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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:C12orf65-SLC11A2 (FusionGDB2 ID:HG91574TG4891) |
Fusion Gene Summary for C12orf65-SLC11A2 |
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Fusion gene information | Fusion gene name: C12orf65-SLC11A2 | Fusion gene ID: hg91574tg4891 | Hgene | Tgene | Gene symbol | C12orf65 | SLC11A2 | Gene ID | 91574 | 4891 |
Gene name | chromosome 12 open reading frame 65 | solute carrier family 11 member 2 | |
Synonyms | COXPD7|SPG55 | AHMIO1|DCT1|DMT1|NRAMP2 | |
Cytomap | ('C12orf65')('SLC11A2') 12q24.31 | 12q13.12 | |
Type of gene | protein-coding | protein-coding | |
Description | probable peptide chain release factor C12orf65, mitochondrial | natural resistance-associated macrophage protein 2DMT-1NRAMP 2divalent cation transporter 1solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2solute carrier family 11 (proton-coupled divalent metal ion transporters), me | |
Modification date | 20200313 | 20200315 | |
UniProtAcc | . | . | |
Ensembl transtripts involved in fusion gene | ENST00000253233, ENST00000366329, ENST00000429587, | ||
Fusion gene scores | * DoF score | 2 X 1 X 2=4 | 4 X 3 X 4=48 |
# samples | 3 | 4 | |
** MAII score | log2(3/4*10)=2.90689059560852 | log2(4/48*10)=-0.263034405833794 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: C12orf65 [Title/Abstract] AND SLC11A2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | C12orf65(123718078)-SLC11A2(51404549), # samples:2 | ||
Anticipated loss of major functional domain due to fusion event. |
* 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 | SLC11A2 | GO:0006825 | copper ion transport | 12734107 |
Tgene | SLC11A2 | GO:0006826 | iron ion transport | 12734107|17293870 |
Tgene | SLC11A2 | GO:0006828 | manganese ion transport | 17293870 |
Tgene | SLC11A2 | GO:0015692 | lead ion transport | 12127992 |
Tgene | SLC11A2 | GO:0034755 | iron ion transmembrane transport | 17293870 |
Tgene | SLC11A2 | GO:0070574 | cadmium ion transmembrane transport | 12662899|25326704 |
![]() * 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 | LUSC | TCGA-NC-A5HJ-01A | C12orf65 | chr12 | 123718078 | - | SLC11A2 | chr12 | 51404549 | - |
ChimerDB4 | LUSC | TCGA-NC-A5HJ-01A | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
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Fusion Gene ORF analysis for C12orf65-SLC11A2 |
![]() * 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 |
5UTR-5UTR | ENST00000253233 | ENST00000262051 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
5UTR-5UTR | ENST00000253233 | ENST00000262052 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
5UTR-5UTR | ENST00000253233 | ENST00000394904 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
5UTR-5UTR | ENST00000253233 | ENST00000541174 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
5UTR-5UTR | ENST00000253233 | ENST00000546743 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
5UTR-5UTR | ENST00000253233 | ENST00000547198 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
5UTR-5UTR | ENST00000253233 | ENST00000547688 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
5UTR-intron | ENST00000253233 | ENST00000545993 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
5UTR-intron | ENST00000253233 | ENST00000549193 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000366329 | ENST00000262051 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000366329 | ENST00000262052 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000366329 | ENST00000394904 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000366329 | ENST00000541174 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000366329 | ENST00000546743 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000366329 | ENST00000547198 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000366329 | ENST00000547688 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000429587 | ENST00000262051 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000429587 | ENST00000262052 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000429587 | ENST00000394904 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000429587 | ENST00000541174 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000429587 | ENST00000546743 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000429587 | ENST00000547198 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-5UTR | ENST00000429587 | ENST00000547688 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-intron | ENST00000366329 | ENST00000545993 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-intron | ENST00000366329 | ENST00000549193 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-intron | ENST00000429587 | ENST00000545993 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
intron-intron | ENST00000429587 | ENST00000549193 | C12orf65 | chr12 | 123718078 | + | SLC11A2 | chr12 | 51404549 | - |
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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) |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
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Fusion Genomic Features for C12orf65-SLC11A2 |
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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 C12orf65-SLC11A2 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/:123718078/:51404549) - 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 |
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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: 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}. |
![]() * 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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Fusion Gene Sequence for C12orf65-SLC11A2 |
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Fusion Gene PPI Analysis for C12orf65-SLC11A2 |
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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 |
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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 C12orf65-SLC11A2 |
![]() (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 C12orf65-SLC11A2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | C12orf65 | C3150801 | COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7 | 3 | CTD_human;GENOMICS_ENGLAND;ORPHANET |
Hgene | C12orf65 | C3539506 | SPASTIC PARAPLEGIA 55, AUTOSOMAL RECESSIVE | 3 | GENOMICS_ENGLAND;ORPHANET |
Hgene | C12orf65 | C0162666 | Mitochondrial Encephalomyopathies | 1 | CTD_human |
Tgene | C3806153 | ANEMIA, HYPOCHROMIC MICROCYTIC, WITH IRON OVERLOAD 1 | 3 | GENOMICS_ENGLAND;UNIPROT | |
Tgene | C2673913 | Anemia, Hypochromic Microcytic, With Iron Overload | 2 | CTD_human;ORPHANET | |
Tgene | C0018995 | Hemochromatosis | 1 | CTD_human | |
Tgene | C0023903 | Liver neoplasms | 1 | CTD_human | |
Tgene | C0162316 | Iron deficiency anemia | 1 | CTD_human | |
Tgene | C0345904 | Malignant neoplasm of liver | 1 | CTD_human | |
Tgene | C0392514 | Hereditary hemochromatosis | 1 | CTD_human |