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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:FAM98C-SPINT2 (FusionGDB2 ID:HG147965TG10653) |
Fusion Gene Summary for FAM98C-SPINT2 |
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Fusion gene information | Fusion gene name: FAM98C-SPINT2 | Fusion gene ID: hg147965tg10653 | Hgene | Tgene | Gene symbol | FAM98C | SPINT2 | Gene ID | 147965 | 10653 |
Gene name | family with sequence similarity 98 member C | serine peptidase inhibitor, Kunitz type 2 | |
Synonyms | - | DIAR3|HAI-2|HAI2|Kop|PB | |
Cytomap | ('FAM98C')('SPINT2') 19q13.2 | 19q13.2 | |
Type of gene | protein-coding | protein-coding | |
Description | protein FAM98C | kunitz-type protease inhibitor 2hepatocyte growth factor activator inhibitor type 2serine protease inhibitor, Kunitz type, 2testicular tissue protein Li 183 | |
Modification date | 20200313 | 20200315 | |
UniProtAcc | Q17RN3 | . | |
Ensembl transtripts involved in fusion gene | ENST00000585954, ENST00000252530, ENST00000343358, ENST00000588262, | ||
Fusion gene scores | * DoF score | 5 X 3 X 4=60 | 11 X 6 X 8=528 |
# samples | 5 | 13 | |
** MAII score | log2(5/60*10)=-0.263034405833794 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(13/528*10)=-2.02202630633 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: FAM98C [Title/Abstract] AND SPINT2 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint | FAM98C(38894334)-SPINT2(38774267), # 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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | SPINT2 | GO:0022408 | negative regulation of cell-cell adhesion | 19592578 |
Tgene | SPINT2 | GO:2000146 | negative regulation of cell motility | 19592578 |
![]() * 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 | OV | TCGA-61-2094-01A | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
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Fusion Gene ORF analysis for FAM98C-SPINT2 |
![]() * 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 |
3UTR-3CDS | ENST00000585954 | ENST00000301244 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
3UTR-5UTR | ENST00000585954 | ENST00000587090 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
3UTR-intron | ENST00000585954 | ENST00000454580 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
5CDS-5UTR | ENST00000252530 | ENST00000587090 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
5CDS-5UTR | ENST00000343358 | ENST00000587090 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
5CDS-5UTR | ENST00000588262 | ENST00000587090 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
5CDS-intron | ENST00000252530 | ENST00000454580 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
5CDS-intron | ENST00000343358 | ENST00000454580 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
5CDS-intron | ENST00000588262 | ENST00000454580 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
In-frame | ENST00000252530 | ENST00000301244 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
In-frame | ENST00000343358 | ENST00000301244 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
In-frame | ENST00000588262 | ENST00000301244 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + |
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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) |
ENST00000588262 | FAM98C | chr19 | 38894334 | + | ENST00000301244 | SPINT2 | chr19 | 38774267 | + | 1629 | 368 | 19 | 1020 | 333 |
ENST00000252530 | FAM98C | chr19 | 38894334 | + | ENST00000301244 | SPINT2 | chr19 | 38774267 | + | 1629 | 368 | 19 | 1020 | 333 |
ENST00000343358 | FAM98C | chr19 | 38894334 | + | ENST00000301244 | SPINT2 | chr19 | 38774267 | + | 1610 | 349 | 0 | 1001 | 333 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000588262 | ENST00000301244 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + | 0.00210886 | 0.9978911 |
ENST00000252530 | ENST00000301244 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + | 0.00210886 | 0.9978911 |
ENST00000343358 | ENST00000301244 | FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774267 | + | 0.002113705 | 0.99788624 |
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Fusion Genomic Features for FAM98C-SPINT2 |
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Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | 1-p | p (fusion gene breakpoint) |
FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774266 | + | 3.61E-09 | 1 |
FAM98C | chr19 | 38894334 | + | SPINT2 | chr19 | 38774266 | + | 3.61E-09 | 1 |
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Fusion Protein Features for FAM98C-SPINT2 |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr19:38894334/chr19:38774267) - 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 |
FAM98C | . |
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 |
Tgene | SPINT2 | chr19:38894334 | chr19:38774267 | ENST00000301244 | 0 | 7 | 219_252 | 35 | 253.0 | Topological domain | Cytoplasmic | |
Tgene | SPINT2 | chr19:38894334 | chr19:38774267 | ENST00000454580 | 0 | 6 | 219_252 | 0 | 196.0 | Topological domain | Cytoplasmic | |
Tgene | SPINT2 | chr19:38894334 | chr19:38774267 | ENST00000454580 | 0 | 6 | 28_197 | 0 | 196.0 | Topological domain | Extracellular | |
Tgene | SPINT2 | chr19:38894334 | chr19:38774267 | ENST00000301244 | 0 | 7 | 198_218 | 35 | 253.0 | Transmembrane | Helical | |
Tgene | SPINT2 | chr19:38894334 | chr19:38774267 | ENST00000454580 | 0 | 6 | 198_218 | 0 | 196.0 | Transmembrane | Helical |
- 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 |
Tgene | SPINT2 | chr19:38894334 | chr19:38774267 | ENST00000301244 | 0 | 7 | 28_197 | 35 | 253.0 | Topological domain | Extracellular |
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Fusion Gene Sequence for FAM98C-SPINT2 |
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>29295_29295_1_FAM98C-SPINT2_FAM98C_chr19_38894334_ENST00000252530_SPINT2_chr19_38774267_ENST00000301244_length(transcript)=1629nt_BP=368nt GCGCCGAGACCACACTTTCATGGAGGCGGTGAAGGCGGAAGCGTGGGAGGGGGCCGCGGTGGCCCAGGACCTGCTGGCTCTGGGGTATGG AGGTGTCCCGGGGGCGGCGTCGCGGGGCGCCTCATGCCCAGACTTCAGGGGGCTGTGCGTGCGGCTGGCGGCGGAGCTGGCGACGCTGGG CGCCCTCGAGCAGCAGCGAGAGGCGGGCGCGGAGGTGCTGAGCGCCGGCGACGGCCCTGGCGCGGAGGAGGACTTTCTGCGGCAGCTCGG CAGCCTGCTGCGGGAGCTGCACTGCCCGGATCGCGCGCTCTGCGGCGGGGATGGCGCGGCTGCGCTTCGGGAACCCGGTGCCGGACTGCG CCTGCTGCACTTCTGCCTGGTGTCGAAGGTGGTGGGCAGATGCCGGGCCTCCATGCCTAGGTGGTGGTACAATGTCACTGACGGATCCTG CCAGCTGTTTGTGTATGGGGGCTGTGACGGAAACAGCAATAATTACCTGACCAAGGAGGAGTGCCTCAAGAAATGTGCCACTGTCACAGA GAATGCCACGGGTGACCTGGCCACCAGCAGGAATGCAGCGGATTCCTCTGTCCCAAGTGCTCCCAGAAGGCAGGATTCTGAAGACCACTC CAGCGATATGTTCAACTATGAAGAATACTGCACCGCCAACGCAGTCACTGGGCCTTGCCGTGCATCCTTCCCACGCTGGTACTTTGACGT GGAGAGGAACTCCTGCAATAACTTCATCTATGGAGGCTGCCGGGGCAATAAGAACAGCTACCGCTCTGAGGAGGCCTGCATGCTCCGCTG CTTCCGCCAGCAGGAGAATCCTCCCCTGCCCCTTGGCTCAAAGGTGGTGGTTCTGGCGGGGCTGTTCGTGATGGTGTTGATCCTCTTCCT GGGAGCCTCCATGGTCTACCTGATCCGGGTGGCACGGAGGAACCAGGAGCGTGCCCTGCGCACCGTCTGGAGCTCCGGAGATGACAAGGA GCAGCTGGTGAAGAACACATATGTCCTGTGACCGCCCTGTCGCCAAGAGGACTGGGGAAGGGAGGGGAGACTATGTGTGAGCTTTTTTTA AATAGAGGGATTGACTCGGATTTGAGTGATCATTAGGGCTGAGGTCTGTTTCTCTGGGAGGTAGGACGGCTGCTTCCTGGTCTGGCAGGG ATGGGTTTGCTTTGGAAATCCTCTAGGAGGCTCCTCCTCGCATGGCCTGCAGTCTGGCAGCAGCCCCGAGTTGTTTCCTCGCTGATCGAT TTCTTTCCTCCAGGTAGAGTTTTCTTTGCTTATGTTGAATTCCATTGCCTCTTTTCTCATCACAGAAGTGATGTTGGAATCGTTTCTTTT GTTTGTCTGATTTATGGTTTTTTTAAGTATAAACAAAAGTTTTTTATTAGCATTCTGAAAGAAGGAAAGTAAAATGTACAAGTTTAATAA AAAGGGGCCTTCCCCTTTAGAATAAATTTCAGCATGTGCTTTCTTTATGGGAGTCCTAATTTCAACCCTACCAAAATGATCACAAGACAC TATCTGAGGTGTCCCATTCTAGAAATAGACCCCTCAAAATAGCGTCTTTCAGATCTTTTTGAATGAATCCACAAGATGAAATAAATGTCC TATTACTGA >29295_29295_1_FAM98C-SPINT2_FAM98C_chr19_38894334_ENST00000252530_SPINT2_chr19_38774267_ENST00000301244_length(amino acids)=333AA_BP=112 MEAVKAEAWEGAAVAQDLLALGYGGVPGAASRGASCPDFRGLCVRLAAELATLGALEQQREAGAEVLSAGDGPGAEEDFLRQLGSLLREL HCPDRALCGGDGAAALREPGAGLRLLHFCLVSKVVGRCRASMPRWWYNVTDGSCQLFVYGGCDGNSNNYLTKEECLKKCATVTENATGDL ATSRNAADSSVPSAPRRQDSEDHSSDMFNYEEYCTANAVTGPCRASFPRWYFDVERNSCNNFIYGGCRGNKNSYRSEEACMLRCFRQQEN PPLPLGSKVVVLAGLFVMVLILFLGASMVYLIRVARRNQERALRTVWSSGDDKEQLVKNTYVL -------------------------------------------------------------- >29295_29295_2_FAM98C-SPINT2_FAM98C_chr19_38894334_ENST00000343358_SPINT2_chr19_38774267_ENST00000301244_length(transcript)=1610nt_BP=349nt ATGGAGGCGGTGAAGGCGGAAGCGTGGGAGGGGGCCGCGGTGGCCCAGGACCTGCTGGCTCTGGGGTATGGAGGTGTCCCGGGGGCGGCG TCGCGGGGCGCCTCATGCCCAGACTTCAGGGGGCTGTGCGTGCGGCTGGCGGCGGAGCTGGCGACGCTGGGCGCCCTCGAGCAGCAGCGA GAGGCGGGCGCGGAGGTGCTGAGCGCCGGCGACGGCCCTGGCGCGGAGGAGGACTTTCTGCGGCAGCTCGGCAGCCTGCTGCGGGAGCTG CACTGCCCGGATCGCGCGCTCTGCGGCGGGGATGGCGCGGCTGCGCTTCGGGAACCCGGTGCCGGACTGCGCCTGCTGCACTTCTGCCTG GTGTCGAAGGTGGTGGGCAGATGCCGGGCCTCCATGCCTAGGTGGTGGTACAATGTCACTGACGGATCCTGCCAGCTGTTTGTGTATGGG GGCTGTGACGGAAACAGCAATAATTACCTGACCAAGGAGGAGTGCCTCAAGAAATGTGCCACTGTCACAGAGAATGCCACGGGTGACCTG GCCACCAGCAGGAATGCAGCGGATTCCTCTGTCCCAAGTGCTCCCAGAAGGCAGGATTCTGAAGACCACTCCAGCGATATGTTCAACTAT GAAGAATACTGCACCGCCAACGCAGTCACTGGGCCTTGCCGTGCATCCTTCCCACGCTGGTACTTTGACGTGGAGAGGAACTCCTGCAAT AACTTCATCTATGGAGGCTGCCGGGGCAATAAGAACAGCTACCGCTCTGAGGAGGCCTGCATGCTCCGCTGCTTCCGCCAGCAGGAGAAT CCTCCCCTGCCCCTTGGCTCAAAGGTGGTGGTTCTGGCGGGGCTGTTCGTGATGGTGTTGATCCTCTTCCTGGGAGCCTCCATGGTCTAC CTGATCCGGGTGGCACGGAGGAACCAGGAGCGTGCCCTGCGCACCGTCTGGAGCTCCGGAGATGACAAGGAGCAGCTGGTGAAGAACACA TATGTCCTGTGACCGCCCTGTCGCCAAGAGGACTGGGGAAGGGAGGGGAGACTATGTGTGAGCTTTTTTTAAATAGAGGGATTGACTCGG ATTTGAGTGATCATTAGGGCTGAGGTCTGTTTCTCTGGGAGGTAGGACGGCTGCTTCCTGGTCTGGCAGGGATGGGTTTGCTTTGGAAAT CCTCTAGGAGGCTCCTCCTCGCATGGCCTGCAGTCTGGCAGCAGCCCCGAGTTGTTTCCTCGCTGATCGATTTCTTTCCTCCAGGTAGAG TTTTCTTTGCTTATGTTGAATTCCATTGCCTCTTTTCTCATCACAGAAGTGATGTTGGAATCGTTTCTTTTGTTTGTCTGATTTATGGTT TTTTTAAGTATAAACAAAAGTTTTTTATTAGCATTCTGAAAGAAGGAAAGTAAAATGTACAAGTTTAATAAAAAGGGGCCTTCCCCTTTA GAATAAATTTCAGCATGTGCTTTCTTTATGGGAGTCCTAATTTCAACCCTACCAAAATGATCACAAGACACTATCTGAGGTGTCCCATTC TAGAAATAGACCCCTCAAAATAGCGTCTTTCAGATCTTTTTGAATGAATCCACAAGATGAAATAAATGTCCTATTACTGA >29295_29295_2_FAM98C-SPINT2_FAM98C_chr19_38894334_ENST00000343358_SPINT2_chr19_38774267_ENST00000301244_length(amino acids)=333AA_BP=112 MEAVKAEAWEGAAVAQDLLALGYGGVPGAASRGASCPDFRGLCVRLAAELATLGALEQQREAGAEVLSAGDGPGAEEDFLRQLGSLLREL HCPDRALCGGDGAAALREPGAGLRLLHFCLVSKVVGRCRASMPRWWYNVTDGSCQLFVYGGCDGNSNNYLTKEECLKKCATVTENATGDL ATSRNAADSSVPSAPRRQDSEDHSSDMFNYEEYCTANAVTGPCRASFPRWYFDVERNSCNNFIYGGCRGNKNSYRSEEACMLRCFRQQEN PPLPLGSKVVVLAGLFVMVLILFLGASMVYLIRVARRNQERALRTVWSSGDDKEQLVKNTYVL -------------------------------------------------------------- >29295_29295_3_FAM98C-SPINT2_FAM98C_chr19_38894334_ENST00000588262_SPINT2_chr19_38774267_ENST00000301244_length(transcript)=1629nt_BP=368nt GCGCCGAGACCACACTTTCATGGAGGCGGTGAAGGCGGAAGCGTGGGAGGGGGCCGCGGTGGCCCAGGACCTGCTGGCTCTGGGGTATGG AGGTGTCCCGGGGGCGGCGTCGCGGGGCGCCTCATGCCCAGACTTCAGGGGGCTGTGCGTGCGGCTGGCGGCGGAGCTGGCGACGCTGGG CGCCCTCGAGCAGCAGCGAGAGGCGGGCGCGGAGGTGCTGAGCGCCGGCGACGGCCCTGGCGCGGAGGAGGACTTTCTGCGGCAGCTCGG CAGCCTGCTGCGGGAGCTGCACTGCCCGGATCGCGCGCTCTGCGGCGGGGATGGCGCGGCTGCGCTTCGGGAACCCGGTGCCGGACTGCG CCTGCTGCACTTCTGCCTGGTGTCGAAGGTGGTGGGCAGATGCCGGGCCTCCATGCCTAGGTGGTGGTACAATGTCACTGACGGATCCTG CCAGCTGTTTGTGTATGGGGGCTGTGACGGAAACAGCAATAATTACCTGACCAAGGAGGAGTGCCTCAAGAAATGTGCCACTGTCACAGA GAATGCCACGGGTGACCTGGCCACCAGCAGGAATGCAGCGGATTCCTCTGTCCCAAGTGCTCCCAGAAGGCAGGATTCTGAAGACCACTC CAGCGATATGTTCAACTATGAAGAATACTGCACCGCCAACGCAGTCACTGGGCCTTGCCGTGCATCCTTCCCACGCTGGTACTTTGACGT GGAGAGGAACTCCTGCAATAACTTCATCTATGGAGGCTGCCGGGGCAATAAGAACAGCTACCGCTCTGAGGAGGCCTGCATGCTCCGCTG CTTCCGCCAGCAGGAGAATCCTCCCCTGCCCCTTGGCTCAAAGGTGGTGGTTCTGGCGGGGCTGTTCGTGATGGTGTTGATCCTCTTCCT GGGAGCCTCCATGGTCTACCTGATCCGGGTGGCACGGAGGAACCAGGAGCGTGCCCTGCGCACCGTCTGGAGCTCCGGAGATGACAAGGA GCAGCTGGTGAAGAACACATATGTCCTGTGACCGCCCTGTCGCCAAGAGGACTGGGGAAGGGAGGGGAGACTATGTGTGAGCTTTTTTTA AATAGAGGGATTGACTCGGATTTGAGTGATCATTAGGGCTGAGGTCTGTTTCTCTGGGAGGTAGGACGGCTGCTTCCTGGTCTGGCAGGG ATGGGTTTGCTTTGGAAATCCTCTAGGAGGCTCCTCCTCGCATGGCCTGCAGTCTGGCAGCAGCCCCGAGTTGTTTCCTCGCTGATCGAT TTCTTTCCTCCAGGTAGAGTTTTCTTTGCTTATGTTGAATTCCATTGCCTCTTTTCTCATCACAGAAGTGATGTTGGAATCGTTTCTTTT GTTTGTCTGATTTATGGTTTTTTTAAGTATAAACAAAAGTTTTTTATTAGCATTCTGAAAGAAGGAAAGTAAAATGTACAAGTTTAATAA AAAGGGGCCTTCCCCTTTAGAATAAATTTCAGCATGTGCTTTCTTTATGGGAGTCCTAATTTCAACCCTACCAAAATGATCACAAGACAC TATCTGAGGTGTCCCATTCTAGAAATAGACCCCTCAAAATAGCGTCTTTCAGATCTTTTTGAATGAATCCACAAGATGAAATAAATGTCC TATTACTGA >29295_29295_3_FAM98C-SPINT2_FAM98C_chr19_38894334_ENST00000588262_SPINT2_chr19_38774267_ENST00000301244_length(amino acids)=333AA_BP=112 MEAVKAEAWEGAAVAQDLLALGYGGVPGAASRGASCPDFRGLCVRLAAELATLGALEQQREAGAEVLSAGDGPGAEEDFLRQLGSLLREL HCPDRALCGGDGAAALREPGAGLRLLHFCLVSKVVGRCRASMPRWWYNVTDGSCQLFVYGGCDGNSNNYLTKEECLKKCATVTENATGDL ATSRNAADSSVPSAPRRQDSEDHSSDMFNYEEYCTANAVTGPCRASFPRWYFDVERNSCNNFIYGGCRGNKNSYRSEEACMLRCFRQQEN PPLPLGSKVVVLAGLFVMVLILFLGASMVYLIRVARRNQERALRTVWSSGDDKEQLVKNTYVL -------------------------------------------------------------- |
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Fusion Gene PPI Analysis for FAM98C-SPINT2 |
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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 FAM98C-SPINT2 |
![]() (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 FAM98C-SPINT2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | C0267663 | Congenital secretory diarrhea, sodium type (disorder) | 3 | CTD_human;GENOMICS_ENGLAND;ORPHANET;UNIPROT | |
Tgene | C0007097 | Carcinoma | 1 | CTD_human | |
Tgene | C0011999 | Diastematomyelia | 1 | CTD_human | |
Tgene | C0024667 | Animal Mammary Neoplasms | 1 | CTD_human | |
Tgene | C0024668 | Mammary Neoplasms, Experimental | 1 | CTD_human | |
Tgene | C0027794 | Neural Tube Defects | 1 | CTD_human | |
Tgene | C0027806 | Neurenteric Cyst | 1 | CTD_human | |
Tgene | C0032045 | Placenta Disorders | 1 | CTD_human | |
Tgene | C0080218 | Tethered Cord Syndrome | 1 | CTD_human | |
Tgene | C0152234 | Iniencephaly | 1 | CTD_human | |
Tgene | C0152426 | Craniorachischisis | 1 | CTD_human | |
Tgene | C0152427 | Polydactyly | 1 | GENOMICS_ENGLAND | |
Tgene | C0155299 | Coloboma of optic disc | 1 | GENOMICS_ENGLAND | |
Tgene | C0205696 | Anaplastic carcinoma | 1 | CTD_human | |
Tgene | C0205697 | Carcinoma, Spindle-Cell | 1 | CTD_human | |
Tgene | C0205698 | Undifferentiated carcinoma | 1 | CTD_human | |
Tgene | C0205699 | Carcinomatosis | 1 | CTD_human | |
Tgene | C0266453 | Exencephaly | 1 | CTD_human | |
Tgene | C0302246 | Hexadactyly | 1 | GENOMICS_ENGLAND | |
Tgene | C0344479 | Spinal Cord Myelodysplasia | 1 | CTD_human | |
Tgene | C0702169 | Acrania | 1 | CTD_human | |
Tgene | C1257925 | Mammary Carcinoma, Animal | 1 | CTD_human | |
Tgene | C4275062 | Intestinal epithelial dysplasia | 1 | GENOMICS_ENGLAND |