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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: 35129

FusionGeneSummary for SNHG3_AIFM1

check button Fusion gene summary
Fusion gene informationFusion gene name: SNHG3_AIFM1
Fusion gene ID: 35129
HgeneTgene
Gene symbol

SNHG3

AIFM1

Gene ID

8420

9131

Gene namesmall nucleolar RNA host gene 3apoptosis inducing factor mitochondria associated 1
SynonymsNCRNA00014|RNU17C|RNU17D|U17HG|U17HG-A|U17HG-ABAIF|CMT2D|CMTX4|COWCK|COXPD6|DFNX5|NADMR|NAMSD|PDCD8
Cytomap

1p35.3

Xq26.1

Type of genencRNAprotein-coding
DescriptionU17 small nucleolar RNA hostsmall nucleolar RNA host gene (non-protein coding) 3small nucleolar RNA host gene 3 (non-protein coding)apoptosis-inducing factor 1, mitochondrialapoptosis-inducing factor, mitochondrion-associated, 1programmed cell death 8 (apoptosis-inducing factor)striatal apoptosis-inducing factortesticular secretory protein Li 4
Modification date2018051920180527
UniProtAcc

O95831

Ensembl transtripts involved in fusion geneENST00000364938, ENST00000460436, 
ENST00000440263, ENST00000535724, 
ENST00000346424, ENST00000319908, 
ENST00000287295, 
Fusion gene scores* DoF score15 X 7 X 4=4202 X 2 X 1=4
# samples 152
** MAII scorelog2(15/420*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(2/4*10)=2.32192809488736
Context

PubMed: SNHG3 [Title/Abstract] AND AIFM1 [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
TgeneAIFM1

GO:0006919

activation of cysteine-type endopeptidase activity involved in apoptotic process

17094969


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
ChiTaRS3.1BG108121SNHG3chr1

28835429

+AIFM1chrX

129265777

-
* 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-3CDSENST00000364938ENST00000460436SNHG3chr1

28835429

+AIFM1chrX

129265777

-
intron-3CDSENST00000364938ENST00000440263SNHG3chr1

28835429

+AIFM1chrX

129265777

-
intron-3UTRENST00000364938ENST00000535724SNHG3chr1

28835429

+AIFM1chrX

129265777

-
intron-3UTRENST00000364938ENST00000346424SNHG3chr1

28835429

+AIFM1chrX

129265777

-
intron-3UTRENST00000364938ENST00000319908SNHG3chr1

28835429

+AIFM1chrX

129265777

-
intron-3UTRENST00000364938ENST00000287295SNHG3chr1

28835429

+AIFM1chrX

129265777

-

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FusionProtFeatures for SNHG3_AIFM1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SNHG3

AIFM1

O95831

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}.

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 SNHG3_AIFM1


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 SNHG3_AIFM1


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


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RelatedDrugs for SNHG3_AIFM1


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

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RelatedDiseases for SNHG3_AIFM1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneAIFM1C0011853Diabetes Mellitus, Experimental1CTD_human
TgeneAIFM1C0011854Diabetes Mellitus, Insulin-Dependent1CTD_human
TgeneAIFM1C0020179Huntington Disease1CTD_human
TgeneAIFM1C0027540Necrosis1CTD_human
TgeneAIFM1C0035305Retinal Detachment1CTD_human
TgeneAIFM1C0795910COWCHOCK SYNDROME1ORPHANET;UNIPROT
TgeneAIFM1C1845095DEAFNESS, X-LINKED 5 (disorder)1ORPHANET;UNIPROT
TgeneAIFM1C3151753COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 61CTD_human;ORPHANET;UNIPROT
TgeneAIFM1C4277682Chemical and Drug Induced Liver Injury1CTD_human