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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: 32753

FusionGeneSummary for SCAMP2_CHRNA9

check button Fusion gene summary
Fusion gene informationFusion gene name: SCAMP2_CHRNA9
Fusion gene ID: 32753
HgeneTgene
Gene symbol

SCAMP2

CHRNA9

Gene ID

10066

55584

Gene namesecretory carrier membrane protein 2cholinergic receptor nicotinic alpha 9 subunit
Synonyms-HSA243342|NACHRA9
Cytomap

15q24.1

4p14

Type of geneprotein-codingprotein-coding
Descriptionsecretory carrier-associated membrane protein 2testis secretory sperm-binding protein Li 219pneuronal acetylcholine receptor subunit alpha-9NACHR alpha 9acetylcholine receptor, neuronal nicotinic, alpha-9 subunitcholinergic receptor, nicotinic alpha 9cholinergic receptor, nicotinic, alpha 9 (neuronal)cholinergic receptor, nicotinic, alpha po
Modification date2018052320180523
UniProtAcc

O15127

Q9UGM1

Ensembl transtripts involved in fusion geneENST00000268099, ENST00000310169, 
ENST00000502377, 
Fusion gene scores* DoF score7 X 4 X 5=1403 X 1 X 3=9
# samples 83
** MAII scorelog2(8/140*10)=-0.807354922057604
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/9*10)=1.73696559416621
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SCAMP2 [Title/Abstract] AND CHRNA9 [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
HgeneSCAMP2

GO:0015031

protein transport

15840657


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
TCGALDSARCTCGA-QQ-A5VA-01ASCAMP2chr15

75137814

-CHRNA9chr4

40350899

+
* 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
Frame-shiftENST00000268099ENST00000310169SCAMP2chr15

75137814

-CHRNA9chr4

40350899

+
5CDS-intronENST00000268099ENST00000502377SCAMP2chr15

75137814

-CHRNA9chr4

40350899

+

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FusionProtFeatures for SCAMP2_CHRNA9


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SCAMP2

O15127

CHRNA9

Q9UGM1

Functions in post-Golgi recycling pathways. Acts as arecycling carrier to the cell surface. Ionotropic receptor with a probable role in themodulation of auditory stimuli. Agonist binding induces aconformation change that leads to the opening of an ion-conductingchannel across the plasma membrane (PubMed:11752216,PubMed:25282151). The channel is permeable to a range of divalentcations including calcium, the influx of which may activate apotassium current which hyperpolarizes the cell membrane(PubMed:11752216, PubMed:25282151). In the ear, this may lead to areduction in basilar membrane motion, altering the activity ofauditory nerve fibers and reducing the range of dynamic hearing.This may protect against acoustic trauma. May also regulatekeratinocyte adhesion (PubMed:11021840).{ECO:0000269|PubMed:11021840, ECO:0000269|PubMed:11752216,ECO:0000269|PubMed:25282151, ECO:0000305}.

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 SCAMP2_CHRNA9


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 SCAMP2_CHRNA9


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
SCAMP2ST3GAL3, ARIH2, SNAP23, SCAMP1, ATP4A, TSPAN5, GPM6A, ASGR2, DLK1, ART3, RTN4, BSCL2, LPAR1, BCAP31, JAGN1, PHB, RPN1, ATP5L, TCTN3, TMEM17, REEP5, NCAPHCHRNA9POM121, KIAA0922, FAM76B, NUFIP2, SLC30A1, SPECC1L, SLC12A9, TMX2, METTL9, NETO2, KIF5B, KIF5A, C1orf43, CCPG1, POMGNT2, CKAP4, TMEM39B, KLC2, KLC4, DHRS7, SLC30A5, LRRC59, C3orf58, PBXIP1, CISD2, CELSR1, LEMD2, KIAA1715, GOLM1, DROSHA, GHDC, BTN2A2, HS2ST1, EPHX1, HMOX1, GRAMD1A, ATF6B, HMGCR, TMUB1, PPP1R15B, TMEM57, CHEK1, SLC30A6, ATP11C, HS6ST1, FUT8, ZDHHC9, PDE3B, TMEM39A, SNX14, SLC30A7, PDZD8, DNAJC18, ERGIC2, RER1, YKT6, MAVS, FAM189B, C19orf52, DDRGK1, EIF2AK3, ST7, TMEM120B, MAP7, DNAJC30, LCLAT1, ZNF785, C9orf91, ANKRD10, POLR3GL, NUS1, PCDHGC3


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 SCAMP2_CHRNA9


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneCHRNA9Q9UGM1DB00184NicotineNeuronal acetylcholine receptor subunit alpha-9small moleculeapproved
TgeneCHRNA9Q9UGM1DB00674GalantamineNeuronal acetylcholine receptor subunit alpha-9small moleculeapproved
TgeneCHRNA9Q9UGM1DB00898EthanolNeuronal acetylcholine receptor subunit alpha-9small moleculeapproved

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RelatedDiseases for SCAMP2_CHRNA9


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource