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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: 1629

FusionGeneSummary for AMPD2_ALB

check button Fusion gene summary
Fusion gene informationFusion gene name: AMPD2_ALB
Fusion gene ID: 1629
HgeneTgene
Gene symbol

AMPD2

ALB

Gene ID

271

213

Gene nameadenosine monophosphate deaminase 2albumin
SynonymsPCH9|SPG63HSA|PRO0883|PRO0903|PRO1341
Cytomap

1p13.3

4q13.3

Type of geneprotein-codingprotein-coding
DescriptionAMP deaminase 2AMPDadenosine monophosphate deaminase 2 (isoform L)serum albumin
Modification date2018051920180522
UniProtAcc

Q01433

P02768

Ensembl transtripts involved in fusion geneENST00000526301, ENST00000342115, 
ENST00000528667, ENST00000256578, 
ENST00000358729, ENST00000528454, 
ENST00000393688, 		ENST00000295897, 
ENST00000415165, ENST00000503124, 
ENST00000509063, ENST00000401494, 
ENST00000505649, 
Fusion gene scores* DoF score2 X 2 X 2=827 X 26 X 2=1404
# samples 233
** MAII scorelog2(2/8*10)=1.32192809488736log2(33/1404*10)=-2.08900500605874
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: AMPD2 [Title/Abstract] AND ALB [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
TgeneALB

GO:0009267

cellular response to starvation

16245148

TgeneALB

GO:0019836

hemolysis by symbiont of host erythrocytes

16394536

TgeneALB

GO:0043066

negative regulation of apoptotic process

16153637

TgeneALB

GO:0051659

maintenance of mitochondrion location

16153637


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
TCGARVLIHCTCGA-DD-AAE2-01AAMPD2chr1

110171428

+ALBchr4

74270018

+
* 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
3UTR-5UTRENST00000526301ENST00000295897AMPD2chr1

110171428

+ALBchr4

74270018

+
3UTR-5UTRENST00000526301ENST00000415165AMPD2chr1

110171428

+ALBchr4

74270018

+
3UTR-5UTRENST00000526301ENST00000503124AMPD2chr1

110171428

+ALBchr4

74270018

+
3UTR-5UTRENST00000526301ENST00000509063AMPD2chr1

110171428

+ALBchr4

74270018

+
3UTR-5UTRENST00000526301ENST00000401494AMPD2chr1

110171428

+ALBchr4

74270018

+
3UTR-intronENST00000526301ENST00000505649AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000342115ENST00000295897AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000342115ENST00000415165AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000342115ENST00000503124AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000342115ENST00000509063AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000342115ENST00000401494AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-intronENST00000342115ENST00000505649AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528667ENST00000295897AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528667ENST00000415165AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528667ENST00000503124AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528667ENST00000509063AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528667ENST00000401494AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-intronENST00000528667ENST00000505649AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000256578ENST00000295897AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000256578ENST00000415165AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000256578ENST00000503124AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000256578ENST00000509063AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000256578ENST00000401494AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-intronENST00000256578ENST00000505649AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000358729ENST00000295897AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000358729ENST00000415165AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000358729ENST00000503124AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000358729ENST00000509063AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000358729ENST00000401494AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-intronENST00000358729ENST00000505649AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528454ENST00000295897AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528454ENST00000415165AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528454ENST00000503124AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528454ENST00000509063AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000528454ENST00000401494AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-intronENST00000528454ENST00000505649AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000393688ENST00000295897AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000393688ENST00000415165AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000393688ENST00000503124AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000393688ENST00000509063AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-5UTRENST00000393688ENST00000401494AMPD2chr1

110171428

+ALBchr4

74270018

+
5CDS-intronENST00000393688ENST00000505649AMPD2chr1

110171428

+ALBchr4

74270018

+

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FusionProtFeatures for AMPD2_ALB


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
AMPD2

Q01433

ALB

P02768


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 AMPD2_ALB


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 AMPD2_ALB


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
AMPD2NEDD4, TERF1, POT1, YWHAB, CSNK2B, INPPL1, SMEK1, PPP4R2, AMPD2, CCNDBP1, C14orf105, CTBP1, TBC1D9B, NTRK1, EPS8, CD44, GPBP1L1, DCAF8, SDC2, LZTS2, GPR156, SDC1, MLX, DDX17, NME7, TUBG1, TUBGCP4, TCHPALBLUC7L2, FCGRT, PRB3, AMBP, USP37, UIMC1, DMWD, PSMD4, NR5A2, YWHAG, PSMA3, TK1, IMMT, PFDN1, FBXO25, CRYAB, APP, EEF2K, ADRA1B, APOA1, APOC1, SETX, KCNMA1, PDE4B, CTSL, CDC45, GJC2, CDCP1, DDB1, FGA, FN1, GABBR1, HP, IGHG1, IGHG2, IGKV2-40, KRT10, KRT14, KRT9, KRT1, OR8D2, KLK3, ATM, OR2T6, TLN2, TTR, CACNA1I, ZNF232, PLAG1, RLF, AHSG, APOA4, APOC3, CRB1, EXOC6, SCAF1, GFAP, IGL, TSC22D1, IGKC, ITGB5, KRT6A, SERPING1, TTPAL, F2, AP1M1, AMPD3, APOA2, APOC2, CHKB, F7, C4A, CFB, CFD, CFH, CST3, DCD, ETF1, GSN, IGDCC4, HBA2, HPX, PHC3, ST13, DERL1, FAM71E2, QTRTD1, KIAA0232, ITIH1, KRT13, KRT16, KRT5, KRT6B, OBSL1, CTAGE5, AGA, NCOA3, OR3A2, PPBP, PF4V1, PCDH1, RANBP2, RYR2, SACS, SH3BP5, PLA2G4F, TIAM1, PRSS3, PRSS3P2, ZNF292, AP4E1, APOE, CABLES1, SLC25A13, NLRC4, CLCA2, DGKG, DMD, DICER1, GRAP2, TRAPPC11, SPATA31A7, PDZRN4, PALB2, LDB3, CEP44, ITGA2, JARID2, GCN1L1, CAMTA1, SLC9A8, CNOT1, LAT, MYL4, MYLK3, TTN, NPHS1, SLC1A5, PEG3, CROT, BBC3, RANBP3, SCN5A, SPAST, SLA2, THRAP3, SGOL2, PRSS1, DCC, SORBS3, IQCB1, PAN2, PARK2, FUS, CCDC8, LAMTOR5, CA8, GDPD1, PINX1, ZNF558, RPS6KB2, HNRNPA1, MED4, MED20, SOD1, LRP8, TIMM13, GAR1, FOXA3, FOXJ3, FOXP3, RC3H1, CDC73, CPS1, MAPK6, DDX31, SNX27, HSPA8, UPF3A, CCDC82, ADAMTS18, RALBP1, CYLD


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

RelatedDrugs for AMPD2_ALB


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneALBP02768DB00493CefotaximeSerum albuminsmall moleculeapproved
TgeneALBP02768DB01045RifampicinSerum albuminsmall moleculeapproved
TgeneALBP02768DB03255PhenolSerum albuminsmall moleculeapproved|experimental
TgeneALBP02768DB00276AmsacrineSerum albuminsmall moleculeapproved|investigational
TgeneALBP02768DB00545PyridostigmineSerum albuminsmall moleculeapproved|investigational
TgeneALBP02768DB06713NorelgestrominSerum albuminsmall moleculeapproved|investigational
TgeneALBP02768DB11638ArtenimolSerum albuminsmall moleculeapproved|investigational
TgeneALBP02768DB00199ErythromycinSerum albuminsmall moleculeapproved|investigational|vet_approved

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RelatedDiseases for AMPD2_ALB


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneAMPD2C4014354PONTOCEREBELLAR HYPOPLASIA, TYPE 91ORPHANET;UNIPROT
TgeneALBC0033687Proteinuria9CTD_human
TgeneALBC0017658Glomerulonephritis8CTD_human
TgeneALBC0022658Kidney Diseases8CTD_human
TgeneALBC0017665Membranous glomerulonephritis6CTD_human
TgeneALBC0027697Nephritis6CTD_human
TgeneALBC0027707Nephritis, Interstitial4CTD_human
TgeneALBC0038454Cerebrovascular accident4CTD_human
TgeneALBC0342185Hyperthyroxinemia, Familial Dysalbuminemic4CTD_human;UNIPROT
TgeneALBC0023893Liver Cirrhosis, Experimental3CTD_human
TgeneALBC0025290Aseptic Meningitis3CTD_human
TgeneALBC2609414Acute kidney injury3CTD_human
TgeneALBC0014544Epilepsy2CTD_human
TgeneALBC0020649Hypotension2CTD_human;HPO
TgeneALBC0023890Liver Cirrhosis2CTD_human
TgeneALBC0027726Nephrotic Syndrome2CTD_human
TgeneALBC0036830Serum Sickness2CTD_human
TgeneALBC0162557Liver Failure, Acute2CTD_human
TgeneALBC4277682Chemical and Drug Induced Liver Injury2CTD_human
TgeneALBC0002994Angioedema1CTD_human
TgeneALBC0003460Anuria1CTD_human
TgeneALBC0004509Azoospermia1CTD_human
TgeneALBC0006111Brain Diseases1CTD_human
TgeneALBC0007222Cardiovascular Diseases1CTD_human
TgeneALBC0007786Brain Ischemia1CTD_human
TgeneALBC0011581Depressive disorder1CTD_human
TgeneALBC0011875Diabetic Angiopathies1CTD_human
TgeneALBC0011881Diabetic Nephropathy1CTD_human
TgeneALBC0013502Echinococcosis1CTD_human
TgeneALBC0016059Fibrosis1CTD_human
TgeneALBC0017662Glomerulonephritis, Membranoproliferative1CTD_human
TgeneALBC0018799Heart Diseases1CTD_human
TgeneALBC0018801Heart failure1CTD_human
TgeneALBC0019061Hemolytic-Uremic Syndrome1CTD_human
TgeneALBC0019158Hepatitis1CTD_human
TgeneALBC0019693HIV Infections1CTD_human
TgeneALBC0019699HIV Seropositivity1CTD_human
TgeneALBC0020517Hypersensitivity1CTD_human
TgeneALBC0020522Delayed Hypersensitivity1CTD_human
TgeneALBC0020538Hypertensive disease1CTD_human
TgeneALBC0022548Keloid1CTD_human
TgeneALBC0022661Kidney Failure, Chronic1CTD_human
TgeneALBC0026848Myopathy1CTD_human
TgeneALBC0027055Myocardial Reperfusion Injury1CTD_human
TgeneALBC0027720Nephrosis1CTD_human
TgeneALBC0028797Occupational Diseases1CTD_human
TgeneALBC0030193Pain1CTD_human
TgeneALBC0030286Pancreatic Diseases1CTD_human
TgeneALBC0030305Pancreatitis1CTD_human
TgeneALBC0035222Respiratory Distress Syndrome, Adult1CTD_human
TgeneALBC0035242Respiratory Tract Diseases1CTD_human
TgeneALBC0035457Rhinitis, Allergic, Perennial1CTD_human
TgeneALBC0038325Stevens-Johnson Syndrome1CTD_human
TgeneALBC0038356Stomach Neoplasms1CTD_human
TgeneALBC0040034Thrombocytopenia1CTD_human
TgeneALBC0041755Adverse reaction to drug1CTD_human
TgeneALBC0042109Urticaria1CTD_human
TgeneALBC0042164Uveitis1CTD_human
TgeneALBC0152013Adenocarcinoma of lung (disorder)1CTD_human
TgeneALBC0239981Hypoalbuminemia1CTD_human;HPO
TgeneALBC0993582Arthritis, Experimental1CTD_human