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![]() | Fusion Gene Summary |
![]() | Fusion Gene ORF analysis |
![]() | Fusion Genomic Features |
![]() | Fusion Protein Features |
![]() | Fusion Gene Sequence |
![]() | Fusion Gene PPI analysis |
![]() | Related Drugs |
![]() | Related Diseases |
Fusion gene:SPPL3-LAMP2 (FusionGDB2 ID:85421) |
Fusion Gene Summary for SPPL3-LAMP2 |
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Fusion gene information | Fusion gene name: SPPL3-LAMP2 | Fusion gene ID: 85421 | Hgene | Tgene | Gene symbol | SPPL3 | LAMP2 | Gene ID | 121665 | 3920 |
Gene name | signal peptide peptidase like 3 | lysosomal associated membrane protein 2 | |
Synonyms | IMP2|MDHV1887|PRO4332|PSH1|PSL4 | CD107b|DND|LAMP-2|LAMPB|LGP-96|LGP110 | |
Cytomap | 12q24.31 | Xq24 | |
Type of gene | protein-coding | protein-coding | |
Description | signal peptide peptidase-like 3SPP-like 3intramembrane protease 2presenilin homologous protein 1presenilin-like protein 4 | lysosome-associated membrane glycoprotein 2CD107 antigen-like family member B | |
Modification date | 20200313 | 20200321 | |
UniProtAcc | . | P13473 | |
Ensembl transtripts involved in fusion gene | ENST00000353487, | ENST00000434600, ENST00000538785, ENST00000200639, ENST00000371335, ENST00000540603, | |
Fusion gene scores | * DoF score | 19 X 8 X 7=1064 | 10 X 10 X 1=100 |
# samples | 20 | 10 | |
** MAII score | log2(20/1064*10)=-2.41142624572647 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(10/100*10)=0 | |
Context | PubMed: SPPL3 [Title/Abstract] AND LAMP2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | SPPL3(121256004)-LAMP2(119582985), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. |
* 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 | SPPL3 | GO:0033619 | membrane protein proteolysis | 2313285 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
![]() * 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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChiTaRS5.0 | N/A | FN094428 | SPPL3 | chr12 | 121256004 | + | LAMP2 | chrX | 119582985 | - |
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Fusion Gene ORF analysis for SPPL3-LAMP2 |
![]() * 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 | ENST00000353487 | ENST00000434600 | SPPL3 | chr12 | 121256004 | + | LAMP2 | chrX | 119582985 | - |
intron-3CDS | ENST00000353487 | ENST00000538785 | SPPL3 | chr12 | 121256004 | + | LAMP2 | chrX | 119582985 | - |
intron-3CDS | ENST00000353487 | ENST00000200639 | SPPL3 | chr12 | 121256004 | + | LAMP2 | chrX | 119582985 | - |
intron-3CDS | ENST00000353487 | ENST00000371335 | SPPL3 | chr12 | 121256004 | + | LAMP2 | chrX | 119582985 | - |
intron-3CDS | ENST00000353487 | ENST00000540603 | SPPL3 | chr12 | 121256004 | + | LAMP2 | chrX | 119582985 | - |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for SPPL3-LAMP2 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
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Fusion Protein Features for SPPL3-LAMP2 |
![]() FGviewer for the breakpoints of :-: - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. |
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Hgene | Tgene |
. | LAMP2 |
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes. | FUNCTION: Plays an important role in chaperone-mediated autophagy, a process that mediates lysosomal degradation of proteins in response to various stresses and as part of the normal turnover of proteins with a long biological half-live (PubMed:8662539, PubMed:11082038, PubMed:18644871, PubMed:24880125, PubMed:27628032). Functions by binding target proteins, such as GAPDH and MLLT11, and targeting them for lysosomal degradation (PubMed:8662539, PubMed:11082038, PubMed:18644871, PubMed:24880125). Plays a role in lysosomal protein degradation in response to starvation (By similarity). Required for the fusion of autophagosomes with lysosomes during autophagy (PubMed:27628032). Cells that lack LAMP2 express normal levels of VAMP8, but fail to accumulate STX17 on autophagosomes, which is the most likely explanation for the lack of fusion between autophagosomes and lysosomes (PubMed:27628032). Required for normal degradation of the contents of autophagosomes (PubMed:27628032). Required for efficient MHCII-mediated presentation of exogenous antigens via its function in lysosomal protein degradation; antigenic peptides generated by proteases in the endosomal/lysosomal compartment are captured by nascent MHCII subunits (PubMed:20518820). Is not required for efficient MHCII-mediated presentation of endogenous antigens (PubMed:20518820). {ECO:0000250|UniProtKB:P17046, ECO:0000269|PubMed:11082038, ECO:0000269|PubMed:18644871, ECO:0000269|PubMed:20518820, ECO:0000269|PubMed:24880125, ECO:0000269|PubMed:27628032, ECO:0000269|PubMed:8662539}.; FUNCTION: [Isoform LAMP-2C]: Modulates chaperone-mediated autophagy. Decreases presentation of endogenous antigens by MHCII. Does not play a role in the presentation of exogenous and membrane-derived antigens by MHCII. {ECO:0000269|PubMed:26856698}. |
![]() * 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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Fusion Gene Sequence for SPPL3-LAMP2 |
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Fusion Gene PPI Analysis for SPPL3-LAMP2 |
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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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Related Drugs for SPPL3-LAMP2 |
![]() (DrugBank Version 5.1.8 2021-05-08) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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Related Diseases for SPPL3-LAMP2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | LAMP2 | C0878677 | Glycogen Storage Disease Type IIb | 15 | CLINGEN;CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Tgene | LAMP2 | C0038220 | Status Epilepticus | 1 | CTD_human |
Tgene | LAMP2 | C0270823 | Petit mal status | 1 | CTD_human |
Tgene | LAMP2 | C0311335 | Grand Mal Status Epilepticus | 1 | CTD_human |
Tgene | LAMP2 | C0393734 | Complex Partial Status Epilepticus | 1 | CTD_human |
Tgene | LAMP2 | C0751522 | Status Epilepticus, Subclinical | 1 | CTD_human |
Tgene | LAMP2 | C0751523 | Non-Convulsive Status Epilepticus | 1 | CTD_human |
Tgene | LAMP2 | C0751524 | Simple Partial Status Epilepticus | 1 | CTD_human |