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Fusion gene ID: 2779 |
FusionGeneSummary for ARMCX4_NSD1 |
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Fusion gene information | Fusion gene name: ARMCX4_NSD1 | Fusion gene ID: 2779 | Hgene | Tgene | Gene symbol | ARMCX4 | NSD1 | Gene ID | 100131755 | 64324 |
Gene name | armadillo repeat containing X-linked 4 | nuclear receptor binding SET domain protein 1 | |
Synonyms | CXorf35|GASP4 | ARA267|KMT3B|SOTOS|SOTOS1|STO | |
Cytomap | Xq22.1 | 5q35.3 | |
Type of gene | protein-coding | protein-coding | |
Description | armadillo repeat-containing X-linked protein 4armadillo repeat containing, X-linked 4 pseudogene | histone-lysine N-methyltransferase, H3 lysine-36 and H4 lysine-20 specificH3-K36-HMTaseH4-K20-HMTaseNR-binding SET domain-containing proteinandrogen receptor coactivator 267 kDa proteinandrogen receptor-associated coregulator 267androgen receptor-as | |
Modification date | 20180519 | 20180519 | |
UniProtAcc | Q5H9R4 | Q96L73 | |
Ensembl transtripts involved in fusion gene | ENST00000431677, ENST00000423738, | ENST00000354179, ENST00000439151, ENST00000347982, ENST00000361032, ENST00000511258, | |
Fusion gene scores | * DoF score | 2 X 2 X 2=8 | 7 X 7 X 4=196 |
# samples | 2 | 10 | |
** MAII score | log2(2/8*10)=1.32192809488736 | log2(10/196*10)=-0.970853654340483 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ARMCX4 [Title/Abstract] AND NSD1 [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 | NSD1 | GO:0045893 | positive regulation of transcription, DNA-templated | 11509567 |
![]() (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 | BE173509 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
* 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 | ENST00000431677 | ENST00000354179 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
intron-intron | ENST00000431677 | ENST00000439151 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
intron-intron | ENST00000431677 | ENST00000347982 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
intron-intron | ENST00000431677 | ENST00000361032 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
intron-intron | ENST00000431677 | ENST00000511258 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
intron-intron | ENST00000423738 | ENST00000354179 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
intron-intron | ENST00000423738 | ENST00000439151 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
intron-intron | ENST00000423738 | ENST00000347982 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
intron-intron | ENST00000423738 | ENST00000361032 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
intron-intron | ENST00000423738 | ENST00000511258 | ARMCX4 | chrX | 100707798 | - | NSD1 | chr5 | 176569434 | + |
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FusionProtFeatures for ARMCX4_NSD1 |
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Hgene | Tgene |
ARMCX4 | NSD1 |
Histone methyltransferase. Preferentially methylates'Lys-36' of histone H3 and 'Lys-20' of histone H4 (in vitro).Transcriptional intermediary factor capable of both negatively orpositively influencing transcription, depending on the cellularcontext. {ECO:0000269|PubMed:21196496}. |
![]() * 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 ARMCX4_NSD1 |
![]() (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 ARMCX4_NSD1 |
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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 ARMCX4_NSD1 |
![]() (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 ARMCX4_NSD1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | NSD1 | C0175695 | Sotos' syndrome | 14 | CTD_human;ORPHANET;UNIPROT |
Tgene | NSD1 | C0004352 | Autistic Disorder | 1 | CTD_human |
Tgene | NSD1 | C0010606 | Adenoid Cystic Carcinoma | 1 | CTD_human |
Tgene | NSD1 | C0265210 | Weaver syndrome | 1 | CTD_human;ORPHANET |
Tgene | NSD1 | C3714756 | Intellectual Disability | 1 | CTD_human |