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Fusion gene ID: 36179 |
FusionGeneSummary for SSR1_NTF3 |
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Fusion gene information | Fusion gene name: SSR1_NTF3 | Fusion gene ID: 36179 | Hgene | Tgene | Gene symbol | SSR1 | NTF3 | Gene ID | 6745 | 4908 |
Gene name | signal sequence receptor subunit 1 | neurotrophin 3 | |
Synonyms | TRAPA | HDNF|NGF-2|NGF2|NT-3|NT3 | |
Cytomap | 6p24.3 | 12p13.31 | |
Type of gene | protein-coding | protein-coding | |
Description | translocon-associated protein subunit alphaSSR alpha subunitSSR-alphaTRAP alphasignal sequence receptor subunit alphasignal sequence receptor, alphatranslocon-associated protein alpha subunit | neurotrophin-3nerve growth factor 2neurotrophic factor | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | P43307 | P20783 | |
Ensembl transtripts involved in fusion gene | ENST00000488834, ENST00000474597, ENST00000244763, ENST00000397511, ENST00000534851, ENST00000489567, ENST00000479365, ENST00000462112, | ENST00000535299, ENST00000423158, ENST00000331010, | |
Fusion gene scores | * DoF score | 10 X 11 X 4=440 | 1 X 1 X 1=1 |
# samples | 11 | 1 | |
** MAII score | log2(11/440*10)=-2 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(1/1*10)=3.32192809488736 | |
Context | PubMed: SSR1 [Title/Abstract] AND NTF3 [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 |
Tgene | NTF3 | GO:0000187 | activation of MAPK activity | 23027130 |
Tgene | NTF3 | GO:0002092 | positive regulation of receptor internalization | 23027130 |
Tgene | NTF3 | GO:0007169 | transmembrane receptor protein tyrosine kinase signaling pathway | 23027130 |
Tgene | NTF3 | GO:0008284 | positive regulation of cell proliferation | 23027130 |
Tgene | NTF3 | GO:0030335 | positive regulation of cell migration | 23027130 |
Tgene | NTF3 | GO:0032148 | activation of protein kinase B activity | 23027130 |
Tgene | NTF3 | GO:0033138 | positive regulation of peptidyl-serine phosphorylation | 23027130 |
Tgene | NTF3 | GO:0050731 | positive regulation of peptidyl-tyrosine phosphorylation | 23027130 |
Tgene | NTF3 | GO:0050732 | negative regulation of peptidyl-tyrosine phosphorylation | 23027130 |
Tgene | NTF3 | GO:0050930 | induction of positive chemotaxis | 23027130 |
Tgene | NTF3 | GO:0090630 | activation of GTPase activity | 23027130 |
Tgene | NTF3 | GO:2000251 | positive regulation of actin cytoskeleton reorganization | 23027130 |
![]() (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 | SARC | TCGA-PC-A5DN-01A | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
* 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-intron | ENST00000488834 | ENST00000535299 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000488834 | ENST00000423158 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-5UTR | ENST00000488834 | ENST00000331010 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
5CDS-intron | ENST00000474597 | ENST00000535299 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
5CDS-intron | ENST00000474597 | ENST00000423158 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
5CDS-5UTR | ENST00000474597 | ENST00000331010 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000244763 | ENST00000535299 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000244763 | ENST00000423158 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-5UTR | ENST00000244763 | ENST00000331010 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000397511 | ENST00000535299 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000397511 | ENST00000423158 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-5UTR | ENST00000397511 | ENST00000331010 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000534851 | ENST00000535299 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000534851 | ENST00000423158 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-5UTR | ENST00000534851 | ENST00000331010 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000489567 | ENST00000535299 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000489567 | ENST00000423158 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-5UTR | ENST00000489567 | ENST00000331010 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000479365 | ENST00000535299 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000479365 | ENST00000423158 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-5UTR | ENST00000479365 | ENST00000331010 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000462112 | ENST00000535299 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-intron | ENST00000462112 | ENST00000423158 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
intron-5UTR | ENST00000462112 | ENST00000331010 | SSR1 | chr6 | 7290101 | - | NTF3 | chr12 | 5603360 | + |
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FusionProtFeatures for SSR1_NTF3 |
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Hgene | Tgene |
SSR1 | NTF3 |
Seems to promote the survival of visceral andproprioceptive sensory neurons. |
![]() * 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 SSR1_NTF3 |
![]() (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 SSR1_NTF3 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
SSR1 | DKC1, UTP14A, EEF1A1, PTN, HSPA13, HDGF, ELAVL1, CUL3, CAND1, FBXO6, ACAD9, FLOT2, CCT2, ABCC2, SFXN1, ILF3, FKBP8, HNRNPM, TCP1, CCT5, ATP6V1C1, CCT4, SRSF1, PSAP, HM13, MDC1, SERPINA1, EDEM1, HSPA5, MYC, ODC1, SERPINF2, ILK, HUWE1, RPS6KB2, NTRK1, ATP5C1, CYC1, DDOST, PHB, ATAD3A, ATAD3B, ATP5L, ATP6V0D1, LMAN1, MAGT1, COX2, NDUFA9, NDUFB8, PHB2, RPN1, SSR3, TECR, TMX1, VDAC3, SSR4, UQCRC2, MED23, TCTN3, TMEM216, EZH2, SORT1, SEC61B, LTN1, ERBB3, ESRRB, DUSP23, ERGIC3, EDEM3 | NTF3 | NTRK1, NTRK2, NTRK3, MEOX2, LAMB1, PYGB, PYGL, ITIH3, MAD2L1BP |
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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 SSR1_NTF3 |
![]() (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 SSR1_NTF3 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | NTF3 | C0005586 | Bipolar Disorder | 2 | PSYGENET |
Tgene | NTF3 | C0027746 | Nerve Degeneration | 2 | CTD_human |
Tgene | NTF3 | C0004352 | Autistic Disorder | 1 | CTD_human |
Tgene | NTF3 | C0011882 | Diabetic Neuropathies | 1 | CTD_human |
Tgene | NTF3 | C0013080 | Down Syndrome | 1 | CTD_human |
Tgene | NTF3 | C0014549 | Tonic-Clonic Epilepsy | 1 | CTD_human |
Tgene | NTF3 | C0020429 | Hyperalgesia | 1 | CTD_human |
Tgene | NTF3 | C0036341 | Schizophrenia | 1 | CTD_human |
Tgene | NTF3 | C0038220 | Status Epilepticus | 1 | CTD_human |
Tgene | NTF3 | C0041696 | Unipolar Depression | 1 | PSYGENET |
Tgene | NTF3 | C0525045 | Mood Disorders | 1 | PSYGENET |
Tgene | NTF3 | C1269683 | Major Depressive Disorder | 1 | PSYGENET |
Tgene | NTF3 | C1384666 | hearing impairment | 1 | CTD_human |