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Fusion gene ID: 35251 |
FusionGeneSummary for SNX14_EYS |
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Fusion gene information | Fusion gene name: SNX14_EYS | Fusion gene ID: 35251 | Hgene | Tgene | Gene symbol | SNX14 | EYS | Gene ID | 57231 | 346007 |
Gene name | sorting nexin 14 | eyes shut homolog (Drosophila) | |
Synonyms | RGS-PX2|SCAR20 | C6orf178|C6orf179|C6orf180|EGFL10|EGFL11|RP25|SPAM|bA166P24.2|bA307F22.3|bA74E24.1|dJ1018A4.2|dJ22I17.2|dJ303F19.1 | |
Cytomap | 6q14.3 | 6q12 | |
Type of gene | protein-coding | protein-coding | |
Description | sorting nexin-14 | protein eyes shut homologEGF-like-domain, multiple 10EGF-like-domain, multiple 11epidermal growth factor-like protein 10epidermal growth factor-like protein 11protein spacemaker homolog | |
Modification date | 20180519 | 20180519 | |
UniProtAcc | Q9Y5W7 | Q5T1H1 | |
Ensembl transtripts involved in fusion gene | ENST00000346348, ENST00000314673, ENST00000513865, ENST00000505648, ENST00000508980, ENST00000369627, | ENST00000503581, ENST00000370621, ENST00000370616, ENST00000393380, ENST00000342421, ENST00000370618, ENST00000486069, | |
Fusion gene scores | * DoF score | 6 X 2 X 4=48 | 26 X 15 X 12=4680 |
# samples | 6 | 27 | |
** MAII score | log2(6/48*10)=0.321928094887362 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(27/4680*10)=-4.11547721741994 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: SNX14 [Title/Abstract] AND EYS [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 |
![]() (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 |
TCGA | RV | BRCA | TCGA-D8-A73W-01A | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
* 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 |
5CDS-5UTR | ENST00000346348 | ENST00000503581 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000346348 | ENST00000370621 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-intron | ENST00000346348 | ENST00000370616 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000346348 | ENST00000393380 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000346348 | ENST00000342421 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000346348 | ENST00000370618 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-intron | ENST00000346348 | ENST00000486069 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000314673 | ENST00000503581 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000314673 | ENST00000370621 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-intron | ENST00000314673 | ENST00000370616 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000314673 | ENST00000393380 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000314673 | ENST00000342421 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000314673 | ENST00000370618 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-intron | ENST00000314673 | ENST00000486069 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000513865 | ENST00000503581 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000513865 | ENST00000370621 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-intron | ENST00000513865 | ENST00000370616 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000513865 | ENST00000393380 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000513865 | ENST00000342421 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000513865 | ENST00000370618 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-intron | ENST00000513865 | ENST00000486069 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000505648 | ENST00000503581 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000505648 | ENST00000370621 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-intron | ENST00000505648 | ENST00000370616 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000505648 | ENST00000393380 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000505648 | ENST00000342421 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000505648 | ENST00000370618 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-intron | ENST00000505648 | ENST00000486069 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000508980 | ENST00000503581 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000508980 | ENST00000370621 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-intron | ENST00000508980 | ENST00000370616 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000508980 | ENST00000393380 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000508980 | ENST00000342421 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-5UTR | ENST00000508980 | ENST00000370618 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
intron-intron | ENST00000508980 | ENST00000486069 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000369627 | ENST00000503581 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000369627 | ENST00000370621 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-intron | ENST00000369627 | ENST00000370616 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000369627 | ENST00000393380 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000369627 | ENST00000342421 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-5UTR | ENST00000369627 | ENST00000370618 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
5CDS-intron | ENST00000369627 | ENST00000486069 | SNX14 | chr6 | 86303297 | - | EYS | chr6 | 66205886 | - |
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FusionProtFeatures for SNX14_EYS |
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Hgene | Tgene |
SNX14 | EYS |
Plays a role in maintaining normal neuronal excitabilityand synaptic transmission. May be involved in several stages ofintracellular trafficking (By similarity). Required forautophagosome clearance, possibly by mediating the fusion oflysosomes with autophagosomes (Probable). Bindsphosphatidylinositol 3,5-bisphosphate (PtdIns(3,5)P2), a keycomponent of late endosomes/lysosomes (PubMed:25848753). Does notbind phosphatidylinositol 3-phosphate (PtdIns(3P))(PubMed:25848753, PubMed:25148684). {ECO:0000250|UniProtKB:Q8BHY8,ECO:0000269|PubMed:25148684, ECO:0000269|PubMed:25848753,ECO:0000305|PubMed:25848753}. |
![]() * 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 SNX14_EYS |
![]() (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 SNX14_EYS |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
SNX14 | HNF1A, SHMT2, NXF1, TEX264, MCOLN3, IQCF1, CHRNA9, ATL3, TSPAN2, ZNRF4, CNGA3, IPPK, SLC4A8, SIGLECL1, PCDHGA5, TLR5, C3AR1, PMEL, FSHR, SLC17A2, PTGIR | EYS | EGFR |
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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 SNX14_EYS |
![]() (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 SNX14_EYS |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | SNX14 | C0007758 | Cerebellar Ataxia | 1 | CTD_human |
Hgene | SNX14 | C3714756 | Intellectual Disability | 1 | CTD_human |
Tgene | EYS | C1864446 | Retinitis Pigmentosa 25 | 2 | CTD_human;UNIPROT |
Tgene | EYS | C0035334 | Retinitis Pigmentosa | 1 | CTD_human;ORPHANET |