Fusion gene information | Fusion gene name: COL6A1-COL6A1 |
Fusion gene ID: hg1291tg1291 | | Hgene | Tgene | Gene symbol | COL6A1 | COL6A1 | Gene ID | 1291 | 1291 | Gene name | collagen type VI alpha 1 chain | collagen type VI alpha 1 chain |
Synonyms | BTHLM1|OPLL|UCHMD1 | BTHLM1|OPLL|UCHMD1 |
Cytomap | ('COL6A1')('COL6A1') 21q22.3 | 21q22.3 |
Type of gene | protein-coding | protein-coding |
Description | collagen alpha-1(VI) chainalpha 1 (VI) chain (61 AA)collagen VI, alpha-1 polypeptidecollagen, type VI, alpha 1epididymis secretory sperm binding protein | collagen alpha-1(VI) chainalpha 1 (VI) chain (61 AA)collagen VI, alpha-1 polypeptidecollagen, type VI, alpha 1epididymis secretory sperm binding protein |
Modification date | 20200328 | 20200328 |
UniProtAcc | P12109 | P12109 |
Ensembl transtripts involved in fusion gene | ENST00000498614, ENST00000361866,
| ENST00000361866, ENST00000498614,
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Fusion gene scores | * DoF score | 13 X 12 X 8=1248 | 12 X 13 X 6=936 |
# samples | 15 | 15 |
** MAII score | log2(15/1248*10)=-3.05658352836637 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(15/936*10)=-2.64154602908752 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 |
Context | PubMed: COL6A1 [Title/Abstract] AND COL6A1 [Title/Abstract] AND fusion [Title/Abstract] |
Most frequent breakpoint | COL6A1(47424555)-COL6A1(47424027), # samples:1 COL6A1(47421297)-COL6A1(47422497), # samples:1 COL6A1(47424849)-COL6A1(47424814), # samples:1
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Anticipated loss of major functional domain due to fusion event. | COL6A1-COL6A1 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. COL6A1-COL6A1 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. COL6A1-COL6A1 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. COL6A1-COL6A1 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.
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
Hgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | + | 30 | 35 | 37_235 | 652 | 1029.0 | Domain | VWFA 1 |
Hgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | + | 30 | 35 | 262_264 | 652 | 1029.0 | Motif | Note=Cell attachment site |
Hgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | + | 30 | 35 | 442_444 | 652 | 1029.0 | Motif | Note=Cell attachment site |
Hgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | + | 30 | 35 | 478_480 | 652 | 1029.0 | Motif | Note=Cell attachment site |
Hgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | + | 30 | 35 | 20_256 | 652 | 1029.0 | Region | Note=N-terminal globular domain |
Hgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | + | 30 | 35 | 257_592 | 652 | 1029.0 | Region | Note=Triple-helical region |
Tgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | | 0 | 35 | 37_235 | 0 | 1029.0 | Domain | VWFA 1 |
Tgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | | 0 | 35 | 615_805 | 0 | 1029.0 | Domain | VWFA 2 |
Tgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | | 0 | 35 | 829_1021 | 0 | 1029.0 | Domain | VWFA 3 |
Tgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | | 0 | 35 | 262_264 | 0 | 1029.0 | Motif | Note=Cell attachment site |
Tgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | | 0 | 35 | 442_444 | 0 | 1029.0 | Motif | Note=Cell attachment site |
Tgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | | 0 | 35 | 478_480 | 0 | 1029.0 | Motif | Note=Cell attachment site |
Tgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | | 0 | 35 | 20_256 | 0 | 1029.0 | Region | Note=N-terminal globular domain |
Tgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | | 0 | 35 | 257_592 | 0 | 1029.0 | Region | Note=Triple-helical region |
Tgene | COL6A1 | chr21:47421297 | chr21:47422497 | ENST00000361866 | | 0 | 35 | 593_1028 | 0 | 1029.0 | Region | Note=C-terminal globular domain |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | COL6A1 | C1834674 | BETHLEM MYOPATHY 1 | 7 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
Hgene | COL6A1 | C0410179 | Ullrich congenital muscular dystrophy 1 | 6 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Hgene | COL6A1 | C0000786 | Spontaneous abortion | 1 | CTD_human |
Hgene | COL6A1 | C0000822 | Abortion, Tubal | 1 | CTD_human |
Hgene | COL6A1 | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
Hgene | COL6A1 | C0024121 | Lung Neoplasms | 1 | CTD_human |
Hgene | COL6A1 | C0026850 | Muscular Dystrophy | 1 | CTD_human |
Hgene | COL6A1 | C0242379 | Malignant neoplasm of lung | 1 | CTD_human |
Hgene | COL6A1 | C1135196 | Heart Failure, Diastolic | 1 | CTD_human |
Hgene | COL6A1 | C3830362 | Early Pregnancy Loss | 1 | CTD_human |
Hgene | COL6A1 | C4552766 | Miscarriage | 1 | CTD_human |
Tgene | | C1834674 | BETHLEM MYOPATHY 1 | 7 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
Tgene | | C0410179 | Ullrich congenital muscular dystrophy 1 | 6 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT |
Tgene | | C0000786 | Spontaneous abortion | 1 | CTD_human |
Tgene | | C0000822 | Abortion, Tubal | 1 | CTD_human |
Tgene | | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
Tgene | | C0024121 | Lung Neoplasms | 1 | CTD_human |
Tgene | | C0026850 | Muscular Dystrophy | 1 | CTD_human |
Tgene | | C0242379 | Malignant neoplasm of lung | 1 | CTD_human |
Tgene | | C1135196 | Heart Failure, Diastolic | 1 | CTD_human |
Tgene | | C3830362 | Early Pregnancy Loss | 1 | CTD_human |
Tgene | | C4552766 | Miscarriage | 1 | CTD_human |