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Fusion gene ID: 31102 |
FusionGeneSummary for RGS12_NSG1 |
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Fusion gene information | Fusion gene name: RGS12_NSG1 | Fusion gene ID: 31102 | Hgene | Tgene | Gene symbol | RGS12 | NSG1 | Gene ID | 6002 | 27065 |
Gene name | regulator of G protein signaling 12 | neuronal vesicle trafficking associated 1 | |
Synonyms | - | D4S234|D4S234E|NEEP21|P21 | |
Cytomap | 4p16.3 | 4p16.3 | |
Type of gene | protein-coding | protein-coding | |
Description | regulator of G-protein signaling 12regulator of G-protein signalling 12 | neuronal vesicle trafficking-associated protein 1brain neuron cytoplasmic protein 1carboxyterminally EE-tagged neuron-enriched endosomal 21 kDa proteinneuron specific gene family member 1neuron-enriched endosomal protein of 21 kDneuron-enriched endos | |
Modification date | 20180519 | 20180523 | |
UniProtAcc | O14924 | P42857 | |
Ensembl transtripts involved in fusion gene | ENST00000543385, ENST00000336727, ENST00000344733, ENST00000382788, ENST00000306648, ENST00000338806, ENST00000508158, ENST00000538395, | ENST00000421177, ENST00000513555, ENST00000450293, ENST00000505246, ENST00000506380, ENST00000397958, ENST00000433139, ENST00000504171, | |
Fusion gene scores | * DoF score | 6 X 6 X 4=144 | 1 X 1 X 1=1 |
# samples | 8 | 1 | |
** MAII score | log2(8/144*10)=-0.84799690655495 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(1/1*10)=3.32192809488736 | |
Context | PubMed: RGS12 [Title/Abstract] AND NSG1 [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 | LD | SKCM | TCGA-Z2-AA3V-06A | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
* 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 | ENST00000543385 | ENST00000421177 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
intron-3CDS | ENST00000543385 | ENST00000513555 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
intron-intron | ENST00000543385 | ENST00000450293 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
intron-intron | ENST00000543385 | ENST00000505246 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
intron-intron | ENST00000543385 | ENST00000506380 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
intron-intron | ENST00000543385 | ENST00000397958 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
intron-intron | ENST00000543385 | ENST00000433139 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
intron-intron | ENST00000543385 | ENST00000504171 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000336727 | ENST00000421177 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000336727 | ENST00000513555 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000336727 | ENST00000450293 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000336727 | ENST00000505246 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000336727 | ENST00000506380 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000336727 | ENST00000397958 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000336727 | ENST00000433139 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000336727 | ENST00000504171 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000344733 | ENST00000421177 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000344733 | ENST00000513555 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000344733 | ENST00000450293 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000344733 | ENST00000505246 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000344733 | ENST00000506380 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000344733 | ENST00000397958 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000344733 | ENST00000433139 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000344733 | ENST00000504171 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000382788 | ENST00000421177 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000382788 | ENST00000513555 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000382788 | ENST00000450293 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000382788 | ENST00000505246 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000382788 | ENST00000506380 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000382788 | ENST00000397958 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000382788 | ENST00000433139 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000382788 | ENST00000504171 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000306648 | ENST00000421177 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000306648 | ENST00000513555 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000306648 | ENST00000450293 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000306648 | ENST00000505246 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000306648 | ENST00000506380 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000306648 | ENST00000397958 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000306648 | ENST00000433139 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000306648 | ENST00000504171 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000338806 | ENST00000421177 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000338806 | ENST00000513555 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000338806 | ENST00000450293 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000338806 | ENST00000505246 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000338806 | ENST00000506380 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000338806 | ENST00000397958 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000338806 | ENST00000433139 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000338806 | ENST00000504171 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
3UTR-3CDS | ENST00000508158 | ENST00000421177 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
3UTR-3CDS | ENST00000508158 | ENST00000513555 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
3UTR-intron | ENST00000508158 | ENST00000450293 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
3UTR-intron | ENST00000508158 | ENST00000505246 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
3UTR-intron | ENST00000508158 | ENST00000506380 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
3UTR-intron | ENST00000508158 | ENST00000397958 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
3UTR-intron | ENST00000508158 | ENST00000433139 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
3UTR-intron | ENST00000508158 | ENST00000504171 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000538395 | ENST00000421177 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
Frame-shift | ENST00000538395 | ENST00000513555 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000538395 | ENST00000450293 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000538395 | ENST00000505246 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000538395 | ENST00000506380 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000538395 | ENST00000397958 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000538395 | ENST00000433139 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
5CDS-intron | ENST00000538395 | ENST00000504171 | RGS12 | chr4 | 3388164 | + | NSG1 | chr4 | 4411300 | + |
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FusionProtFeatures for RGS12_NSG1 |
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Hgene | Tgene |
RGS12 | NSG1 |
Plays a role in the recycling mechanism in neurons ofmultiple receptors, including AMPAR, APP and L1CAM and acts at thelevel of early endosomes to promote sorting of receptors toward arecycling pathway. Regulates sorting and recycling of GRIA2through interaction with GRIP1 and then contributes to theregulation of synaptic transmission and plasticity by affectingthe recycling and targeting of AMPA receptors to the synapse (Bysimilarity). Is required for faithful sorting of L1CAM to axons byfacilitating trafficking from somatodendritic early endosome orthe recycling endosome (By similarity). In an other hand, inducesapoptosis via the activation of CASP3 in response to DNA damage(PubMed:20599942, PubMed:20878061). {ECO:0000250|UniProtKB:P02683,ECO:0000250|UniProtKB:Q62092, ECO:0000269|PubMed:20599942,ECO:0000269|PubMed:20878061}. |
![]() * 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 RGS12_NSG1 |
![]() (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 RGS12_NSG1 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
RGS12 | GNAI1, GNAI3, GNAI2, CUL4A, EEF1A1, ARL4C, MTNR1A | NSG1 | SRPK1, SRPK2, BSCL2, CCDC155 |
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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 RGS12_NSG1 |
![]() (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 RGS12_NSG1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | RGS12 | C0036341 | Schizophrenia | 1 | CTD_human |