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Fusion gene ID: 35327 |
FusionGeneSummary for SNX6_ZC3H13 |
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Fusion gene information | Fusion gene name: SNX6_ZC3H13 | Fusion gene ID: 35327 | Hgene | Tgene | Gene symbol | SNX6 | ZC3H13 | Gene ID | 58533 | 23091 |
Gene name | sorting nexin 6 | zinc finger CCCH-type containing 13 | |
Synonyms | MSTP010|TFAF2 | KIAA0853|Xio | |
Cytomap | 14q13.1 | 13q14.13 | |
Type of gene | protein-coding | protein-coding | |
Description | sorting nexin-6TRAF4-associated factor 2tumor necrosis factor receptor-associated factor 4(TRAF4)-associated factor 2 | zinc finger CCCH domain-containing protein 13 | |
Modification date | 20180522 | 20180523 | |
UniProtAcc | Q9UNH7 | Q5T200 | |
Ensembl transtripts involved in fusion gene | ENST00000396526, ENST00000396534, ENST00000362031, ENST00000355110, | ENST00000242848, ENST00000378921, ENST00000282007, ENST00000470308, | |
Fusion gene scores | * DoF score | 6 X 6 X 4=144 | 6 X 7 X 3=126 |
# samples | 6 | 7 | |
** MAII score | log2(6/144*10)=-1.26303440583379 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(7/126*10)=-0.84799690655495 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: SNX6 [Title/Abstract] AND ZC3H13 [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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Hgene | SNX6 | GO:0030512 | negative regulation of transforming growth factor beta receptor signaling pathway | 11279102 |
Hgene | SNX6 | GO:0045892 | negative regulation of transcription, DNA-templated | 11279102|20830743 |
![]() (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 | BQ028676 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
* 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 | ENST00000396526 | ENST00000242848 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-intron | ENST00000396526 | ENST00000378921 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-intron | ENST00000396526 | ENST00000282007 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-5UTR | ENST00000396526 | ENST00000470308 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-3CDS | ENST00000396534 | ENST00000242848 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-intron | ENST00000396534 | ENST00000378921 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-intron | ENST00000396534 | ENST00000282007 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-5UTR | ENST00000396534 | ENST00000470308 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-3CDS | ENST00000362031 | ENST00000242848 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-intron | ENST00000362031 | ENST00000378921 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-intron | ENST00000362031 | ENST00000282007 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-5UTR | ENST00000362031 | ENST00000470308 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-3CDS | ENST00000355110 | ENST00000242848 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-intron | ENST00000355110 | ENST00000378921 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-intron | ENST00000355110 | ENST00000282007 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
intron-5UTR | ENST00000355110 | ENST00000470308 | SNX6 | chr14 | 35037953 | + | ZC3H13 | chr13 | 46577292 | + |
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FusionProtFeatures for SNX6_ZC3H13 |
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Hgene | Tgene |
SNX6 | ZC3H13 |
Involved in several stages of intracellular trafficking.Interacts with membranes phosphatidylinositol 3,4-bisphosphateand/or phosphatidylinositol 4,5-bisphosphate (Probable). Acts inpart as component of the retromer membrane-deforming SNX-BARsubcomplex (PubMed:19935774). The SNX-BAR retromer mediatesretrograde transport of cargo proteins from endosomes to thetrans-Golgi network (TGN) and is involved in endosome-to-plasmamembrane transport for cargo protein recycling. The SNX-BARsubcomplex functions to deform the donor membrane into a tubularprofile called endosome-to-TGN transport carrier (ETC) (Probable).Does not have in vitro vesicle-to-membrane remodeling activity(PubMed:23085988). Involved in retrograde endosome-to-TGNtransport of lysosomal enzyme receptor IGF2R (PubMed:17148574).May function as link between transport vesicles and dynactin(Probable). Negatively regulates retrograde transport of BACE1from the cell surface to the trans-Golgi network(PubMed:20354142). Involved in E-cadherin sorting and degradation;inhibits PIP5K1C isoform 3-mediated E-cadherin degradation(PubMed:24610942). In association with GIT1 involved in EGFRdegradation. Promotes lysosomal degradation of CDKN1B (Bysimilarity). May contribute to transcription regulation(Probable). {ECO:0000250|UniProtKB:Q6P8X1,ECO:0000269|PubMed:17148574, ECO:0000269|PubMed:19935774,ECO:0000269|PubMed:20354142, ECO:0000269|PubMed:23085988,ECO:0000269|PubMed:24610942, ECO:0000303|PubMed:19935774,ECO:0000303|PubMed:20830743, ECO:0000305}. | Associated component of the WMM complex, a complex thatmediates N6-methyladenosine (m6A) methylation of RNAs, amodification that plays a role in the efficiency of mRNA splicingand RNA processing (PubMed:29507755). Acts as a key regulator ofm6A methylation by promoting m6A methylation of mRNAs at the 3'-UTR (By similarity). Controls embryonic stem cells (ESCs)pluripotency via its role in m6A methylation (By similarity). Inthe WMM complex, anchors component of the MACOM subcomplex in thenucleus (By similarity). Also required for bridging WTAP to theRNA-binding component RBM15 (RBM15 or RBM15B) (By similarity).{ECO:0000250|UniProtKB:E9Q784}. |
![]() * 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 |
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FusionGeneSequence for SNX6_ZC3H13 |
![]() (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 SNX6_ZC3H13 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for SNX6_ZC3H13 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for SNX6_ZC3H13 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |