FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 34010

FusionGeneSummary for SLAMF9_ALG12

check button Fusion gene summary
Fusion gene informationFusion gene name: SLAMF9_ALG12
Fusion gene ID: 34010
HgeneTgene
Gene symbol

SLAMF9

ALG12

Gene ID

89886

79087

Gene nameSLAM family member 9ALG12, alpha-1,6-mannosyltransferase
SynonymsCD2F-10|CD2F10|CD84-H1|CD84H1|SF2001CDG1G|ECM39|PP14673|hALG12
Cytomap

1q23.2

22q13.33

Type of geneprotein-codingprotein-coding
DescriptionSLAM family member 9CD2 family member 10CD84 homolog 1cluster of differentiation 2 antigen family member 10cluster of differentiation 84 homolog 1signaling lymphocytic activation molecule family member 2001signaling lymphocytic activation molecule fdol-P-Man:Man(7)GlcNAc(2)-PP-Dol alpha-1,6-mannosyltransferaseasparagine-linked glycosylation 12 homolog (S. cerevisiae, alpha-1,6-mannosyltransferase)asparagine-linked glycosylation 12 homolog (yeast, alpha-1,6-mannosyltransferase)asparagine-linked gl
Modification date2018032920180523
UniProtAcc

Q96A28

Q9BV10

Ensembl transtripts involved in fusion geneENST00000466773, ENST00000368092, 
ENST00000368093, 
ENST00000330817, 
Fusion gene scores* DoF score1 X 1 X 1=12 X 2 X 1=4
# samples 12
** MAII scorelog2(1/1*10)=3.32192809488736log2(2/4*10)=2.32192809488736
Context

PubMed: SLAMF9 [Title/Abstract] AND ALG12 [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
TgeneALG12

GO:0006488

dolichol-linked oligosaccharide biosynthetic process

11983712


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
ChiTaRS3.1AF311904SLAMF9chr1

159923932

-ALG12chr22

50312079

-
* 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
intron-5UTRENST00000466773ENST00000330817SLAMF9chr1

159923932

-ALG12chr22

50312079

-
intron-5UTRENST00000368092ENST00000330817SLAMF9chr1

159923932

-ALG12chr22

50312079

-
intron-5UTRENST00000368093ENST00000330817SLAMF9chr1

159923932

-ALG12chr22

50312079

-

Top

FusionProtFeatures for SLAMF9_ALG12


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SLAMF9

Q96A28

ALG12

Q9BV10

May play a role in the immune response.{ECO:0000269|PubMed:11300479}. Adds the eighth mannose residue in an alpha-1,6 linkageonto the dolichol-PP-oligosaccharide precursor (dolichol-PP-Man(7)GlcNAc(2)) required for protein glycosylation.

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


Top

FusionGeneSequence for SLAMF9_ALG12


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).

Top

FusionGenePPI for SLAMF9_ALG12


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

RelatedDrugs for SLAMF9_ALG12


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

Top

RelatedDiseases for SLAMF9_ALG12


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSLAMF9C0023893Liver Cirrhosis, Experimental1CTD_human
TgeneALG12C2931001Congenital disorder of glycosylation type 1G4CTD_human;ORPHANET;UNIPROT