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Fusion Protein:LGR5-CNOT2 |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: LGR5-CNOT2 | FusionPDB ID: 44591 | FusionGDB2.0 ID: 44591 | Hgene | Tgene | Gene symbol | LGR5 | CNOT2 | Gene ID | 8549 | 4848 |
Gene name | leucine rich repeat containing G protein-coupled receptor 5 | CCR4-NOT transcription complex subunit 2 | |
Synonyms | FEX|GPR49|GPR67|GRP49|HG38 | CDC36|HSPC131|IDNADFS|NOT2|NOT2H | |
Cytomap | 12q21.1 | 12q15 | |
Type of gene | protein-coding | protein-coding | |
Description | leucine-rich repeat-containing G-protein coupled receptor 5G-protein coupled receptor 49G-protein coupled receptor 67G-protein coupled receptor HG38orphan G protein-coupled receptor HG38 | CCR4-NOT transcription complex subunit 2CCR4-associated factor 2negative regulator of transcription 2 | |
Modification date | 20200329 | 20200313 | |
UniProtAcc | O75473 | Q9NZN8 | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000266674, ENST00000536515, ENST00000540815, | ENST00000548230, ENST00000551483, ENST00000229195, ENST00000418359, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 5 X 3 X 2=30 | 27 X 20 X 10=5400 |
# samples | 5 | 29 | |
** MAII score | log2(5/30*10)=0.736965594166206 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | log2(29/5400*10)=-4.21883460192326 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: LGR5 [Title/Abstract] AND CNOT2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | LGR5(71928966)-CNOT2(70747609), # samples:2 | ||
Anticipated loss of major functional domain due to fusion event. | LGR5-CNOT2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. LGR5-CNOT2 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. LGR5-CNOT2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. LGR5-CNOT2 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. |
* 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 | LGR5 | GO:0090263 | positive regulation of canonical Wnt signaling pathway | 21693646|22815884 |
Tgene | CNOT2 | GO:0000122 | negative regulation of transcription by RNA polymerase II | 14707134|16712523 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
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![]() * 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 |
ChimerDB4 | BLCA | TCGA-ZF-AA4U-01A | LGR5 | chr12 | 71928966 | - | CNOT2 | chr12 | 70747609 | + |
ChimerDB4 | BLCA | TCGA-ZF-AA4U-01A | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747609 | + |
ChimerDB4 | BLCA | TCGA-ZF-AA4U | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747608 | + |
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Fusion ORF Analysis |
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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) |
ENST00000266674 | LGR5 | chr12 | 71928966 | + | ENST00000229195 | CNOT2 | chr12 | 70747608 | + | 1904 | 739 | 73 | 660 | 195 |
ENST00000266674 | LGR5 | chr12 | 71928966 | + | ENST00000418359 | CNOT2 | chr12 | 70747608 | + | 1904 | 739 | 73 | 660 | 195 |
ENST00000536515 | LGR5 | chr12 | 71928966 | + | ENST00000229195 | CNOT2 | chr12 | 70747608 | + | 1641 | 476 | 48 | 503 | 151 |
ENST00000536515 | LGR5 | chr12 | 71928966 | + | ENST00000418359 | CNOT2 | chr12 | 70747608 | + | 1641 | 476 | 48 | 503 | 151 |
ENST00000540815 | LGR5 | chr12 | 71928966 | + | ENST00000229195 | CNOT2 | chr12 | 70747608 | + | 1639 | 474 | 46 | 501 | 151 |
ENST00000540815 | LGR5 | chr12 | 71928966 | + | ENST00000418359 | CNOT2 | chr12 | 70747608 | + | 1639 | 474 | 46 | 501 | 151 |
ENST00000266674 | LGR5 | chr12 | 71928966 | + | ENST00000229195 | CNOT2 | chr12 | 70747609 | + | 1904 | 739 | 73 | 660 | 195 |
ENST00000266674 | LGR5 | chr12 | 71928966 | + | ENST00000418359 | CNOT2 | chr12 | 70747609 | + | 1904 | 739 | 73 | 660 | 195 |
ENST00000536515 | LGR5 | chr12 | 71928966 | + | ENST00000229195 | CNOT2 | chr12 | 70747609 | + | 1641 | 476 | 48 | 503 | 151 |
ENST00000536515 | LGR5 | chr12 | 71928966 | + | ENST00000418359 | CNOT2 | chr12 | 70747609 | + | 1641 | 476 | 48 | 503 | 151 |
ENST00000540815 | LGR5 | chr12 | 71928966 | + | ENST00000229195 | CNOT2 | chr12 | 70747609 | + | 1639 | 474 | 46 | 501 | 151 |
ENST00000540815 | LGR5 | chr12 | 71928966 | + | ENST00000418359 | CNOT2 | chr12 | 70747609 | + | 1639 | 474 | 46 | 501 | 151 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000266674 | ENST00000229195 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747608 | + | 0.03510942 | 0.96489054 |
ENST00000266674 | ENST00000418359 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747608 | + | 0.03510942 | 0.96489054 |
ENST00000536515 | ENST00000229195 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747608 | + | 0.023115512 | 0.97688454 |
ENST00000536515 | ENST00000418359 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747608 | + | 0.023115512 | 0.97688454 |
ENST00000540815 | ENST00000229195 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747608 | + | 0.019802682 | 0.9801973 |
ENST00000540815 | ENST00000418359 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747608 | + | 0.019802682 | 0.9801973 |
ENST00000266674 | ENST00000229195 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747609 | + | 0.03510942 | 0.96489054 |
ENST00000266674 | ENST00000418359 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747609 | + | 0.03510942 | 0.96489054 |
ENST00000536515 | ENST00000229195 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747609 | + | 0.023115512 | 0.97688454 |
ENST00000536515 | ENST00000418359 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747609 | + | 0.023115512 | 0.97688454 |
ENST00000540815 | ENST00000229195 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747609 | + | 0.019802682 | 0.9801973 |
ENST00000540815 | ENST00000418359 | LGR5 | chr12 | 71928966 | + | CNOT2 | chr12 | 70747609 | + | 0.019802682 | 0.9801973 |
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Fusion Amino Acid Sequences |
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>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >44591_44591_1_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000266674_CNOT2_chr12_70747608_ENST00000229195_length(amino acids)=195AA_BP= MSPLQPGLLRRPAWRQPAPLSPPRFSSPPTPWGQERGVWRCRRPLSCRSPRSGARRATARSSPVLLSARVRLVAPYFGHHGHLPARCAPV LACAAAAGDRGQLSQVWCVAEGLPHTLSLRARRQDVAQGGLLRPGALGAAFQPQRLHLLPRPQYEQHQSAAPESPAQSPLPGGVTSCGKR -------------------------------------------------------------- >44591_44591_2_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000266674_CNOT2_chr12_70747608_ENST00000418359_length(amino acids)=195AA_BP= MSPLQPGLLRRPAWRQPAPLSPPRFSSPPTPWGQERGVWRCRRPLSCRSPRSGARRATARSSPVLLSARVRLVAPYFGHHGHLPARCAPV LACAAAAGDRGQLSQVWCVAEGLPHTLSLRARRQDVAQGGLLRPGALGAAFQPQRLHLLPRPQYEQHQSAAPESPAQSPLPGGVTSCGKR -------------------------------------------------------------- >44591_44591_3_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000266674_CNOT2_chr12_70747609_ENST00000229195_length(amino acids)=195AA_BP= MSPLQPGLLRRPAWRQPAPLSPPRFSSPPTPWGQERGVWRCRRPLSCRSPRSGARRATARSSPVLLSARVRLVAPYFGHHGHLPARCAPV LACAAAAGDRGQLSQVWCVAEGLPHTLSLRARRQDVAQGGLLRPGALGAAFQPQRLHLLPRPQYEQHQSAAPESPAQSPLPGGVTSCGKR -------------------------------------------------------------- >44591_44591_4_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000266674_CNOT2_chr12_70747609_ENST00000418359_length(amino acids)=195AA_BP= MSPLQPGLLRRPAWRQPAPLSPPRFSSPPTPWGQERGVWRCRRPLSCRSPRSGARRATARSSPVLLSARVRLVAPYFGHHGHLPARCAPV LACAAAAGDRGQLSQVWCVAEGLPHTLSLRARRQDVAQGGLLRPGALGAAFQPQRLHLLPRPQYEQHQSAAPESPAQSPLPGGVTSCGKR -------------------------------------------------------------- >44591_44591_5_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000536515_CNOT2_chr12_70747608_ENST00000229195_length(amino acids)=151AA_BP= MDTSRLGVLLSLPVLLQLATGGSSPRSGVLLRGCPTHCHCEPDGRMLLRVDCSDLGLSELPSNLSVFTSYLDLSMNNISQLLPNPLPSLR -------------------------------------------------------------- >44591_44591_6_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000536515_CNOT2_chr12_70747608_ENST00000418359_length(amino acids)=151AA_BP= MDTSRLGVLLSLPVLLQLATGGSSPRSGVLLRGCPTHCHCEPDGRMLLRVDCSDLGLSELPSNLSVFTSYLDLSMNNISQLLPNPLPSLR -------------------------------------------------------------- >44591_44591_7_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000536515_CNOT2_chr12_70747609_ENST00000229195_length(amino acids)=151AA_BP= MDTSRLGVLLSLPVLLQLATGGSSPRSGVLLRGCPTHCHCEPDGRMLLRVDCSDLGLSELPSNLSVFTSYLDLSMNNISQLLPNPLPSLR -------------------------------------------------------------- >44591_44591_8_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000536515_CNOT2_chr12_70747609_ENST00000418359_length(amino acids)=151AA_BP= MDTSRLGVLLSLPVLLQLATGGSSPRSGVLLRGCPTHCHCEPDGRMLLRVDCSDLGLSELPSNLSVFTSYLDLSMNNISQLLPNPLPSLR -------------------------------------------------------------- >44591_44591_9_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000540815_CNOT2_chr12_70747608_ENST00000229195_length(amino acids)=151AA_BP= MDTSRLGVLLSLPVLLQLATGGSSPRSGVLLRGCPTHCHCEPDGRMLLRVDCSDLGLSELPSNLSVFTSYLDLSMNNISQLLPNPLPSLR -------------------------------------------------------------- >44591_44591_10_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000540815_CNOT2_chr12_70747608_ENST00000418359_length(amino acids)=151AA_BP= MDTSRLGVLLSLPVLLQLATGGSSPRSGVLLRGCPTHCHCEPDGRMLLRVDCSDLGLSELPSNLSVFTSYLDLSMNNISQLLPNPLPSLR -------------------------------------------------------------- >44591_44591_11_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000540815_CNOT2_chr12_70747609_ENST00000229195_length(amino acids)=151AA_BP= MDTSRLGVLLSLPVLLQLATGGSSPRSGVLLRGCPTHCHCEPDGRMLLRVDCSDLGLSELPSNLSVFTSYLDLSMNNISQLLPNPLPSLR -------------------------------------------------------------- >44591_44591_12_LGR5-CNOT2_LGR5_chr12_71928966_ENST00000540815_CNOT2_chr12_70747609_ENST00000418359_length(amino acids)=151AA_BP= MDTSRLGVLLSLPVLLQLATGGSSPRSGVLLRGCPTHCHCEPDGRMLLRVDCSDLGLSELPSNLSVFTSYLDLSMNNISQLLPNPLPSLR -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr12:71928966/chr12:70747609) - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. - How to search 1. Put your fusion gene symbol. 2. Press the tab key until there will be shown the breakpoint information filled. 4. Go down and press 'Search' tab twice. 4. Go down to have the hyperlink of the search result. 5. Click the hyperlink. 6. See the FGviewer result for your fusion gene. |
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Hgene | Tgene |
LGR5 | CNOT2 |
FUNCTION: Receptor for R-spondins that potentiates the canonical Wnt signaling pathway and acts as a stem cell marker of the intestinal epithelium and the hair follicle. Upon binding to R-spondins (RSPO1, RSPO2, RSPO3 or RSPO4), associates with phosphorylated LRP6 and frizzled receptors that are activated by extracellular Wnt receptors, triggering the canonical Wnt signaling pathway to increase expression of target genes. In contrast to classical G-protein coupled receptors, does not activate heterotrimeric G-proteins to transduce the signal. Involved in the development and/or maintenance of the adult intestinal stem cells during postembryonic development. {ECO:0000269|PubMed:21693646, ECO:0000269|PubMed:21727895, ECO:0000269|PubMed:21909076, ECO:0000269|PubMed:22815884, ECO:0000269|PubMed:23809763}. | FUNCTION: Component of the CCR4-NOT complex which is one of the major cellular mRNA deadenylases and is linked to various cellular processes including bulk mRNA degradation, miRNA-mediated repression, translational repression during translational initiation and general transcription regulation. Additional complex functions may be a consequence of its influence on mRNA expression. Required for the CCR4-NOT complex structural integrity. Can repress transcription and may link the CCR4-NOT complex to transcriptional regulation; the repressive function may specifically involve the N-Cor repressor complex containing HDAC3, NCOR1 and NCOR2. Involved in the maintenance of embryonic stem (ES) cell identity. {ECO:0000269|PubMed:14707134, ECO:0000269|PubMed:16712523, ECO:0000269|PubMed:21299754, ECO:0000269|PubMed:22367759}. |
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- 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 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 25_66 | 142.66666666666666 | 908.0 | Domain | Note=LRRNT |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 25_66 | 142.66666666666666 | 884.0 | Domain | Note=LRRNT |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 25_66 | 142.66666666666666 | 908.0 | Domain | Note=LRRNT |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 25_66 | 142.66666666666666 | 884.0 | Domain | Note=LRRNT |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 115_136 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 3 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 67_90 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 1 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 91_112 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 2 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 115_136 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 3 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 67_90 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 1 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 91_112 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 2 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 115_136 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 3 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 67_90 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 1 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 91_112 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 2 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 115_136 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 3 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 67_90 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 1 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 91_112 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 2 |
Tgene | CNOT2 | chr12:71928966 | chr12:70747608 | ENST00000551483 | 5 | 7 | 437_540 | 163.0 | 192.0 | Region | Note=Repressor domain | |
Tgene | CNOT2 | chr12:71928966 | chr12:70747609 | ENST00000551483 | 5 | 7 | 437_540 | 163.0 | 192.0 | Region | Note=Repressor domain |
- 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 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 139_160 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 4 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 163_184 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 5 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 187_208 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 6 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 211_232 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 7 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 235_256 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 8 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 258_279 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 9 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 282_303 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 10 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 306_328 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 11 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 329_350 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 12 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 353_374 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 13 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 375_396 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 14 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 399_420 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 15 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 423_446 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 16 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 139_160 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 4 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 163_184 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 5 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 187_208 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 6 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 211_232 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 7 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 235_256 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 8 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 258_279 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 9 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 282_303 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 10 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 306_328 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 11 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 329_350 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 12 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 353_374 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 13 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 375_396 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 14 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 399_420 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 15 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 423_446 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 16 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 139_160 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 4 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 163_184 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 5 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 187_208 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 6 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 211_232 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 7 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 235_256 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 8 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 258_279 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 9 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 282_303 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 10 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 306_328 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 11 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 329_350 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 12 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 353_374 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 13 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 375_396 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 14 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 399_420 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 15 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 423_446 | 142.66666666666666 | 908.0 | Repeat | Note=LRR 16 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 139_160 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 4 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 163_184 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 5 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 187_208 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 6 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 211_232 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 7 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 235_256 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 8 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 258_279 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 9 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 282_303 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 10 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 306_328 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 11 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 329_350 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 12 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 353_374 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 13 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 375_396 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 14 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 399_420 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 15 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 423_446 | 142.66666666666666 | 884.0 | Repeat | Note=LRR 16 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 22_561 | 142.66666666666666 | 908.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 583_593 | 142.66666666666666 | 908.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 615_638 | 142.66666666666666 | 908.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 660_682 | 142.66666666666666 | 908.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 704_722 | 142.66666666666666 | 908.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 744_767 | 142.66666666666666 | 908.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 789_802 | 142.66666666666666 | 908.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 824_907 | 142.66666666666666 | 908.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 22_561 | 142.66666666666666 | 884.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 583_593 | 142.66666666666666 | 884.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 615_638 | 142.66666666666666 | 884.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 660_682 | 142.66666666666666 | 884.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 704_722 | 142.66666666666666 | 884.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 744_767 | 142.66666666666666 | 884.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 789_802 | 142.66666666666666 | 884.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 824_907 | 142.66666666666666 | 884.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 22_561 | 142.66666666666666 | 908.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 583_593 | 142.66666666666666 | 908.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 615_638 | 142.66666666666666 | 908.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 660_682 | 142.66666666666666 | 908.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 704_722 | 142.66666666666666 | 908.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 744_767 | 142.66666666666666 | 908.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 789_802 | 142.66666666666666 | 908.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 824_907 | 142.66666666666666 | 908.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 22_561 | 142.66666666666666 | 884.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 583_593 | 142.66666666666666 | 884.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 615_638 | 142.66666666666666 | 884.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 660_682 | 142.66666666666666 | 884.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 704_722 | 142.66666666666666 | 884.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 744_767 | 142.66666666666666 | 884.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 789_802 | 142.66666666666666 | 884.0 | Topological domain | Extracellular |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 824_907 | 142.66666666666666 | 884.0 | Topological domain | Cytoplasmic |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 562_582 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D1 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 594_614 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D2 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 639_659 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D3 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 683_703 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D4 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 723_743 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D5 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 768_788 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D6 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000266674 | + | 4 | 18 | 803_823 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D7 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 562_582 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D1 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 594_614 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D2 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 639_659 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D3 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 683_703 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D4 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 723_743 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D5 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 768_788 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D6 |
Hgene | LGR5 | chr12:71928966 | chr12:70747608 | ENST00000540815 | + | 4 | 17 | 803_823 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D7 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 562_582 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D1 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 594_614 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D2 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 639_659 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D3 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 683_703 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D4 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 723_743 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D5 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 768_788 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D6 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000266674 | + | 4 | 18 | 803_823 | 142.66666666666666 | 908.0 | Transmembrane | Helical%3B Name%3D7 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 562_582 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D1 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 594_614 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D2 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 639_659 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D3 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 683_703 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D4 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 723_743 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D5 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 768_788 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D6 |
Hgene | LGR5 | chr12:71928966 | chr12:70747609 | ENST00000540815 | + | 4 | 17 | 803_823 | 142.66666666666666 | 884.0 | Transmembrane | Helical%3B Name%3D7 |
Tgene | CNOT2 | chr12:71928966 | chr12:70747608 | ENST00000229195 | 14 | 16 | 437_540 | 512.0 | 541.0 | Region | Note=Repressor domain | |
Tgene | CNOT2 | chr12:71928966 | chr12:70747608 | ENST00000418359 | 15 | 17 | 437_540 | 512.0 | 541.0 | Region | Note=Repressor domain | |
Tgene | CNOT2 | chr12:71928966 | chr12:70747609 | ENST00000229195 | 14 | 16 | 437_540 | 512.0 | 541.0 | Region | Note=Repressor domain | |
Tgene | CNOT2 | chr12:71928966 | chr12:70747609 | ENST00000418359 | 15 | 17 | 437_540 | 512.0 | 541.0 | Region | Note=Repressor domain |
Top |
Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
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Gene | STRING network |
LGR5 | ![]() |
CNOT2 |
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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 |
Top |
Related Drugs to LGR5-CNOT2 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
Top |
Related Diseases to LGR5-CNOT2 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | LGR5 | C0007102 | Malignant tumor of colon | 1 | CTD_human |
Hgene | LGR5 | C0009375 | Colonic Neoplasms | 1 | CTD_human |
Hgene | LGR5 | C0009402 | Colorectal Carcinoma | 1 | CTD_human |
Hgene | LGR5 | C0009404 | Colorectal Neoplasms | 1 | CTD_human |