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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:HSPG2-VIM (FusionGDB2 ID:37875) |
Fusion Gene Summary for HSPG2-VIM |
Fusion gene summary |
Fusion gene information | Fusion gene name: HSPG2-VIM | Fusion gene ID: 37875 | Hgene | Tgene | Gene symbol | HSPG2 | VIM | Gene ID | 3339 | 7431 |
Gene name | heparan sulfate proteoglycan 2 | vimentin | |
Synonyms | HSPG|PLC|PRCAN|SJA|SJS|SJS1 | - | |
Cytomap | 1p36.12 | 10p13 | |
Type of gene | protein-coding | protein-coding | |
Description | basement membrane-specific heparan sulfate proteoglycan core proteinendorepellin (domain V region)perlecan proteoglycan | vimentinepididymis secretory sperm binding protein | |
Modification date | 20200313 | 20200327 | |
UniProtAcc | . | VMAC | |
Ensembl transtripts involved in fusion gene | ENST00000486901, ENST00000374695, ENST00000430507, | ENST00000544301, ENST00000224237, ENST00000485947, | |
Fusion gene scores | * DoF score | 22 X 23 X 12=6072 | 42 X 25 X 11=11550 |
# samples | 25 | 41 | |
** MAII score | log2(25/6072*10)=-4.60217179075338 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(41/11550*10)=-4.81612513168534 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: HSPG2 [Title/Abstract] AND VIM [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | HSPG2(22204679)-VIM(17276692), # samples:1 | ||
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) |
Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez |
Partner | Gene | GO ID | GO term | PubMed ID |
Fusion gene breakpoints across HSPG2 (5'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
Fusion gene breakpoints across VIM (3'-gene) * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0) * 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 | SKCM | TCGA-GN-A26C-01A | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
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Fusion Gene ORF analysis for HSPG2-VIM |
Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure. * 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 |
intron-3CDS | ENST00000486901 | ENST00000544301 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
intron-3CDS | ENST00000486901 | ENST00000224237 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
intron-intron | ENST00000486901 | ENST00000485947 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
In-frame | ENST00000374695 | ENST00000544301 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
In-frame | ENST00000374695 | ENST00000224237 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
5CDS-intron | ENST00000374695 | ENST00000485947 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
intron-3CDS | ENST00000430507 | ENST00000544301 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
intron-3CDS | ENST00000430507 | ENST00000224237 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
intron-intron | ENST00000430507 | ENST00000485947 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + |
ORFfinder result based on the fusion transcript sequence of in-frame fusion genes. |
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) |
ENST00000374695 | HSPG2 | chr1 | 22204679 | - | ENST00000544301 | VIM | chr10 | 17276692 | + | 3598 | 2765 | 17 | 3283 | 1088 |
ENST00000374695 | HSPG2 | chr1 | 22204679 | - | ENST00000224237 | VIM | chr10 | 17276692 | + | 3606 | 2765 | 17 | 3283 | 1088 |
DeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated. |
Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000374695 | ENST00000544301 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + | 0.002542414 | 0.99745756 |
ENST00000374695 | ENST00000224237 | HSPG2 | chr1 | 22204679 | - | VIM | chr10 | 17276692 | + | 0.002518384 | 0.99748164 |
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Fusion Genomic Features for HSPG2-VIM |
FusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints. |
Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
HSPG2 | chr1 | 22204678 | - | VIM | chr10 | 17276691 | + | 2.90E-05 | 0.99997103 |
HSPG2 | chr1 | 22204678 | - | VIM | chr10 | 17276691 | + | 2.90E-05 | 0.99997103 |
Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page. |
Distribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page. |
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Fusion Protein Features for HSPG2-VIM |
Go to FGviewer for the breakpoints of chr1:22204679-chr10:17276692 - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. |
Main function of each fusion partner protein. (from UniProt) |
Hgene | Tgene |
. | VIM |
FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes. | 169 |
Retention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at * 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 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 198_235 | 895.0 | 4392.0 | Domain | LDL-receptor class A 1 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 284_320 | 895.0 | 4392.0 | Domain | LDL-receptor class A 2 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 324_360 | 895.0 | 4392.0 | Domain | LDL-receptor class A 3 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 367_404 | 895.0 | 4392.0 | Domain | LDL-receptor class A 4 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 405_504 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 1 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 521_530 | 895.0 | 4392.0 | Domain | Laminin EGF-like 1%3B first part |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 538_730 | 895.0 | 4392.0 | Domain | Laminin IV type A 1 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 731_763 | 895.0 | 4392.0 | Domain | Laminin EGF-like 1%3B second part |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 764_813 | 895.0 | 4392.0 | Domain | Laminin EGF-like 2 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 80_191 | 895.0 | 4392.0 | Domain | SEA |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 814_871 | 895.0 | 4392.0 | Domain | Laminin EGF-like 3 |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 303_407 | 294.0 | 467.0 | Coiled coil | Ontology_term=ECO:0000269 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 303_407 | 294.0 | 467.0 | Coiled coil | Ontology_term=ECO:0000269 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 326_329 | 294.0 | 467.0 | Motif | [IL]-x-C-x-x-[DE] motif | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 326_329 | 294.0 | 467.0 | Motif | [IL]-x-C-x-x-[DE] motif | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 408_466 | 294.0 | 467.0 | Region | Note=Tail | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 408_466 | 294.0 | 467.0 | Region | Note=Tail |
- 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 | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1126_1158 | 895.0 | 4392.0 | Domain | Laminin EGF-like 5%3B second part |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1159_1208 | 895.0 | 4392.0 | Domain | Laminin EGF-like 6 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1209_1265 | 895.0 | 4392.0 | Domain | Laminin EGF-like 7 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1275_1324 | 895.0 | 4392.0 | Domain | Laminin EGF-like 8 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1325_1334 | 895.0 | 4392.0 | Domain | Laminin EGF-like 9%3B first part |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1344_1529 | 895.0 | 4392.0 | Domain | Laminin IV type A 3 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1530_1562 | 895.0 | 4392.0 | Domain | Laminin EGF-like 9%3B second part |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1563_1612 | 895.0 | 4392.0 | Domain | Laminin EGF-like 10 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1613_1670 | 895.0 | 4392.0 | Domain | Laminin EGF-like 11 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1677_1771 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 2 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1772_1865 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 3 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1866_1955 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 4 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 1956_2051 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 5 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2052_2151 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 6 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2152_2244 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 7 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2245_2340 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 8 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2341_2436 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 9 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2437_2533 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 10 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2534_2629 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 11 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2630_2726 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 12 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2727_2826 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 13 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2827_2924 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 14 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 2925_3021 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 15 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3022_3112 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 16 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3113_3211 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 17 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3212_3298 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 18 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3299_3399 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 19 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3400_3488 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 20 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3489_3574 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 21 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3575_3662 | 895.0 | 4392.0 | Domain | Note=Ig-like C2-type 22 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3663_3843 | 895.0 | 4392.0 | Domain | Laminin G-like 1 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3844_3881 | 895.0 | 4392.0 | Domain | EGF-like 1 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3884_3922 | 895.0 | 4392.0 | Domain | EGF-like 2 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 3928_4103 | 895.0 | 4392.0 | Domain | Laminin G-like 2 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 4104_4141 | 895.0 | 4392.0 | Domain | EGF-like 3 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 4143_4176 | 895.0 | 4392.0 | Domain | EGF-like 4 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 4201_4389 | 895.0 | 4392.0 | Domain | Laminin G-like 3 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 879_923 | 895.0 | 4392.0 | Domain | Laminin EGF-like 4%3B truncated |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 924_933 | 895.0 | 4392.0 | Domain | Laminin EGF-like 5%3B first part |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 941_1125 | 895.0 | 4392.0 | Domain | Laminin IV type A 2 |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 4149_4151 | 895.0 | 4392.0 | Region | Mediates motor neuron attachment |
Hgene | HSPG2 | chr1:22204679 | chr10:17276692 | ENST00000374695 | - | 21 | 97 | 4299_4301 | 895.0 | 4392.0 | Region | Mediates motor neuron attachment |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 154_245 | 294.0 | 467.0 | Coiled coil | Ontology_term=ECO:0000269 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 96_131 | 294.0 | 467.0 | Coiled coil | Ontology_term=ECO:0000269 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 154_245 | 294.0 | 467.0 | Coiled coil | Ontology_term=ECO:0000269 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 96_131 | 294.0 | 467.0 | Coiled coil | Ontology_term=ECO:0000269 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 103_411 | 294.0 | 467.0 | Domain | IF rod | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 103_411 | 294.0 | 467.0 | Domain | IF rod | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 132_153 | 294.0 | 467.0 | Region | Note=Linker 1 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 246_268 | 294.0 | 467.0 | Region | Note=Linker 12 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 269_407 | 294.0 | 467.0 | Region | Note=Coil 2 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000224237 | 3 | 9 | 2_95 | 294.0 | 467.0 | Region | Note=Head | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 132_153 | 294.0 | 467.0 | Region | Note=Linker 1 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 246_268 | 294.0 | 467.0 | Region | Note=Linker 12 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 269_407 | 294.0 | 467.0 | Region | Note=Coil 2 | |
Tgene | VIM | chr1:22204679 | chr10:17276692 | ENST00000544301 | 4 | 10 | 2_95 | 294.0 | 467.0 | Region | Note=Head |
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Fusion Gene Sequence for HSPG2-VIM |
For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones. |
>In-frame_ENST00000374695_ENST00000544301_TCGA-GN-A26C-01A_HSPG2_chr1_22204679_-_VIM_chr10_17276692_length(transcript)=3598nt_BP=2765nt GGCCGGCGAGCGGGCGGCTGCGGGCGGCGCGGAGCGGGCGGCGCGGAGCGAGCGAGCGAGAGAGCGGCGCGGGCCGGGCCATGGGGTGGC GGGCGGCGGGCGCGCTGCTGCTGGCGCTGCTGCTGCACGGGCGGCTGCTGGCGGTGACCCATGGGCTGAGGGCATACGATGGCTTGTCTC TGCCTGAGGACATAGAGACCGTCACAGCAAGCCAAATGCGCTGGACACATTCGTACCTTTCTGATGATGAGGACATGCTGGCTGACAGCA TCTCAGGAGACGACCTGGGCAGTGGGGACCTGGGCAGCGGGGACTTCCAGATGGTTTATTTCCGAGCCCTGGTGAATTTCACTCGCTCCA TCGAGTACAGCCCTCAGCTGGAGGATGCAGGCTCCAGAGAGTTCCGAGAGGTGTCCGAGGCTGTGGTAGACACGCTGGAGTCGGAGTACT TGAAAATTCCCGGAGACCAGGTTGTCAGTGTGGTGTTCATCAAGGAGCTGGATGGCTGGGTTTTTGTGGAGCTGGATGTGGGCTCGGAAG GGAATGCGGATGGGGCTCAGATTCAGGAGATGCTGCTCAGGGTCATCTCCAGCGGCTCTGTGGCCTCCTACGTCACCTCTCCCCAGGGAT TCCAGTTCCGACGCCTGGGCACAGTGCCCCAGTTCCCAAGAGCCTGCACGGAGGCCGAGTTTGCCTGCCACAGCTACAATGAGTGTGTGG CCCTGGAGTATCGCTGTGACCGGCGGCCCGACTGCAGGGACATGTCTGATGAGCTCAATTGTGAGGAGCCAGTCCTGGGTATCAGCCCCA CATTCTCTCTCCTTGTGGAGACGACATCTTTACCGCCCCGGCCAGAGACAACCATCATGCGACAGCCACCAGTCACCCACGCTCCTCAGC CCCTGCTTCCCGGTTCCGTCAGGCCCCTGCCCTGTGGGCCCCAGGAGGCCGCATGCCGCAATGGGCACTGCATCCCCAGAGACTACCTCT GCGACGGACAGGAGGACTGCGAGGACGGCAGCGATGAGCTAGACTGTGGCCCCCCGCCACCCTGTGAGCCCAACGAGTTCCCCTGCGGGA ATGGACATTGTGCCCTCAAGCTGTGGCGCTGCGATGGTGACTTTGACTGTGAGGACCGAACTGATGAAGCCAACTGCCCCACCAAGCGTC CTGAGGAAGTGTGCGGGCCCACACAGTTCCGATGCGTCTCTACCAACATGTGCATCCCAGCCAGCTTCCACTGTGACGAGGAGAGCGACT GTCCTGACCGGAGCGACGAGTTTGGCTGCATGCCCCCCCAGGTGGTGACACCTCCCCGGGAGTCCATCCAGGCTTCCCGGGGCCAGACAG TGACCTTCACCTGCGTGGCCATTGGCGTCCCCACCCCCATCATCAATTGGAGGCTCAACTGGGGCCACATCCCCTCTCATCCCAGGGTGA CAGTGACCAGCGAGGGTGGCCGTGGCACACTGATCATCCGTGATGTGAAGGAGTCAGACCAGGGTGCCTACACCTGTGAGGCCATGAACG CCCGGGGCATGGTGTTTGGCATTCCTGACGGTGTCCTTGAGCTCGTCCCACAACGAGGCCCCTGCCCTGACGGCCACTTCTACCTGGAGC ACAGCGCCGCCTGCCTGCCCTGCTTCTGCTTTGGCATCACCAGCGTGTGCCAGAGCACCCGCCGCTTCCGGGACCAGATCAGGCTGCGCT TTGACCAACCCGATGACTTCAAGGGTGTGAATGTGACAATGCCTGCGCAGCCCGGCACGCCACCCCTCTCCTCCACGCAGCTGCAGATCG ACCCATCCCTGCACGAGTTCCAGCTAGTCGACCTGTCCCGCCGCTTCCTCGTCCACGACTCCTTCTGGGCTCTGCCTGAACAGTTCCTGG GCAACAAGGTGGACTCCTATGGCGGCTCCCTGCGTTACAACGTGCGCTACGAGTTGGCCCGTGGCATGCTGGAGCCAGTGCAGCGGCCGG ACGTGGTCCTCATGGGTGCCGGGTACCGCCTCCTCTCCCGAGGCCACACACCCACCCAACCTGGTGCTCTGAACCAGCGCCAGGTCCAGT TCTCTGAGGAGCACTGGGTCCATGAGTCTGGCCGGCCGGTGCAGCGCGCGGAGCTGCTGCAGGTGCTGCAGAGCCTGGAGGCCGTGCTCA TCCAGACCGTGTACAACACCAAGATGGCCAGCGTGGGACTTAGCGACATCGCCATGGATACCACCGTCACCCATGCCACCAGCCATGGCC GTGCCCACAGTGTGGAGGAGTGCAGATGCCCCATTGGCTATTCTGGCTTGTCCTGCGAGAGCTGTGATGCCCACTTCACTCGGGTGCCTG GTGGGCCCTACCTGGGCACCTGCTCTGGTTGCAATTGCAATGGCCATGCCAGCTCCTGTGACCCTGTGTATGGCCACTGCCTGAATTGCC AGCACAACACGGAGGGGCCACAGTGCAACAAGTGCAAGGCTGGCTTCTTTGGGGACGCCATGAAGGCCACGGCCACTTCCTGCCGGCCCT GCCCTTGCCCATACATCGATGCCTCCCGCAGATTCTCAGACACTTGCTTCCTGGACACGGATGGCCAAGCCACATGTGACGCCTGTGCCC CAGGCTACACTGGCCGCCGCTGTGAGAGCTGTGCCCCCGGATACGAGGGCAACCCCATCCAGCCCGGCGGGAAGTGCAGGCCCGTCAACC AGGAGATTGTGCGCTGTGACGAGCGTGGCAGCATGGGGACCTCCGGGGAGGCCTGCCGCTGTAAGTTTGCTGACCTCTCTGAGGCTGCCA ACCGGAACAATGACGCCCTGCGCCAGGCAAAGCAGGAGTCCACTGAGTACCGGAGACAGGTGCAGTCCCTCACCTGTGAAGTGGATGCCC TTAAAGGAACCAATGAGTCCCTGGAACGCCAGATGCGTGAAATGGAAGAGAACTTTGCCGTTGAAGCTGCTAACTACCAAGACACTATTG GCCGCCTGCAGGATGAGATTCAGAATATGAAGGAGGAAATGGCTCGTCACCTTCGTGAATACCAAGACCTGCTCAATGTTAAGATGGCCC TTGACATTGAGATTGCCACCTACAGGAAGCTGCTGGAAGGCGAGGAGAGCAGGATTTCTCTGCCTCTTCCAAACTTTTCCTCCCTGAACC TGAGGGAAACTAATCTGGATTCACTCCCTCTGGTTGATACCCACTCAAAAAGGACACTTCTGATTAAGACGGTTGAAACTAGAGATGGAC AGGTTATCAACGAAACTTCTCAGCATCACGATGACCTTGAATAAAAATTGCACACACTCAGTGCAGCAATATATTACCAGCAAGAATAAA AAAGAAATCCATATCTTAAAGAAACAGCTTTCAAGTGCCTTTCTGCAGTTTTTCAGGAGCGCAAGATAGATTTGGAATAGGAATAAGCTC TAGTTCTTAACAACCGACACTCCTACAAGATTTAGAAAAAAGTTTACAACATAATCTAGTTTACAGAAAAATCTTGTGCTAGAATACTTT >In-frame_ENST00000374695_ENST00000544301_TCGA-GN-A26C-01A_HSPG2_chr1_22204679_-_VIM_chr10_17276692_length(amino acids)=1088AA_start in transcript=17_stop in transcript=3283 MRAARSGRRGASERESGAGRAMGWRAAGALLLALLLHGRLLAVTHGLRAYDGLSLPEDIETVTASQMRWTHSYLSDDEDMLADSISGDDL GSGDLGSGDFQMVYFRALVNFTRSIEYSPQLEDAGSREFREVSEAVVDTLESEYLKIPGDQVVSVVFIKELDGWVFVELDVGSEGNADGA QIQEMLLRVISSGSVASYVTSPQGFQFRRLGTVPQFPRACTEAEFACHSYNECVALEYRCDRRPDCRDMSDELNCEEPVLGISPTFSLLV ETTSLPPRPETTIMRQPPVTHAPQPLLPGSVRPLPCGPQEAACRNGHCIPRDYLCDGQEDCEDGSDELDCGPPPPCEPNEFPCGNGHCAL KLWRCDGDFDCEDRTDEANCPTKRPEEVCGPTQFRCVSTNMCIPASFHCDEESDCPDRSDEFGCMPPQVVTPPRESIQASRGQTVTFTCV AIGVPTPIINWRLNWGHIPSHPRVTVTSEGGRGTLIIRDVKESDQGAYTCEAMNARGMVFGIPDGVLELVPQRGPCPDGHFYLEHSAACL PCFCFGITSVCQSTRRFRDQIRLRFDQPDDFKGVNVTMPAQPGTPPLSSTQLQIDPSLHEFQLVDLSRRFLVHDSFWALPEQFLGNKVDS YGGSLRYNVRYELARGMLEPVQRPDVVLMGAGYRLLSRGHTPTQPGALNQRQVQFSEEHWVHESGRPVQRAELLQVLQSLEAVLIQTVYN TKMASVGLSDIAMDTTVTHATSHGRAHSVEECRCPIGYSGLSCESCDAHFTRVPGGPYLGTCSGCNCNGHASSCDPVYGHCLNCQHNTEG PQCNKCKAGFFGDAMKATATSCRPCPCPYIDASRRFSDTCFLDTDGQATCDACAPGYTGRRCESCAPGYEGNPIQPGGKCRPVNQEIVRC DERGSMGTSGEACRCKFADLSEAANRNNDALRQAKQESTEYRRQVQSLTCEVDALKGTNESLERQMREMEENFAVEAANYQDTIGRLQDE IQNMKEEMARHLREYQDLLNVKMALDIEIATYRKLLEGEESRISLPLPNFSSLNLRETNLDSLPLVDTHSKRTLLIKTVETRDGQVINET -------------------------------------------------------------- >In-frame_ENST00000374695_ENST00000224237_TCGA-GN-A26C-01A_HSPG2_chr1_22204679_-_VIM_chr10_17276692_length(transcript)=3606nt_BP=2765nt GGCCGGCGAGCGGGCGGCTGCGGGCGGCGCGGAGCGGGCGGCGCGGAGCGAGCGAGCGAGAGAGCGGCGCGGGCCGGGCCATGGGGTGGC GGGCGGCGGGCGCGCTGCTGCTGGCGCTGCTGCTGCACGGGCGGCTGCTGGCGGTGACCCATGGGCTGAGGGCATACGATGGCTTGTCTC TGCCTGAGGACATAGAGACCGTCACAGCAAGCCAAATGCGCTGGACACATTCGTACCTTTCTGATGATGAGGACATGCTGGCTGACAGCA TCTCAGGAGACGACCTGGGCAGTGGGGACCTGGGCAGCGGGGACTTCCAGATGGTTTATTTCCGAGCCCTGGTGAATTTCACTCGCTCCA TCGAGTACAGCCCTCAGCTGGAGGATGCAGGCTCCAGAGAGTTCCGAGAGGTGTCCGAGGCTGTGGTAGACACGCTGGAGTCGGAGTACT TGAAAATTCCCGGAGACCAGGTTGTCAGTGTGGTGTTCATCAAGGAGCTGGATGGCTGGGTTTTTGTGGAGCTGGATGTGGGCTCGGAAG GGAATGCGGATGGGGCTCAGATTCAGGAGATGCTGCTCAGGGTCATCTCCAGCGGCTCTGTGGCCTCCTACGTCACCTCTCCCCAGGGAT TCCAGTTCCGACGCCTGGGCACAGTGCCCCAGTTCCCAAGAGCCTGCACGGAGGCCGAGTTTGCCTGCCACAGCTACAATGAGTGTGTGG CCCTGGAGTATCGCTGTGACCGGCGGCCCGACTGCAGGGACATGTCTGATGAGCTCAATTGTGAGGAGCCAGTCCTGGGTATCAGCCCCA CATTCTCTCTCCTTGTGGAGACGACATCTTTACCGCCCCGGCCAGAGACAACCATCATGCGACAGCCACCAGTCACCCACGCTCCTCAGC CCCTGCTTCCCGGTTCCGTCAGGCCCCTGCCCTGTGGGCCCCAGGAGGCCGCATGCCGCAATGGGCACTGCATCCCCAGAGACTACCTCT GCGACGGACAGGAGGACTGCGAGGACGGCAGCGATGAGCTAGACTGTGGCCCCCCGCCACCCTGTGAGCCCAACGAGTTCCCCTGCGGGA ATGGACATTGTGCCCTCAAGCTGTGGCGCTGCGATGGTGACTTTGACTGTGAGGACCGAACTGATGAAGCCAACTGCCCCACCAAGCGTC CTGAGGAAGTGTGCGGGCCCACACAGTTCCGATGCGTCTCTACCAACATGTGCATCCCAGCCAGCTTCCACTGTGACGAGGAGAGCGACT GTCCTGACCGGAGCGACGAGTTTGGCTGCATGCCCCCCCAGGTGGTGACACCTCCCCGGGAGTCCATCCAGGCTTCCCGGGGCCAGACAG TGACCTTCACCTGCGTGGCCATTGGCGTCCCCACCCCCATCATCAATTGGAGGCTCAACTGGGGCCACATCCCCTCTCATCCCAGGGTGA CAGTGACCAGCGAGGGTGGCCGTGGCACACTGATCATCCGTGATGTGAAGGAGTCAGACCAGGGTGCCTACACCTGTGAGGCCATGAACG CCCGGGGCATGGTGTTTGGCATTCCTGACGGTGTCCTTGAGCTCGTCCCACAACGAGGCCCCTGCCCTGACGGCCACTTCTACCTGGAGC ACAGCGCCGCCTGCCTGCCCTGCTTCTGCTTTGGCATCACCAGCGTGTGCCAGAGCACCCGCCGCTTCCGGGACCAGATCAGGCTGCGCT TTGACCAACCCGATGACTTCAAGGGTGTGAATGTGACAATGCCTGCGCAGCCCGGCACGCCACCCCTCTCCTCCACGCAGCTGCAGATCG ACCCATCCCTGCACGAGTTCCAGCTAGTCGACCTGTCCCGCCGCTTCCTCGTCCACGACTCCTTCTGGGCTCTGCCTGAACAGTTCCTGG GCAACAAGGTGGACTCCTATGGCGGCTCCCTGCGTTACAACGTGCGCTACGAGTTGGCCCGTGGCATGCTGGAGCCAGTGCAGCGGCCGG ACGTGGTCCTCATGGGTGCCGGGTACCGCCTCCTCTCCCGAGGCCACACACCCACCCAACCTGGTGCTCTGAACCAGCGCCAGGTCCAGT TCTCTGAGGAGCACTGGGTCCATGAGTCTGGCCGGCCGGTGCAGCGCGCGGAGCTGCTGCAGGTGCTGCAGAGCCTGGAGGCCGTGCTCA TCCAGACCGTGTACAACACCAAGATGGCCAGCGTGGGACTTAGCGACATCGCCATGGATACCACCGTCACCCATGCCACCAGCCATGGCC GTGCCCACAGTGTGGAGGAGTGCAGATGCCCCATTGGCTATTCTGGCTTGTCCTGCGAGAGCTGTGATGCCCACTTCACTCGGGTGCCTG GTGGGCCCTACCTGGGCACCTGCTCTGGTTGCAATTGCAATGGCCATGCCAGCTCCTGTGACCCTGTGTATGGCCACTGCCTGAATTGCC AGCACAACACGGAGGGGCCACAGTGCAACAAGTGCAAGGCTGGCTTCTTTGGGGACGCCATGAAGGCCACGGCCACTTCCTGCCGGCCCT GCCCTTGCCCATACATCGATGCCTCCCGCAGATTCTCAGACACTTGCTTCCTGGACACGGATGGCCAAGCCACATGTGACGCCTGTGCCC CAGGCTACACTGGCCGCCGCTGTGAGAGCTGTGCCCCCGGATACGAGGGCAACCCCATCCAGCCCGGCGGGAAGTGCAGGCCCGTCAACC AGGAGATTGTGCGCTGTGACGAGCGTGGCAGCATGGGGACCTCCGGGGAGGCCTGCCGCTGTAAGTTTGCTGACCTCTCTGAGGCTGCCA ACCGGAACAATGACGCCCTGCGCCAGGCAAAGCAGGAGTCCACTGAGTACCGGAGACAGGTGCAGTCCCTCACCTGTGAAGTGGATGCCC TTAAAGGAACCAATGAGTCCCTGGAACGCCAGATGCGTGAAATGGAAGAGAACTTTGCCGTTGAAGCTGCTAACTACCAAGACACTATTG GCCGCCTGCAGGATGAGATTCAGAATATGAAGGAGGAAATGGCTCGTCACCTTCGTGAATACCAAGACCTGCTCAATGTTAAGATGGCCC TTGACATTGAGATTGCCACCTACAGGAAGCTGCTGGAAGGCGAGGAGAGCAGGATTTCTCTGCCTCTTCCAAACTTTTCCTCCCTGAACC TGAGGGAAACTAATCTGGATTCACTCCCTCTGGTTGATACCCACTCAAAAAGGACACTTCTGATTAAGACGGTTGAAACTAGAGATGGAC AGGTTATCAACGAAACTTCTCAGCATCACGATGACCTTGAATAAAAATTGCACACACTCAGTGCAGCAATATATTACCAGCAAGAATAAA AAAGAAATCCATATCTTAAAGAAACAGCTTTCAAGTGCCTTTCTGCAGTTTTTCAGGAGCGCAAGATAGATTTGGAATAGGAATAAGCTC TAGTTCTTAACAACCGACACTCCTACAAGATTTAGAAAAAAGTTTACAACATAATCTAGTTTACAGAAAAATCTTGTGCTAGAATACTTT TTAAAAGGTATTTTGAATACCATTAAAACTGCTTTTTTTTTTCCAGCAAGTATCCAACCAACTTGGTTCTGCTTCAATAAATCTTTGGAA >In-frame_ENST00000374695_ENST00000224237_TCGA-GN-A26C-01A_HSPG2_chr1_22204679_-_VIM_chr10_17276692_length(amino acids)=1088AA_start in transcript=17_stop in transcript=3283 MRAARSGRRGASERESGAGRAMGWRAAGALLLALLLHGRLLAVTHGLRAYDGLSLPEDIETVTASQMRWTHSYLSDDEDMLADSISGDDL GSGDLGSGDFQMVYFRALVNFTRSIEYSPQLEDAGSREFREVSEAVVDTLESEYLKIPGDQVVSVVFIKELDGWVFVELDVGSEGNADGA QIQEMLLRVISSGSVASYVTSPQGFQFRRLGTVPQFPRACTEAEFACHSYNECVALEYRCDRRPDCRDMSDELNCEEPVLGISPTFSLLV ETTSLPPRPETTIMRQPPVTHAPQPLLPGSVRPLPCGPQEAACRNGHCIPRDYLCDGQEDCEDGSDELDCGPPPPCEPNEFPCGNGHCAL KLWRCDGDFDCEDRTDEANCPTKRPEEVCGPTQFRCVSTNMCIPASFHCDEESDCPDRSDEFGCMPPQVVTPPRESIQASRGQTVTFTCV AIGVPTPIINWRLNWGHIPSHPRVTVTSEGGRGTLIIRDVKESDQGAYTCEAMNARGMVFGIPDGVLELVPQRGPCPDGHFYLEHSAACL PCFCFGITSVCQSTRRFRDQIRLRFDQPDDFKGVNVTMPAQPGTPPLSSTQLQIDPSLHEFQLVDLSRRFLVHDSFWALPEQFLGNKVDS YGGSLRYNVRYELARGMLEPVQRPDVVLMGAGYRLLSRGHTPTQPGALNQRQVQFSEEHWVHESGRPVQRAELLQVLQSLEAVLIQTVYN TKMASVGLSDIAMDTTVTHATSHGRAHSVEECRCPIGYSGLSCESCDAHFTRVPGGPYLGTCSGCNCNGHASSCDPVYGHCLNCQHNTEG PQCNKCKAGFFGDAMKATATSCRPCPCPYIDASRRFSDTCFLDTDGQATCDACAPGYTGRRCESCAPGYEGNPIQPGGKCRPVNQEIVRC DERGSMGTSGEACRCKFADLSEAANRNNDALRQAKQESTEYRRQVQSLTCEVDALKGTNESLERQMREMEENFAVEAANYQDTIGRLQDE IQNMKEEMARHLREYQDLLNVKMALDIEIATYRKLLEGEESRISLPLPNFSSLNLRETNLDSLPLVDTHSKRTLLIKTVETRDGQVINET -------------------------------------------------------------- |
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Fusion Gene PPI Analysis for HSPG2-VIM |
Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in |
Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160) |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
- Retained PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
- Lost PPIs in in-frame fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
- Retained PPIs, but lost function due to frame-shift fusion. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Related Drugs for HSPG2-VIM |
Drugs targeting genes involved in this fusion gene. (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 HSPG2-VIM |
Diseases associated with fusion partners. (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | HSPG2 | C0036391 | Schwartz-Jampel Syndrome | 3 | CTD_human;GENOMICS_ENGLAND;ORPHANET |
Hgene | HSPG2 | C4551479 | Schwartz-Jampel Syndrome, Type 1 | 3 | CTD_human;GENOMICS_ENGLAND;UNIPROT |
Hgene | HSPG2 | C0013366 | Dyschondroplasias | 2 | CTD_human |
Hgene | HSPG2 | C0025237 | Melnick-Needles Syndrome | 2 | CTD_human |
Hgene | HSPG2 | C0026760 | Multiple Epiphyseal Dysplasia | 2 | CTD_human |
Hgene | HSPG2 | C0029422 | Osteochondrodysplasias | 2 | CTD_human |
Hgene | HSPG2 | C0038015 | Spondyloepiphyseal Dysplasia | 2 | CTD_human |
Hgene | HSPG2 | C0432272 | Van Buchem disease | 2 | CTD_human |
Hgene | HSPG2 | C3541456 | Spondyloepiphyseal Dysplasia Tarda, X-Linked | 2 | CTD_human |
Hgene | HSPG2 | C0004238 | Atrial Fibrillation | 1 | CTD_human |
Hgene | HSPG2 | C0235480 | Paroxysmal atrial fibrillation | 1 | CTD_human |
Hgene | HSPG2 | C0376634 | Craniofacial Abnormalities | 1 | CTD_human |
Hgene | HSPG2 | C1857100 | Dyssegmental dysplasia | 1 | CTD_human;GENOMICS_ENGLAND;ORPHANET |
Hgene | HSPG2 | C2585653 | Persistent atrial fibrillation | 1 | CTD_human |
Hgene | HSPG2 | C3468561 | familial atrial fibrillation | 1 | CTD_human |
Tgene | VIM | C0006142 | Malignant neoplasm of breast | 4 | CTD_human |
Tgene | VIM | C0678222 | Breast Carcinoma | 4 | CTD_human |
Tgene | VIM | C1257931 | Mammary Neoplasms, Human | 4 | CTD_human |
Tgene | VIM | C1458155 | Mammary Neoplasms | 4 | CTD_human |
Tgene | VIM | C3805411 | CATARACT 30 | 4 | GENOMICS_ENGLAND;UNIPROT |
Tgene | VIM | C4704874 | Mammary Carcinoma, Human | 4 | CTD_human |
Tgene | VIM | C0023890 | Liver Cirrhosis | 2 | CTD_human |
Tgene | VIM | C0029408 | Degenerative polyarthritis | 2 | CTD_human |
Tgene | VIM | C0033578 | Prostatic Neoplasms | 2 | CTD_human |
Tgene | VIM | C0086743 | Osteoarthrosis Deformans | 2 | CTD_human |
Tgene | VIM | C0239946 | Fibrosis, Liver | 2 | CTD_human |
Tgene | VIM | C0376358 | Malignant neoplasm of prostate | 2 | CTD_human |
Tgene | VIM | C0007140 | Carcinosarcoma | 1 | CTD_human |
Tgene | VIM | C0007621 | Neoplastic Cell Transformation | 1 | CTD_human |
Tgene | VIM | C0019193 | Hepatitis, Toxic | 1 | CTD_human |
Tgene | VIM | C0023893 | Liver Cirrhosis, Experimental | 1 | CTD_human |
Tgene | VIM | C0027626 | Neoplasm Invasiveness | 1 | CTD_human |
Tgene | VIM | C0027627 | Neoplasm Metastasis | 1 | CTD_human |
Tgene | VIM | C0027720 | Nephrosis | 1 | CTD_human |
Tgene | VIM | C0031149 | Peritoneal Neoplasms | 1 | CTD_human |
Tgene | VIM | C0035126 | Reperfusion Injury | 1 | CTD_human |
Tgene | VIM | C0035309 | Retinal Diseases | 1 | CTD_human |
Tgene | VIM | C0039101 | synovial sarcoma | 1 | CTD_human |
Tgene | VIM | C0043094 | Weight Gain | 1 | CTD_human |
Tgene | VIM | C0085084 | Motor Neuron Disease | 1 | CTD_human |
Tgene | VIM | C0086543 | Cataract | 1 | CTD_human |
Tgene | VIM | C0154681 | Anterior Horn Cell Disease | 1 | CTD_human |
Tgene | VIM | C0154682 | Lateral Sclerosis | 1 | CTD_human |
Tgene | VIM | C0270715 | Degenerative Diseases, Central Nervous System | 1 | CTD_human |
Tgene | VIM | C0270763 | Familial Motor Neuron Disease | 1 | CTD_human |
Tgene | VIM | C0270764 | Motor Neuron Disease, Lower | 1 | CTD_human |
Tgene | VIM | C0345967 | Malignant mesothelioma | 1 | CTD_human |
Tgene | VIM | C0346990 | Carcinomatosis of peritoneal cavity | 1 | CTD_human |
Tgene | VIM | C0521659 | Motor Neuron Disease, Upper | 1 | CTD_human |
Tgene | VIM | C0524524 | Pseudoaphakia | 1 | CTD_human |
Tgene | VIM | C0524851 | Neurodegenerative Disorders | 1 | CTD_human |
Tgene | VIM | C0543858 | Motor Neuron Disease, Secondary | 1 | CTD_human |
Tgene | VIM | C0751733 | Degenerative Diseases, Spinal Cord | 1 | CTD_human |
Tgene | VIM | C0860207 | Drug-Induced Liver Disease | 1 | CTD_human |
Tgene | VIM | C0948089 | Acute Coronary Syndrome | 1 | CTD_human |
Tgene | VIM | C1262760 | Hepatitis, Drug-Induced | 1 | CTD_human |
Tgene | VIM | C1510497 | Lens Opacities | 1 | CTD_human |
Tgene | VIM | C1833118 | Cataract, Pulverulent | 1 | ORPHANET |
Tgene | VIM | C1852438 | CATARACT, COPPOCK-LIKE | 1 | ORPHANET |
Tgene | VIM | C1862939 | AMYOTROPHIC LATERAL SCLEROSIS 1 | 1 | CTD_human |
Tgene | VIM | C1862941 | Amyotrophic Lateral Sclerosis, Sporadic | 1 | CTD_human |
Tgene | VIM | C3658290 | Drug-Induced Acute Liver Injury | 1 | CTD_human |
Tgene | VIM | C4277682 | Chemical and Drug Induced Liver Injury | 1 | CTD_human |
Tgene | VIM | C4279912 | Chemically-Induced Liver Toxicity | 1 | CTD_human |
Tgene | VIM | C4551993 | Amyotrophic Lateral Sclerosis, Familial | 1 | CTD_human |