2

Type of geneprotein-codingprotein-coding
Descriptioncotranscriptional regulator FAM172Aprotein FAM172Abis(5'-adenosyl)-triphosphataseAP3A hydrolasediadenosine 5',5'''-P1,P3-triphosphate hydrolasedinucleosidetriphosphatase
Modification date2020031320200313
UniProtAcc.

P49789

Ensembl transtripts involved in fusion geneENST00000395965, ENST00000509163, 
ENST00000504768, ENST00000505869, 
ENST00000509739, 
Fusion gene scores* DoF score18 X 17 X 8=244827 X 20 X 11=5940
# samples 2332
** MAII scorelog2(23/2448*10)=-3.41189779174828
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(32/5940*10)=-4.21431912080077
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FAM172A [Title/Abstract] AND FHIT [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointFAM172A(93294482)-FHIT(59738047), # samples:3
Anticipated loss of major functional domain due to fusion event.FAM172A-FHIT 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.
FAM172A-FHIT 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.
FAM172A-FHIT seems lost the major protein functional domain in Hgene partner, which is a tumor suppressor due to the frame-shifted ORF.
FAM172A-FHIT seems lost the major protein functional domain in Tgene partner, which is a cell metabolism gene due to the frame-shifted ORF.
FAM172A-FHIT seems lost the major protein functional domain in Tgene partner, which is a CGC due to the frame-shifted ORF.
FAM172A-FHIT seems lost the major protein functional domain in Tgene partner, which is a tumor suppressor 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
TgeneFHIT

GO:0006163

purine nucleotide metabolic process

9323207


check buttonFusion gene breakpoints across FAM172A (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 FHIT (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check button Fusion gene information
* 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
ChimerDB4KIRCTCGA-B2-4101-01AFAM172Achr5

93294482

-FHITchr3

59738047

-


Top

Fusion Gene ORF analysis for FAM172A-FHIT

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-5UTRENST00000395965ENST00000341848FAM172Achr5

93294482

-FHITchr3

59738047

-
5CDS-5UTRENST00000395965ENST00000466788FAM172Achr5

93294482

-FHITchr3

59738047

-
5CDS-5UTRENST00000395965ENST00000468189FAM172Achr5

93294482

-FHITchr3

59738047

-
5CDS-5UTRENST00000509163ENST00000341848FAM172Achr5

93294482

-FHITchr3

59738047

-
5CDS-5UTRENST00000509163ENST00000466788FAM172Achr5

93294482

-FHITchr3

59738047

-
5CDS-5UTRENST00000509163ENST00000468189FAM172Achr5

93294482

-FHITchr3

59738047

-
5UTR-3CDSENST00000504768ENST00000476844FAM172Achr5

93294482

-FHITchr3

59738047

-
5UTR-3CDSENST00000504768ENST00000492590FAM172Achr5

93294482

-FHITchr3

59738047

-
5UTR-5UTRENST00000504768ENST00000341848FAM172Achr5

93294482

-FHITchr3

59738047

-
5UTR-5UTRENST00000504768ENST00000466788FAM172Achr5

93294482

-FHITchr3

59738047

-
5UTR-5UTRENST00000504768ENST00000468189FAM172Achr5

93294482

-FHITchr3

59738047

-
Frame-shiftENST00000509163ENST00000476844FAM172Achr5

93294482

-FHITchr3

59738047

-
Frame-shiftENST00000509163ENST00000492590FAM172Achr5

93294482

-FHITchr3

59738047

-
In-frameENST00000395965ENST00000476844FAM172Achr5

93294482

-FHITchr3

59738047

-
In-frameENST00000395965ENST00000492590FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-3CDSENST00000505869ENST00000476844FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-3CDSENST00000505869ENST00000492590FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-3CDSENST00000509739ENST00000476844FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-3CDSENST00000509739ENST00000492590FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-5UTRENST00000505869ENST00000341848FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-5UTRENST00000505869ENST00000466788FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-5UTRENST00000505869ENST00000468189FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-5UTRENST00000509739ENST00000341848FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-5UTRENST00000509739ENST00000466788FAM172Achr5

93294482

-FHITchr3

59738047

-
intron-5UTRENST00000509739ENST00000468189FAM172Achr5

93294482

-FHITchr3

59738047

-

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)
ENST00000395965FAM172Achr593294482-ENST00000476844FHITchr359738047-1070710140805221
ENST00000395965FAM172Achr593294482-ENST00000492590FHITchr359738047-1081710140805221

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
ENST00000395965ENST00000476844FAM172Achr593294482-FHITchr359738047-0.0033691950.99663085
ENST00000395965ENST00000492590FAM172Achr593294482-FHITchr359738047-0.003284970.99671507

Top

Fusion Genomic Features for FAM172A-FHIT


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.
genomic feature

Top

Fusion Protein Features for FAM172A-FHIT


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/chr5:93294482/chr3:59738047)
- 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
.FHIT

P49789

FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}.FUNCTION: Possesses dinucleoside triphosphate hydrolase activity (PubMed:12574506, PubMed:15182206, PubMed:8794732, PubMed:9323207, PubMed:9576908, PubMed:9543008). Cleaves P(1)-P(3)-bis(5'-adenosyl) triphosphate (Ap3A) to yield AMP and ADP (PubMed:12574506, PubMed:15182206, PubMed:8794732, PubMed:9323207, PubMed:9576908, PubMed:9543008). Can also hydrolyze P(1)-P(4)-bis(5'-adenosyl) tetraphosphate (Ap4A), but has extremely low activity with ATP (PubMed:8794732). Exhibits adenylylsulfatase activity, hydrolyzing adenosine 5'-phosphosulfate to yield AMP and sulfate (PubMed:18694747). Exhibits adenosine 5'-monophosphoramidase activity, hydrolyzing purine nucleotide phosphoramidates with a single phosphate group such as adenosine 5'monophosphoramidate (AMP-NH2) to yield AMP and NH2 (PubMed:18694747). Exhibits adenylylsulfate-ammonia adenylyltransferase, catalyzing the ammonolysis of adenosine 5'-phosphosulfate resulting in the formation of adenosine 5'-phosphoramidate (PubMed:26181368). Also catalyzes the ammonolysis of adenosine 5-phosphorofluoridate and diadenosine triphosphate (PubMed:26181368). Modulates transcriptional activation by CTNNB1 and thereby contributes to regulate the expression of genes essential for cell proliferation and survival, such as CCND1 and BIRC5 (PubMed:18077326). Plays a role in the induction of apoptosis via SRC and AKT1 signaling pathways (PubMed:16407838). Inhibits MDM2-mediated proteasomal degradation of p53/TP53 and thereby plays a role in p53/TP53-mediated apoptosis (PubMed:15313915). Induction of apoptosis depends on the ability of FHIT to bind P(1)-P(3)-bis(5'-adenosyl) triphosphate or related compounds, but does not require its catalytic activity, it may in part come from the mitochondrial form, which sensitizes the low-affinity Ca(2+) transporters, enhancing mitochondrial calcium uptake (PubMed:12574506, PubMed:19622739). Functions as tumor suppressor (By similarity). {ECO:0000250|UniProtKB:O89106, ECO:0000269|PubMed:12574506, ECO:0000269|PubMed:15313915, ECO:0000269|PubMed:16407838, ECO:0000269|PubMed:18077326, ECO:0000269|PubMed:18694747, ECO:0000269|PubMed:19622739, ECO:0000269|PubMed:26181368, ECO:0000269|PubMed:8794732, ECO:0000269|PubMed:9323207, ECO:0000269|PubMed:9543008}.

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
HgeneFAM172Achr5:93294482chr3:59738047ENST00000395965-611413_416189417.0MotifPrevents secretion from ER
HgeneFAM172Achr5:93294482chr3:59738047ENST00000505869-19413_4160307.0MotifPrevents secretion from ER
HgeneFAM172Achr5:93294482chr3:59738047ENST00000509163-510413_416143371.0MotifPrevents secretion from ER
TgeneFHITchr5:93294482chr3:59738047ENST00000341848352_109116148.0DomainHIT
TgeneFHITchr5:93294482chr3:59738047ENST00000468189792_109116148.0DomainHIT
TgeneFHITchr5:93294482chr3:59738047ENST000004768447102_109116214.0DomainHIT
TgeneFHITchr5:93294482chr3:59738047ENST000004925907102_109116205.33333333333334DomainHIT
TgeneFHITchr5:93294482chr3:59738047ENST000003418483594_98116148.0MotifHistidine triad motif
TgeneFHITchr5:93294482chr3:59738047ENST000004681897994_98116148.0MotifHistidine triad motif
TgeneFHITchr5:93294482chr3:59738047ENST0000047684471094_98116214.0MotifHistidine triad motif
TgeneFHITchr5:93294482chr3:59738047ENST0000049259071094_98116205.33333333333334MotifHistidine triad motif
TgeneFHITchr5:93294482chr3:59738047ENST000003418483589_92116148.0Nucleotide bindingSubstrate
TgeneFHITchr5:93294482chr3:59738047ENST000004681897989_92116148.0Nucleotide bindingSubstrate
TgeneFHITchr5:93294482chr3:59738047ENST0000047684471089_92116214.0Nucleotide bindingSubstrate
TgeneFHITchr5:93294482chr3:59738047ENST0000049259071089_92116205.33333333333334Nucleotide bindingSubstrate


Top

Fusion Gene Sequence for FAM172A-FHIT


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.
>28700_28700_1_FAM172A-FHIT_FAM172A_chr5_93294482_ENST00000395965_FHIT_chr3_59738047_ENST00000476844_length(transcript)=1070nt_BP=710nt
GGTCGGGGCGCGGATCCCGAGAGGGAAAGTCATAACAACCGCACGAGGGAGTTCGACTGGCGAACTGGAAGGCCACGCCTCCTCCCGCCT
GCCCCCTCAGCCCTGTGGCTGGGGGCAGAGCTCAGACTGTCTTCTGAAGATTGATGTCTATTTCCTTGAGCTCTTTAATTTTGTTGCCAA
TTTGGATAAACATGGCACAAATCCAGCAGGGAGGTCCAGATGAAAAAGAAAAGACTACCGCACTGAAAGATTTATTATCTAGGATAGATT
TGGATGAACTAATGAAAAAAGATGAACCGCCTCTTGATTTTCCTGATACCCTGGAAGGATTTGAATATGCTTTTAATGAAAAGGGACAGT
TAAGACACATAAAAACTGGGGAACCATTTGTTTTTAACTACCGGGAAGATTTACACAGATGGAACCAGAAAAGATACGAGGCTCTAGGAG
AGATCATCACGAAGTATGTATATGAGCTCCTGGAAAAGGATTGTAATTTGAAAAAAGTATCTATTCCAGTAGATGCCACTGAGAGTGAAC
CAAAGAGTTTTATCTTTATGAGTGAGGATGCTTTGACAAATCCACAGAAACTGATGGTTTTAATTCATGGTAGTGGTGTTGTCAGGGCAG
GGCAGTGGGCTAGAAGACTTATTATAAATGAAGATCTGGACAGTGGCACACAGATACCGTTTATTAAAAGAGCTGTGGCTCTCCAGAAAC
ATGACAAGGAGGACTTTCCTGCCTCTTGGAGATCAGAGGAGGAAATGGCAGCAGAAGCCGCAGCTCTGCGGGTCTACTTTCAGTGACACA
GATCCTGAATTCCAGCAAAAGAGCTATTGCCAACCAGTTTGAAGACCGCCCCCCGCCTCTCCCCAAGAGGAACTGAATCAGCATGAAAAT
GCAGTTTCTTCATCTCACCATCCTGTATTCTTCAACCAGTGATCCCCCACCTCGGTCACTCCAACTCCCTTAAAATACCTAGACCTAAAC

>28700_28700_1_FAM172A-FHIT_FAM172A_chr5_93294482_ENST00000395965_FHIT_chr3_59738047_ENST00000476844_length(amino acids)=221AA_BP=190
MMSISLSSLILLPIWINMAQIQQGGPDEKEKTTALKDLLSRIDLDELMKKDEPPLDFPDTLEGFEYAFNEKGQLRHIKTGEPFVFNYRED
LHRWNQKRYEALGEIITKYVYELLEKDCNLKKVSIPVDATESEPKSFIFMSEDALTNPQKLMVLIHGSGVVRAGQWARRLIINEDLDSGT

--------------------------------------------------------------
>28700_28700_2_FAM172A-FHIT_FAM172A_chr5_93294482_ENST00000395965_FHIT_chr3_59738047_ENST00000492590_length(transcript)=1081nt_BP=710nt
GGTCGGGGCGCGGATCCCGAGAGGGAAAGTCATAACAACCGCACGAGGGAGTTCGACTGGCGAACTGGAAGGCCACGCCTCCTCCCGCCT
GCCCCCTCAGCCCTGTGGCTGGGGGCAGAGCTCAGACTGTCTTCTGAAGATTGATGTCTATTTCCTTGAGCTCTTTAATTTTGTTGCCAA
TTTGGATAAACATGGCACAAATCCAGCAGGGAGGTCCAGATGAAAAAGAAAAGACTACCGCACTGAAAGATTTATTATCTAGGATAGATT
TGGATGAACTAATGAAAAAAGATGAACCGCCTCTTGATTTTCCTGATACCCTGGAAGGATTTGAATATGCTTTTAATGAAAAGGGACAGT
TAAGACACATAAAAACTGGGGAACCATTTGTTTTTAACTACCGGGAAGATTTACACAGATGGAACCAGAAAAGATACGAGGCTCTAGGAG
AGATCATCACGAAGTATGTATATGAGCTCCTGGAAAAGGATTGTAATTTGAAAAAAGTATCTATTCCAGTAGATGCCACTGAGAGTGAAC
CAAAGAGTTTTATCTTTATGAGTGAGGATGCTTTGACAAATCCACAGAAACTGATGGTTTTAATTCATGGTAGTGGTGTTGTCAGGGCAG
GGCAGTGGGCTAGAAGACTTATTATAAATGAAGATCTGGACAGTGGCACACAGATACCGTTTATTAAAAGAGCTGTGGCTCTCCAGAAAC
ATGACAAGGAGGACTTTCCTGCCTCTTGGAGATCAGAGGAGGAAATGGCAGCAGAAGCCGCAGCTCTGCGGGTCTACTTTCAGTGACACA
GATGTTTTTCAGATCCTGAATTCCAGCAAAAGAGCTATTGCCAACCAGTTTGAAGACCGCCCCCCGCCTCTCCCCAAGAGGAACTGAATC
AGCATGAAAATGCAGTTTCTTCATCTCACCATCCTGTATTCTTCAACCAGTGATCCCCCACCTCGGTCACTCCAACTCCCTTAAAATACC
TAGACCTAAACGGCTCAGACAGGCAGATTTGAGGTTTCCCCCTGTCTCCTTATTCGGCAGCCTTATGATTAAACTTCCTTCTCTGCTGCA

>28700_28700_2_FAM172A-FHIT_FAM172A_chr5_93294482_ENST00000395965_FHIT_chr3_59738047_ENST00000492590_length(amino acids)=221AA_BP=190
MMSISLSSLILLPIWINMAQIQQGGPDEKEKTTALKDLLSRIDLDELMKKDEPPLDFPDTLEGFEYAFNEKGQLRHIKTGEPFVFNYRED
LHRWNQKRYEALGEIITKYVYELLEKDCNLKKVSIPVDATESEPKSFIFMSEDALTNPQKLMVLIHGSGVVRAGQWARRLIINEDLDSGT

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

Top

Fusion Gene PPI Analysis for FAM172A-FHIT


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 FAM172A-FHIT


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 FAM172A-FHIT


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC0024121Lung Neoplasms2CTD_human
TgeneC0025500Mesothelioma2CTD_human
TgeneC0242379Malignant neoplasm of lung2CTD_human
TgeneC0007097Carcinoma1CTD_human
TgeneC0007131Non-Small Cell Lung Carcinoma1CTD_human
TgeneC0013146Drug abuse1CTD_human
TgeneC0013170Drug habituation1CTD_human
TgeneC0013222Drug Use Disorders1CTD_human
TgeneC0023903Liver neoplasms1CTD_human
TgeneC0024623Malignant neoplasm of stomach1CTD_human
TgeneC0029231Organic Mental Disorders, Substance-Induced1CTD_human
TgeneC0033578Prostatic Neoplasms1CTD_human
TgeneC0038356Stomach Neoplasms1CTD_human
TgeneC0038580Substance Dependence1CTD_human
TgeneC0038586Substance Use Disorders1CTD_human
TgeneC0042076Urologic Neoplasms1CTD_human
TgeneC0205696Anaplastic carcinoma1CTD_human
TgeneC0205697Carcinoma, Spindle-Cell1CTD_human
TgeneC0205698Undifferentiated carcinoma1CTD_human
TgeneC0205699Carcinomatosis1CTD_human
TgeneC0236733Amphetamine-Related Disorders1CTD_human
TgeneC0236804Amphetamine Addiction1CTD_human
TgeneC0236807Amphetamine Abuse1CTD_human
TgeneC0236969Substance-Related Disorders1CTD_human
TgeneC0345904Malignant neoplasm of liver1CTD_human
TgeneC0376358Malignant neoplasm of prostate1CTD_human
TgeneC0740858Substance abuse problem1CTD_human
TgeneC0751571Cancer of Urinary Tract1CTD_human
TgeneC1510472Drug Dependence1CTD_human
TgeneC1708349Hereditary Diffuse Gastric Cancer1CTD_human
TgeneC4316881Prescription Drug Abuse1CTD_human