![]() |
||||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Fusion gene ID: 35129 |
FusionGeneSummary for SNHG3_AIFM1 |
![]() |
Fusion gene information | Fusion gene name: SNHG3_AIFM1 | Fusion gene ID: 35129 | Hgene | Tgene | Gene symbol | SNHG3 | AIFM1 | Gene ID | 8420 | 9131 |
Gene name | small nucleolar RNA host gene 3 | apoptosis inducing factor mitochondria associated 1 | |
Synonyms | NCRNA00014|RNU17C|RNU17D|U17HG|U17HG-A|U17HG-AB | AIF|CMT2D|CMTX4|COWCK|COXPD6|DFNX5|NADMR|NAMSD|PDCD8 | |
Cytomap | 1p35.3 | Xq26.1 | |
Type of gene | ncRNA | protein-coding | |
Description | U17 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 date | 20180519 | 20180527 | |
UniProtAcc | O95831 | ||
Ensembl transtripts involved in fusion gene | ENST00000364938, | ENST00000460436, ENST00000440263, ENST00000535724, ENST00000346424, ENST00000319908, ENST00000287295, | |
Fusion gene scores | * DoF score | 15 X 7 X 4=420 | 2 X 2 X 1=4 |
# samples | 15 | 2 | |
** MAII score | log2(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) |
![]() |
Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | AIFM1 | GO:0006919 | activation of cysteine-type endopeptidase activity involved in apoptotic process | 17094969 |
![]() (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 type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChiTaRS3.1 | BG108121 | SNHG3 | chr1 | 28835429 | + | AIFM1 | chrX | 129265777 | - |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
intron-3CDS | ENST00000364938 | ENST00000460436 | SNHG3 | chr1 | 28835429 | + | AIFM1 | chrX | 129265777 | - |
intron-3CDS | ENST00000364938 | ENST00000440263 | SNHG3 | chr1 | 28835429 | + | AIFM1 | chrX | 129265777 | - |
intron-3UTR | ENST00000364938 | ENST00000535724 | SNHG3 | chr1 | 28835429 | + | AIFM1 | chrX | 129265777 | - |
intron-3UTR | ENST00000364938 | ENST00000346424 | SNHG3 | chr1 | 28835429 | + | AIFM1 | chrX | 129265777 | - |
intron-3UTR | ENST00000364938 | ENST00000319908 | SNHG3 | chr1 | 28835429 | + | AIFM1 | chrX | 129265777 | - |
intron-3UTR | ENST00000364938 | ENST00000287295 | SNHG3 | chr1 | 28835429 | + | AIFM1 | chrX | 129265777 | - |
Top |
FusionProtFeatures for SNHG3_AIFM1 |
![]() |
Hgene | Tgene |
SNHG3 | AIFM1 |
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}. |
![]() * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Top |
FusionGeneSequence for SNHG3_AIFM1 |
![]() (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 SNHG3_AIFM1 |
![]() |
![]() |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Top |
RelatedDrugs for SNHG3_AIFM1 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Top |
RelatedDiseases for SNHG3_AIFM1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | AIFM1 | C0011853 | Diabetes Mellitus, Experimental | 1 | CTD_human |
Tgene | AIFM1 | C0011854 | Diabetes Mellitus, Insulin-Dependent | 1 | CTD_human |
Tgene | AIFM1 | C0020179 | Huntington Disease | 1 | CTD_human |
Tgene | AIFM1 | C0027540 | Necrosis | 1 | CTD_human |
Tgene | AIFM1 | C0035305 | Retinal Detachment | 1 | CTD_human |
Tgene | AIFM1 | C0795910 | COWCHOCK SYNDROME | 1 | ORPHANET;UNIPROT |
Tgene | AIFM1 | C1845095 | DEAFNESS, X-LINKED 5 (disorder) | 1 | ORPHANET;UNIPROT |
Tgene | AIFM1 | C3151753 | COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6 | 1 | CTD_human;ORPHANET;UNIPROT |
Tgene | AIFM1 | C4277682 | Chemical and Drug Induced Liver Injury | 1 | CTD_human |