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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:CTIF-DYM (FusionGDB2 ID:HG9811TG54808) |
Fusion Gene Summary for CTIF-DYM |
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Fusion gene information | Fusion gene name: CTIF-DYM | Fusion gene ID: hg9811tg54808 | Hgene | Tgene | Gene symbol | CTIF | DYM | Gene ID | 9811 | 54808 |
Gene name | cap binding complex dependent translation initiation factor | dymeclin | |
Synonyms | Gm672|KIAA0427 | DMC|SMC | |
Cytomap | ('CTIF')('DYM') 18q21.1 | 18q21.1 | |
Type of gene | protein-coding | protein-coding | |
Description | CBP80/20-dependent translation initiation factor | dymeclindyggve-Melchior-Clausen syndrome protein | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | . | Q7RTS9 | |
Ensembl transtripts involved in fusion gene | ENST00000256413, ENST00000382998, ENST00000592658, | ENST00000592658, ENST00000256413, ENST00000382998, | |
Fusion gene scores | * DoF score | 20 X 11 X 10=2200 | 19 X 11 X 13=2717 |
# samples | 23 | 24 | |
** MAII score | log2(23/2200*10)=-3.25779775746765 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(24/2717*10)=-3.50090825461346 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: CTIF [Title/Abstract] AND DYM [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | CTIF(46197115)-DYM(46645296), # samples:1 | ||
Anticipated loss of major functional domain due to fusion event. | CTIF-DYM 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. CTIF-DYM 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. DYM-CTIF seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted 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 |
![]() * 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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![]() * 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 | BRCA | TCGA-D8-A141-01A | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
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Fusion Gene ORF analysis for CTIF-DYM |
![]() * 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 |
5CDS-intron | ENST00000256413 | ENST00000578396 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
5CDS-intron | ENST00000256413 | ENST00000584977 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
5CDS-intron | ENST00000382998 | ENST00000578396 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
5CDS-intron | ENST00000382998 | ENST00000584977 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
In-frame | ENST00000256413 | ENST00000269445 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
In-frame | ENST00000256413 | ENST00000442713 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
In-frame | ENST00000382998 | ENST00000269445 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
In-frame | ENST00000382998 | ENST00000442713 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
intron-3CDS | ENST00000592658 | ENST00000269445 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
intron-3CDS | ENST00000592658 | ENST00000442713 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
intron-intron | ENST00000592658 | ENST00000578396 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
intron-intron | ENST00000592658 | ENST00000584977 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - |
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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) |
ENST00000256413 | CTIF | chr18 | 46197115 | + | ENST00000442713 | DYM | chr18 | 46645296 | - | 1635 | 802 | 295 | 1248 | 317 |
ENST00000256413 | CTIF | chr18 | 46197115 | + | ENST00000269445 | DYM | chr18 | 46645296 | - | 1484 | 802 | 295 | 1248 | 317 |
ENST00000382998 | CTIF | chr18 | 46197115 | + | ENST00000442713 | DYM | chr18 | 46645296 | - | 1597 | 764 | 257 | 1210 | 317 |
ENST00000382998 | CTIF | chr18 | 46197115 | + | ENST00000269445 | DYM | chr18 | 46645296 | - | 1446 | 764 | 257 | 1210 | 317 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000256413 | ENST00000442713 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - | 0.004427724 | 0.9955722 |
ENST00000256413 | ENST00000269445 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - | 0.005141721 | 0.99485826 |
ENST00000382998 | ENST00000442713 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - | 0.004614936 | 0.9953851 |
ENST00000382998 | ENST00000269445 | CTIF | chr18 | 46197115 | + | DYM | chr18 | 46645296 | - | 0.005854943 | 0.9941451 |
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Fusion Genomic Features for CTIF-DYM |
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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 CTIF-DYM |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr18:46197115/chr18:46645296) - 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 |
. | DYM |
FUNCTION: Transcriptional activator which is required for calcium-dependent dendritic growth and branching in cortical neurons. Recruits CREB-binding protein (CREBBP) to nuclear bodies. Component of the CREST-BRG1 complex, a multiprotein complex that regulates promoter activation by orchestrating a calcium-dependent release of a repressor complex and a recruitment of an activator complex. In resting neurons, transcription of the c-FOS promoter is inhibited by BRG1-dependent recruitment of a phospho-RB1-HDAC1 repressor complex. Upon calcium influx, RB1 is dephosphorylated by calcineurin, which leads to release of the repressor complex. At the same time, there is increased recruitment of CREBBP to the promoter by a CREST-dependent mechanism, which leads to transcriptional activation. The CREST-BRG1 complex also binds to the NR2B promoter, and activity-dependent induction of NR2B expression involves a release of HDAC1 and recruitment of CREBBP (By similarity). {ECO:0000250}. | FUNCTION: Necessary for correct organization of Golgi apparatus. Involved in bone development. {ECO:0000269|PubMed:21280149}. |
![]() * 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 |
Hgene | CTIF | chr18:46197115 | chr18:46645296 | ENST00000256413 | + | 6 | 12 | 376_577 | 169 | 599.0 | Domain | Note=MIF4G |
Hgene | CTIF | chr18:46197115 | chr18:46645296 | ENST00000382998 | + | 7 | 13 | 376_577 | 169 | 601.0 | Domain | Note=MIF4G |
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Fusion Gene Sequence for CTIF-DYM |
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>20234_20234_1_CTIF-DYM_CTIF_chr18_46197115_ENST00000256413_DYM_chr18_46645296_ENST00000269445_length(transcript)=1484nt_BP=802nt CTTTCCCTGTGTCAGATCAGGGATCATTTTTTTTCCTTCCTCTACTCCCTCCCCCCTACCCGCCCCTCCCTCCCTGTTTCCCTTCCCTCC CTCCCTCCCCTCTCTGCTGGGTCTGTGCGCTGGGGCGCCCGATCCCCTCCGCAGCTGGGACGCTCCGAACTCGAGGCAGGAGTCGGCTCT CCGGAGCCTCGTCCCTCCCTTCCCCTTCCCTGCCCCCTTCCCCCACCCCCGACTCGGGCTTGGCGCGGCGGCCAGAGGAACCCCGAGTCC CGGCCCAGGCCCCTGAGCTGGAGGGATGGAAAACTCCTCTGCAGCATCAGCCTCCTCGGAGGCAGGGAGCAGCCGCTCCCAGGAGATCGA GGAGCTGGAGCGCTTCATCGACAGCTACGTGCTGGAGTACCAGGTGCAGGGGCTGCTGGCTGACAAGACGGAGGGTGATGGCGAGAGCGA GAGGACCCAGTCCCACATCTCCCAGTGGACAGCGGACTGCAGCGAACCGCTGGACAGCAGCTGTTCCTTCTCCCGAGGGCGAGCCCCCCC ACAGCAGAATGGCAGCAAAGACAACTCTCTGGACATGCTGGGCACGGACATCTGGGCGGCCAACACCTTCGATTCCTTCAGTGGTGCCAC CTGGGACCTGCAGCCGGAAAAGCTGGACTTCACCCAGTTCCACCGCAAAGTCCGACACACGCCCAAGCAGCCCCTGCCACACATCGACCG CGAAGGGTGTGGCAAAGGGAAGCTGGAAGATGGGGATGGCATCAACCTGAATGACATCGAGAAGGTCCTTCCAGCCTGGCAGGCACAAGA CCTAAATGTCATTGAAGAAGTGATTCGAATGATGTTAGAGATCATCAACTCCTGCCTGACAAATTCCCTTCACCACAACCCAAACTTGGT ATACGCCCTGCTTTACAAACGCGATCTCTTTGAACAATTTCGAACTCATCCTTCATTTCAGGATATAATGCAAAATATTGATCTGGTGAT CTCCTTCTTTAGCTCAAGGTTGCTGCAAGCTGGAGCTGAGCTGTCAGTGGAACGGGTCCTGGAAATCATTAAGCAAGGCGTCGTTGCGCT GCCCAAAGACAGACTGAAGAAATTTCCAGAATTGAAATTCAAATATGTGGAAGAGGAGCAGCCCGAGGAGTTTTTTATCCCCTATGTCTG GTCTCTTGTCTACAACTCAGCAGTCGGCCTGTACTGGAATCCACAGGACATCCAGCTGTTCACCATGGATTCCGACTGAGGGCAGGATGC TCTCCCACCCGGACCCCTCCAGCCAAGCAGCCCTTCAAGTTCTTTTATTTCTGGGTAACAGAAGTAGACAGACAGGTTACTTGGTGTATC TTCTGTTAAAGAGGATTGCACGAGTGTGTTTTCCTCACACACTTTGATTTGGAGAATTGGTGCTAGTTGGCAATAGATAACTCAGCGTAG ATAGTATTGCAAAAAGGGGAGGAAATACACAACAATAATAAATG >20234_20234_1_CTIF-DYM_CTIF_chr18_46197115_ENST00000256413_DYM_chr18_46645296_ENST00000269445_length(amino acids)=317AA_BP=169 MENSSAASASSEAGSSRSQEIEELERFIDSYVLEYQVQGLLADKTEGDGESERTQSHISQWTADCSEPLDSSCSFSRGRAPPQQNGSKDN SLDMLGTDIWAANTFDSFSGATWDLQPEKLDFTQFHRKVRHTPKQPLPHIDREGCGKGKLEDGDGINLNDIEKVLPAWQAQDLNVIEEVI RMMLEIINSCLTNSLHHNPNLVYALLYKRDLFEQFRTHPSFQDIMQNIDLVISFFSSRLLQAGAELSVERVLEIIKQGVVALPKDRLKKF PELKFKYVEEEQPEEFFIPYVWSLVYNSAVGLYWNPQDIQLFTMDSD -------------------------------------------------------------- >20234_20234_2_CTIF-DYM_CTIF_chr18_46197115_ENST00000256413_DYM_chr18_46645296_ENST00000442713_length(transcript)=1635nt_BP=802nt CTTTCCCTGTGTCAGATCAGGGATCATTTTTTTTCCTTCCTCTACTCCCTCCCCCCTACCCGCCCCTCCCTCCCTGTTTCCCTTCCCTCC CTCCCTCCCCTCTCTGCTGGGTCTGTGCGCTGGGGCGCCCGATCCCCTCCGCAGCTGGGACGCTCCGAACTCGAGGCAGGAGTCGGCTCT CCGGAGCCTCGTCCCTCCCTTCCCCTTCCCTGCCCCCTTCCCCCACCCCCGACTCGGGCTTGGCGCGGCGGCCAGAGGAACCCCGAGTCC CGGCCCAGGCCCCTGAGCTGGAGGGATGGAAAACTCCTCTGCAGCATCAGCCTCCTCGGAGGCAGGGAGCAGCCGCTCCCAGGAGATCGA GGAGCTGGAGCGCTTCATCGACAGCTACGTGCTGGAGTACCAGGTGCAGGGGCTGCTGGCTGACAAGACGGAGGGTGATGGCGAGAGCGA GAGGACCCAGTCCCACATCTCCCAGTGGACAGCGGACTGCAGCGAACCGCTGGACAGCAGCTGTTCCTTCTCCCGAGGGCGAGCCCCCCC ACAGCAGAATGGCAGCAAAGACAACTCTCTGGACATGCTGGGCACGGACATCTGGGCGGCCAACACCTTCGATTCCTTCAGTGGTGCCAC CTGGGACCTGCAGCCGGAAAAGCTGGACTTCACCCAGTTCCACCGCAAAGTCCGACACACGCCCAAGCAGCCCCTGCCACACATCGACCG CGAAGGGTGTGGCAAAGGGAAGCTGGAAGATGGGGATGGCATCAACCTGAATGACATCGAGAAGGTCCTTCCAGCCTGGCAGGCACAAGA CCTAAATGTCATTGAAGAAGTGATTCGAATGATGTTAGAGATCATCAACTCCTGCCTGACAAATTCCCTTCACCACAACCCAAACTTGGT ATACGCCCTGCTTTACAAACGCGATCTCTTTGAACAATTTCGAACTCATCCTTCATTTCAGGATATAATGCAAAATATTGATCTGGTGAT CTCCTTCTTTAGCTCAAGGTTGCTGCAAGCTGGAGCTGAGCTGTCAGTGGAACGGGTCCTGGAAATCATTAAGCAAGGCGTCGTTGCGCT GCCCAAAGACAGACTGAAGAAATTTCCAGAATTGAAATTCAAATATGTGGAAGAGGAGCAGCCCGAGGAGTTTTTTATCCCCTATGTCTG GTCTCTTGTCTACAACTCAGCAGTCGGCCTGTACTGGAATCCACAGGACATCCAGCTGTTCACCATGGATTCCGACTGAGGGCAGGATGC TCTCCCACCCGGACCCCTCCAGCCAAGCAGCCCTTCAAGTTCTTTTATTTCTGGGTAACAGAAGTAGACAGACAGGTTACTTGGTGTATC TTCTGTTAAAGAGGATTGCACGAGTGTGTTTTCCTCACACACTTTGATTTGGAGAATTGGTGCTAGTTGGCAATAGATAACTCAGCGTAG ATAGTATTGCAAAAAGGGGAGGAAATACACAACAATAATAAATGTAAAAACCTGCTATTCAACATGCAGTTTTATTTCGAAGCCAAAAAT CTAGAGCTTTCCCAAGATCCTGTTGCCTTAGGCACATCACACTTCAACAGTGCACACTATCCAACAGTGCACACTATTCAACAGTGCACA CTATTCAAAAGCGTA >20234_20234_2_CTIF-DYM_CTIF_chr18_46197115_ENST00000256413_DYM_chr18_46645296_ENST00000442713_length(amino acids)=317AA_BP=169 MENSSAASASSEAGSSRSQEIEELERFIDSYVLEYQVQGLLADKTEGDGESERTQSHISQWTADCSEPLDSSCSFSRGRAPPQQNGSKDN SLDMLGTDIWAANTFDSFSGATWDLQPEKLDFTQFHRKVRHTPKQPLPHIDREGCGKGKLEDGDGINLNDIEKVLPAWQAQDLNVIEEVI RMMLEIINSCLTNSLHHNPNLVYALLYKRDLFEQFRTHPSFQDIMQNIDLVISFFSSRLLQAGAELSVERVLEIIKQGVVALPKDRLKKF PELKFKYVEEEQPEEFFIPYVWSLVYNSAVGLYWNPQDIQLFTMDSD -------------------------------------------------------------- >20234_20234_3_CTIF-DYM_CTIF_chr18_46197115_ENST00000382998_DYM_chr18_46645296_ENST00000269445_length(transcript)=1446nt_BP=764nt CTGTGCGCTGGGGCGCCCGATCCCCTCCGCAGCTGGGACGCTCCGAACTCGAGGCAGGAGTCGGCTCTCCGGAGCCTCGTCCCTCCCTTC CCCTTCCCTGCCCCCTTCCCCCACCCCCGACTCGGGCTTGGCGCGGCGGCCAGAGGAACCCCGAGCCCGCATTTGCTGCATCGAGCAGTT GGTTTAGTATCAGCCAAACTTGCAGCTGTTCAGACCGCGCTCCGCCGAGTCCCGGCCCAGGCCCCTGAGCTGGAGGGATGGAAAACTCCT CTGCAGCATCAGCCTCCTCGGAGGCAGGGAGCAGCCGCTCCCAGGAGATCGAGGAGCTGGAGCGCTTCATCGACAGCTACGTGCTGGAGT ACCAGGTGCAGGGGCTGCTGGCTGACAAGACGGAGGGTGATGGCGAGAGCGAGAGGACCCAGTCCCACATCTCCCAGTGGACAGCGGACT GCAGCGAACCGCTGGACAGCAGCTGTTCCTTCTCCCGAGGGCGAGCCCCCCCACAGCAGAATGGCAGCAAAGACAACTCTCTGGACATGC TGGGCACGGACATCTGGGCGGCCAACACCTTCGATTCCTTCAGTGGTGCCACCTGGGACCTGCAGCCGGAAAAGCTGGACTTCACCCAGT TCCACCGCAAAGTCCGACACACGCCCAAGCAGCCCCTGCCACACATCGACCGCGAAGGGTGTGGCAAAGGGAAGCTGGAAGATGGGGATG GCATCAACCTGAATGACATCGAGAAGGTCCTTCCAGCCTGGCAGGCACAAGACCTAAATGTCATTGAAGAAGTGATTCGAATGATGTTAG AGATCATCAACTCCTGCCTGACAAATTCCCTTCACCACAACCCAAACTTGGTATACGCCCTGCTTTACAAACGCGATCTCTTTGAACAAT TTCGAACTCATCCTTCATTTCAGGATATAATGCAAAATATTGATCTGGTGATCTCCTTCTTTAGCTCAAGGTTGCTGCAAGCTGGAGCTG AGCTGTCAGTGGAACGGGTCCTGGAAATCATTAAGCAAGGCGTCGTTGCGCTGCCCAAAGACAGACTGAAGAAATTTCCAGAATTGAAAT TCAAATATGTGGAAGAGGAGCAGCCCGAGGAGTTTTTTATCCCCTATGTCTGGTCTCTTGTCTACAACTCAGCAGTCGGCCTGTACTGGA ATCCACAGGACATCCAGCTGTTCACCATGGATTCCGACTGAGGGCAGGATGCTCTCCCACCCGGACCCCTCCAGCCAAGCAGCCCTTCAA GTTCTTTTATTTCTGGGTAACAGAAGTAGACAGACAGGTTACTTGGTGTATCTTCTGTTAAAGAGGATTGCACGAGTGTGTTTTCCTCAC ACACTTTGATTTGGAGAATTGGTGCTAGTTGGCAATAGATAACTCAGCGTAGATAGTATTGCAAAAAGGGGAGGAAATACACAACAATAA TAAATG >20234_20234_3_CTIF-DYM_CTIF_chr18_46197115_ENST00000382998_DYM_chr18_46645296_ENST00000269445_length(amino acids)=317AA_BP=169 MENSSAASASSEAGSSRSQEIEELERFIDSYVLEYQVQGLLADKTEGDGESERTQSHISQWTADCSEPLDSSCSFSRGRAPPQQNGSKDN SLDMLGTDIWAANTFDSFSGATWDLQPEKLDFTQFHRKVRHTPKQPLPHIDREGCGKGKLEDGDGINLNDIEKVLPAWQAQDLNVIEEVI RMMLEIINSCLTNSLHHNPNLVYALLYKRDLFEQFRTHPSFQDIMQNIDLVISFFSSRLLQAGAELSVERVLEIIKQGVVALPKDRLKKF PELKFKYVEEEQPEEFFIPYVWSLVYNSAVGLYWNPQDIQLFTMDSD -------------------------------------------------------------- >20234_20234_4_CTIF-DYM_CTIF_chr18_46197115_ENST00000382998_DYM_chr18_46645296_ENST00000442713_length(transcript)=1597nt_BP=764nt CTGTGCGCTGGGGCGCCCGATCCCCTCCGCAGCTGGGACGCTCCGAACTCGAGGCAGGAGTCGGCTCTCCGGAGCCTCGTCCCTCCCTTC CCCTTCCCTGCCCCCTTCCCCCACCCCCGACTCGGGCTTGGCGCGGCGGCCAGAGGAACCCCGAGCCCGCATTTGCTGCATCGAGCAGTT GGTTTAGTATCAGCCAAACTTGCAGCTGTTCAGACCGCGCTCCGCCGAGTCCCGGCCCAGGCCCCTGAGCTGGAGGGATGGAAAACTCCT CTGCAGCATCAGCCTCCTCGGAGGCAGGGAGCAGCCGCTCCCAGGAGATCGAGGAGCTGGAGCGCTTCATCGACAGCTACGTGCTGGAGT ACCAGGTGCAGGGGCTGCTGGCTGACAAGACGGAGGGTGATGGCGAGAGCGAGAGGACCCAGTCCCACATCTCCCAGTGGACAGCGGACT GCAGCGAACCGCTGGACAGCAGCTGTTCCTTCTCCCGAGGGCGAGCCCCCCCACAGCAGAATGGCAGCAAAGACAACTCTCTGGACATGC TGGGCACGGACATCTGGGCGGCCAACACCTTCGATTCCTTCAGTGGTGCCACCTGGGACCTGCAGCCGGAAAAGCTGGACTTCACCCAGT TCCACCGCAAAGTCCGACACACGCCCAAGCAGCCCCTGCCACACATCGACCGCGAAGGGTGTGGCAAAGGGAAGCTGGAAGATGGGGATG GCATCAACCTGAATGACATCGAGAAGGTCCTTCCAGCCTGGCAGGCACAAGACCTAAATGTCATTGAAGAAGTGATTCGAATGATGTTAG AGATCATCAACTCCTGCCTGACAAATTCCCTTCACCACAACCCAAACTTGGTATACGCCCTGCTTTACAAACGCGATCTCTTTGAACAAT TTCGAACTCATCCTTCATTTCAGGATATAATGCAAAATATTGATCTGGTGATCTCCTTCTTTAGCTCAAGGTTGCTGCAAGCTGGAGCTG AGCTGTCAGTGGAACGGGTCCTGGAAATCATTAAGCAAGGCGTCGTTGCGCTGCCCAAAGACAGACTGAAGAAATTTCCAGAATTGAAAT TCAAATATGTGGAAGAGGAGCAGCCCGAGGAGTTTTTTATCCCCTATGTCTGGTCTCTTGTCTACAACTCAGCAGTCGGCCTGTACTGGA ATCCACAGGACATCCAGCTGTTCACCATGGATTCCGACTGAGGGCAGGATGCTCTCCCACCCGGACCCCTCCAGCCAAGCAGCCCTTCAA GTTCTTTTATTTCTGGGTAACAGAAGTAGACAGACAGGTTACTTGGTGTATCTTCTGTTAAAGAGGATTGCACGAGTGTGTTTTCCTCAC ACACTTTGATTTGGAGAATTGGTGCTAGTTGGCAATAGATAACTCAGCGTAGATAGTATTGCAAAAAGGGGAGGAAATACACAACAATAA TAAATGTAAAAACCTGCTATTCAACATGCAGTTTTATTTCGAAGCCAAAAATCTAGAGCTTTCCCAAGATCCTGTTGCCTTAGGCACATC ACACTTCAACAGTGCACACTATCCAACAGTGCACACTATTCAACAGTGCACACTATTCAAAAGCGTA >20234_20234_4_CTIF-DYM_CTIF_chr18_46197115_ENST00000382998_DYM_chr18_46645296_ENST00000442713_length(amino acids)=317AA_BP=169 MENSSAASASSEAGSSRSQEIEELERFIDSYVLEYQVQGLLADKTEGDGESERTQSHISQWTADCSEPLDSSCSFSRGRAPPQQNGSKDN SLDMLGTDIWAANTFDSFSGATWDLQPEKLDFTQFHRKVRHTPKQPLPHIDREGCGKGKLEDGDGINLNDIEKVLPAWQAQDLNVIEEVI RMMLEIINSCLTNSLHHNPNLVYALLYKRDLFEQFRTHPSFQDIMQNIDLVISFFSSRLLQAGAELSVERVLEIIKQGVVALPKDRLKKF PELKFKYVEEEQPEEFFIPYVWSLVYNSAVGLYWNPQDIQLFTMDSD 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Fusion Gene PPI Analysis for CTIF-DYM |
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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 |
Hgene | CTIF | chr18:46197115 | chr18:46645296 | ENST00000256413 | + | 6 | 12 | 1_305 | 169.0 | 599.0 | NCBP1/CBP80 |
Hgene | CTIF | chr18:46197115 | chr18:46645296 | ENST00000382998 | + | 7 | 13 | 1_305 | 169.0 | 601.0 | NCBP1/CBP80 |
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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 CTIF-DYM |
![]() (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 CTIF-DYM |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | C0265286 | Dyggve-Melchior-Clausen syndrome | 5 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT | |
Tgene | C3888088 | SMITH-MCCORT DYSPLASIA 1 | 4 | GENOMICS_ENGLAND;UNIPROT | |
Tgene | C1846431 | SMITH-MCCORT DYSPLASIA | 2 | CTD_human;GENOMICS_ENGLAND;ORPHANET | |
Tgene | C0036341 | Schizophrenia | 1 | PSYGENET |