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Fusion gene ID: 12642 |
FusionGeneSummary for FAM168B_NDST1 |
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Fusion gene information | Fusion gene name: FAM168B_NDST1 | Fusion gene ID: 12642 | Hgene | Tgene | Gene symbol | FAM168B | NDST1 | Gene ID | 130074 | 3340 |
Gene name | family with sequence similarity 168 member B | N-deacetylase and N-sulfotransferase 1 | |
Synonyms | MANI | HSST|MRT46|NST1 | |
Cytomap | 2q21.1 | 5q33.1 | |
Type of gene | protein-coding | protein-coding | |
Description | myelin-associated neurite-outgrowth inhibitorprotein FAM168B | bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1HSNST 1N-Deacetylase-N-sulfotransferase 1N-HSST 1N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1N-deacetylase/N-sulfotransferase 1N-heparan sulfate sulfotransferase 1NDST-1[H | |
Modification date | 20180519 | 20180519 | |
UniProtAcc | A1KXE4 | P52848 | |
Ensembl transtripts involved in fusion gene | ENST00000409185, ENST00000389915, | ENST00000523767, ENST00000261797, ENST00000521752, | |
Fusion gene scores | * DoF score | 5 X 7 X 2=70 | 3 X 3 X 3=27 |
# samples | 7 | 3 | |
** MAII score | log2(7/70*10)=0 | log2(3/27*10)=0.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context | PubMed: FAM168B [Title/Abstract] AND NDST1 [Title/Abstract] AND fusion [Title/Abstract] | ||
Functional or gene categories assigned by FusionGDB annotation |
* 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 | NDST1 | GO:0015012 | heparan sulfate proteoglycan biosynthetic process | 9915799 |
Tgene | NDST1 | GO:0015014 | heparan sulfate proteoglycan biosynthetic process, polysaccharide chain biosynthetic process | 9915799 |
![]() (ChiTars (NAR, 2018), tumorfusions (NAR, 2018), Gao et al. (Cell, 2018)) * 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. |
Data type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChiTaRS3.1 | BU631743 | FAM168B | chr2 | 131810549 | + | NDST1 | chr5 | 149937419 | - |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * 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-intron | ENST00000409185 | ENST00000523767 | FAM168B | chr2 | 131810549 | + | NDST1 | chr5 | 149937419 | - |
intron-3UTR | ENST00000409185 | ENST00000261797 | FAM168B | chr2 | 131810549 | + | NDST1 | chr5 | 149937419 | - |
intron-intron | ENST00000409185 | ENST00000521752 | FAM168B | chr2 | 131810549 | + | NDST1 | chr5 | 149937419 | - |
intron-intron | ENST00000389915 | ENST00000523767 | FAM168B | chr2 | 131810549 | + | NDST1 | chr5 | 149937419 | - |
intron-3UTR | ENST00000389915 | ENST00000261797 | FAM168B | chr2 | 131810549 | + | NDST1 | chr5 | 149937419 | - |
intron-intron | ENST00000389915 | ENST00000521752 | FAM168B | chr2 | 131810549 | + | NDST1 | chr5 | 149937419 | - |
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FusionProtFeatures for FAM168B_NDST1 |
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Hgene | Tgene |
FAM168B | NDST1 |
Modulates neuronal axonal outgrowth by acting as anegative regulator of CDC42 and STAT3 and a positive regulator ofSTMN2. Positive regulator of CDC27 (By similarity). {ECO:0000250}. | Essential bifunctional enzyme that catalyzes both the N-deacetylation and the N-sulfation of glucosamine (GlcNAc) of theglycosaminoglycan in heparan sulfate. Modifies the GlcNAc-GlcAdisaccharide repeating sugar backbone to make N-sulfatedheparosan, a prerequisite substrate for later modifications inheparin biosynthesis (PubMed:10758005, PubMed:12634318). Plays arole in determining the extent and pattern of sulfation of heparansulfate. Compared to other NDST enzymes, its presence isabsolutely required. Participates in biosynthesis of heparansulfate that can ultimately serve as L-selectin ligands, therebyplaying a role in inflammatory response (PubMed:10758005,PubMed:12634318). Required for the exosomal release of SDCBP, CD63and syndecan (PubMed:22660413). {ECO:0000269|PubMed:10758005,ECO:0000269|PubMed:12634318, ECO:0000269|PubMed:22660413}. |
![]() * 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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FusionGeneSequence for FAM168B_NDST1 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
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FusionGenePPI for FAM168B_NDST1 |
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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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RelatedDrugs for FAM168B_NDST1 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for FAM168B_NDST1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | NDST1 | C0015393 | Eye Abnormalities | 1 | CTD_human |
Tgene | NDST1 | C0376634 | Craniofacial Abnormalities | 1 | CTD_human |
Tgene | NDST1 | C1955869 | Malformations of Cortical Development | 1 | CTD_human |
Tgene | NDST1 | C3714756 | Intellectual Disability | 1 | CTD_human;HPO |
Tgene | NDST1 | C4015283 | MENTAL RETARDATION, AUTOSOMAL RECESSIVE 46 | 1 | UNIPROT |