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Fusion gene ID: 17138 |
FusionGeneSummary for IGF1R_ADPGK |
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Fusion gene information | Fusion gene name: IGF1R_ADPGK | Fusion gene ID: 17138 | Hgene | Tgene | Gene symbol | IGF1R | ADPGK | Gene ID | 3480 | 83440 |
Gene name | insulin like growth factor 1 receptor | ADP dependent glucokinase | |
Synonyms | CD221|IGFIR|IGFR|JTK13 | 2610017G09Rik|ADP-GK | |
Cytomap | 15q26.3 | 15q24.1 | |
Type of gene | protein-coding | protein-coding | |
Description | insulin-like growth factor 1 receptorIGF-I receptorsoluble IGF1R variant 1soluble IGF1R variant 2 | ADP-dependent glucokinaseATP-dependent glucokinaserbBP-35 | |
Modification date | 20180527 | 20180519 | |
UniProtAcc | P08069 | Q9BRR6 | |
Ensembl transtripts involved in fusion gene | ENST00000268035, ENST00000558762, ENST00000560432, | ENST00000311669, ENST00000456471, ENST00000567733, | |
Fusion gene scores | * DoF score | 11 X 8 X 3=264 | 3 X 6 X 3=54 |
# samples | 11 | 8 | |
** MAII score | log2(11/264*10)=-1.26303440583379 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(8/54*10)=0.567040592723894 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: IGF1R [Title/Abstract] AND ADPGK [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 | IGF1R | GO:0043066 | negative regulation of apoptotic process | 12556535 |
Hgene | IGF1R | GO:0046328 | regulation of JNK cascade | 12556535 |
Hgene | IGF1R | GO:0046777 | protein autophosphorylation | 1846292|7679099|11162456 |
Hgene | IGF1R | GO:0048009 | insulin-like growth factor receptor signaling pathway | 7679099 |
Hgene | IGF1R | GO:0048015 | phosphatidylinositol-mediated signaling | 7692086 |
Hgene | IGF1R | GO:0051262 | protein tetramerization | 1846292 |
Hgene | IGF1R | GO:0051389 | inactivation of MAPKK activity | 12556535 |
Tgene | ADPGK | GO:0006006 | glucose metabolic process | 26555263 |
![]() (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-GM-A2DK-01A | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
* 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 |
Frame-shift | ENST00000268035 | ENST00000311669 | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
5CDS-intron | ENST00000268035 | ENST00000456471 | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
5CDS-intron | ENST00000268035 | ENST00000567733 | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
Frame-shift | ENST00000558762 | ENST00000311669 | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
5CDS-intron | ENST00000558762 | ENST00000456471 | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
5CDS-intron | ENST00000558762 | ENST00000567733 | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
intron-3CDS | ENST00000560432 | ENST00000311669 | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
intron-intron | ENST00000560432 | ENST00000456471 | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
intron-intron | ENST00000560432 | ENST00000567733 | IGF1R | chr15 | 99251336 | + | ADPGK | chr15 | 73064186 | - |
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FusionProtFeatures for IGF1R_ADPGK |
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Hgene | Tgene |
IGF1R | ADPGK |
Receptor tyrosine kinase which mediates actions ofinsulin-like growth factor 1 (IGF1). Binds IGF1 with high affinityand IGF2 and insulin (INS) with a lower affinity. The activatedIGF1R is involved in cell growth and survival control. IGF1R iscrucial for tumor transformation and survival of malignant cell.Ligand binding activates the receptor kinase, leading to receptorautophosphorylation, and tyrosines phosphorylation of multiplesubstrates, that function as signaling adapter proteins including,the insulin-receptor substrates (IRS1/2), Shc and 14-3-3 proteins.Phosphorylation of IRSs proteins lead to the activation of twomain signaling pathways: the PI3K-AKT/PKB pathway and the Ras-MAPKpathway. The result of activating the MAPK pathway is increasedcellular proliferation, whereas activating the PI3K pathwayinhibits apoptosis and stimulates protein synthesis.Phosphorylated IRS1 can activate the 85 kDa regulatory subunit ofPI3K (PIK3R1), leading to activation of several downstreamsubstrates, including protein AKT/PKB. AKT phosphorylation, inturn, enhances protein synthesis through mTOR activation andtriggers the antiapoptotic effects of IGFIR throughphosphorylation and inactivation of BAD. In parallel to PI3K-driven signaling, recruitment of Grb2/SOS by phosphorylated IRS1or Shc leads to recruitment of Ras and activation of the ras-MAPKpathway. In addition to these two main signaling pathways IGF1Rsignals also through the Janus kinase/signal transducer andactivator of transcription pathway (JAK/STAT). Phosphorylation ofJAK proteins can lead to phosphorylation/activation of signaltransducers and activators of transcription (STAT) proteins. Inparticular activation of STAT3, may be essential for thetransforming activity of IGF1R. The JAK/STAT pathway activatesgene transcription and may be responsible for the transformingactivity. JNK kinases can also be activated by the IGF1R. IGF1exerts inhibiting activities on JNK activation via phosphorylationand inhibition of MAP3K5/ASK1, which is able to directly associatewith the IGF1R. When present in a hybrid receptor with INSR, binds IGF1.PubMed:12138094 shows that hybrid receptors composed of IGF1R andINSR isoform Long are activated with a high affinity by IGF1, withlow affinity by IGF2 and not significantly activated by insulin,and that hybrid receptors composed of IGF1R and INSR isoform Shortare activated by IGF1, IGF2 and insulin. In contrast,PubMed:16831875 shows that hybrid receptors composed of IGF1R andINSR isoform Long and hybrid receptors composed of IGF1R and INSRisoform Short have similar binding characteristics, both bind IGF1and have a low affinity for insulin. | Catalyzes the phosphorylation of D-glucose to D-glucose6-phosphate using ADP as the phosphate donor. GDP and CDP canreplace ADP, but with reduced efficiency (By similarity).{ECO:0000250}. |
![]() * 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 IGF1R_ADPGK |
![]() (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 IGF1R_ADPGK |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
IGF1R | CSK, IRS1, YWHAE, SOCS1, YWHAG, GRB10, NEDD4, IGF1, EHD1, SNAP29, IGFBP3, ARHGEF12, JAK1, PIK3R3, SHC1, ESR1, EGFR, PTK2, PXN, PTPN11, YWHAB, VAV3, SOCS2, RASA1, GNAI1, SOCS3, PTPN1, GNB2L1, MDM2, CBL, EEA1, ERBB2, CAMP, ARRB2, TP53, ARRB1, APP, RUVBL1, HSP90AA1, SLC23A3, SH2B1, RPL11, AMY2A, FFAR2, GRB14, FBXO6, PHB2, KCNIP3, NTRK1, FDPS, BAP1, CYP17A1, HOXC6, IL13RA2, KLK5, LYPD3, MTA3, NAT2, THRSP, TRIM25, VPS45, PIK3R1, CRKL, STAT3, SYVN1, CHEK1, PRKDC, HDAC6, MTOR, CDKN2A, CDKN1B, PTPRR, PTPN6, PTPN7, PTPN12, PPM1A, PPM1F, MPZL2, SSH1, UNC5CL, LYZL2, SLAMF1, ILKAP, DUSP10, DUSP14, DUSP15, DUSP18, DUSP19, DUSP21, DUSP26, DUPD1, STYX, UBQLN1 | ADPGK | UBQLN4, ABCB8, STX7, STX12, HMOX2, DLK1, PLTP, TIMP3, GALNT7, UGT8, TOR1B, SLC39A12, MGAT1, EPHB4, EXTL2, PTPRN, MIPEP, CCPG1, KIAA1467, PDIA5, FAM213A, TMEM214, PXDN, GALNT4, C1GALT1C1, CSGALNACT2, TRIM25 |
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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 IGF1R_ADPGK |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | IGF1R | P08069 | DB00046 | Insulin Lispro | Insulin-like growth factor 1 receptor | biotech | approved |
Hgene | IGF1R | P08069 | DB00047 | Insulin Glargine | Insulin-like growth factor 1 receptor | biotech | approved |
Hgene | IGF1R | P08069 | DB00071 | Insulin Pork | Insulin-like growth factor 1 receptor | biotech | approved |
Hgene | IGF1R | P08069 | DB00030 | Insulin Human | Insulin-like growth factor 1 receptor | biotech | approved|investigational |
Hgene | IGF1R | P08069 | DB01277 | Mecasermin | Insulin-like growth factor 1 receptor | biotech | approved|investigational |
Hgene | IGF1R | P08069 | DB09098 | Somatrem | Insulin-like growth factor 1 receptor | biotech | approved|investigational|withdrawn |
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RelatedDiseases for IGF1R_ADPGK |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | IGF1R | C1849157 | Insulin-Like Growth Factor I, Resistance To | 3 | CTD_human;ORPHANET;UNIPROT |
Hgene | IGF1R | C0024115 | Lung diseases | 2 | CTD_human |
Hgene | IGF1R | C0235833 | Congenital diaphragmatic hernia | 2 | CTD_human |
Hgene | IGF1R | C2239176 | Liver carcinoma | 2 | CTD_human |
Hgene | IGF1R | C0002395 | Alzheimer's Disease | 1 | CTD_human |
Hgene | IGF1R | C0007621 | Neoplastic Cell Transformation | 1 | CTD_human |
Hgene | IGF1R | C0014170 | Endometrial Neoplasms | 1 | CTD_human |
Hgene | IGF1R | C0015934 | Fetal Growth Retardation | 1 | CTD_human;HPO |
Hgene | IGF1R | C0018273 | Growth Disorders | 1 | CTD_human |
Hgene | IGF1R | C0030567 | Parkinson Disease | 1 | CTD_human |
Hgene | IGF1R | C0031117 | Peripheral Neuropathy | 1 | CTD_human |
Hgene | IGF1R | C0035229 | Respiratory Insufficiency | 1 | CTD_human |
Hgene | IGF1R | C0037286 | Skin Neoplasms | 1 | CTD_human |
Hgene | IGF1R | C0206686 | Adrenocortical carcinoma | 1 | CTD_human |
Hgene | IGF1R | C0752347 | Lewy Body Disease | 1 | CTD_human |
Hgene | IGF1R | C1458155 | Mammary Neoplasms | 1 | CTD_human |
Hgene | IGF1R | C3495559 | Juvenile arthritis | 1 | CTD_human |