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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:C16orf58-ITGAM (FusionGDB2 ID:11057)

Fusion Gene Summary for C16orf58-ITGAM

check button Fusion gene summary
Fusion gene informationFusion gene name: C16orf58-ITGAM
Fusion gene ID: 11057
HgeneTgene
Gene symbol

C16orf58

ITGAM

Gene ID

64755

3684

Gene nameRUS family member 1integrin subunit alpha M
SynonymsC16orf58|RUSCD11B|CR3A|MAC-1|MAC1A|MO1A|SLEB6
Cytomap

16p11.2

16p11.2

Type of geneprotein-codingprotein-coding
DescriptionRUS1 family protein C16orf58RUS1 homologUPF0420 protein C16orf58root UVB sensitivityintegrin alpha-MCD11 antigen-like family member BCR-3 alpha chainantigen CD11b (p170)cell surface glycoprotein MAC-1 subunit alphacomplement component 3 receptor 3 subunitintegrin, alpha M (complement component 3 receptor 3 subunit)leukocyte adhesi
Modification date2020031320200313
UniProtAcc.

P11215

Ensembl transtripts involved in fusion geneENST00000570164, ENST00000327237, 
ENST00000567994, ENST00000430477, 
ENST00000287497, ENST00000544665, 
Fusion gene scores* DoF score4 X 4 X 2=324 X 5 X 4=80
# samples 45
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(5/80*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: C16orf58 [Title/Abstract] AND ITGAM [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointC16orf58(31500741)-ITGAM(31284735), # 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)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID

check buttonFusion gene breakpoints across C16orf58 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across ITGAM (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChimerDB4HNSCTCGA-CV-A465C16orf58chr16

31500741

-ITGAMchr16

31284735

+


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Fusion Gene ORF analysis for C16orf58-ITGAM

check button 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.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
intron-3CDSENST00000570164ENST00000287497C16orf58chr16

31500741

-ITGAMchr16

31284735

+
intron-3CDSENST00000570164ENST00000544665C16orf58chr16

31500741

-ITGAMchr16

31284735

+
intron-3CDSENST00000327237ENST00000287497C16orf58chr16

31500741

-ITGAMchr16

31284735

+
intron-3CDSENST00000327237ENST00000544665C16orf58chr16

31500741

-ITGAMchr16

31284735

+
intron-3CDSENST00000567994ENST00000287497C16orf58chr16

31500741

-ITGAMchr16

31284735

+
intron-3CDSENST00000567994ENST00000544665C16orf58chr16

31500741

-ITGAMchr16

31284735

+
intron-3CDSENST00000430477ENST00000287497C16orf58chr16

31500741

-ITGAMchr16

31284735

+
intron-3CDSENST00000430477ENST00000544665C16orf58chr16

31500741

-ITGAMchr16

31284735

+

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF 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.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for C16orf58-ITGAM


check buttonFusionAI 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.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution 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.

check buttonDistribution 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 C16orf58-ITGAM


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
.ITGAM

P11215

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.FUNCTION: Integrin ITGAM/ITGB2 is implicated in various adhesive interactions of monocytes, macrophages and granulocytes as well as in mediating the uptake of complement-coated particles and pathogens (PubMed:9558116, PubMed:20008295). It is identical with CR-3, the receptor for the iC3b fragment of the third complement component. It probably recognizes the R-G-D peptide in C3b. Integrin ITGAM/ITGB2 is also a receptor for fibrinogen, factor X and ICAM1. It recognizes P1 and P2 peptides of fibrinogen gamma chain. Regulates neutrophil migration (PubMed:28807980). In association with beta subunit ITGB2/CD18, required for CD177-PRTN3-mediated activation of TNF primed neutrophils (PubMed:21193407). May regulate phagocytosis-induced apoptosis in extravasated neutrophils (By similarity). May play a role in mast cell development (By similarity). Required with TYROBP/DAP12 in microglia to control production of microglial superoxide ions which promote the neuronal apoptosis that occurs during brain development (By similarity). {ECO:0000250|UniProtKB:P05555, ECO:0000269|PubMed:20008295, ECO:0000269|PubMed:21193407, ECO:0000269|PubMed:28807980, ECO:0000269|PubMed:9558116, ECO:0000305}.

check buttonRetention 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

download page


* 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.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for C16orf58-ITGAM


check button 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.

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Fusion Gene PPI Analysis for C16orf58-ITGAM


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for C16orf58-ITGAM


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for C16orf58-ITGAM


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneITGAMC0024141Lupus Erythematosus, Systemic5CTD_human;ORPHANET
TgeneITGAMC0242380Libman-Sacks Disease2CTD_human
TgeneITGAMC0005586Bipolar Disorder1PSYGENET
TgeneITGAMC0020456Hyperglycemia1CTD_human
TgeneITGAMC0020459Hyperinsulinism1CTD_human
TgeneITGAMC0020877Ileitis1CTD_human
TgeneITGAMC0021655Insulin Resistance1CTD_human
TgeneITGAMC0023487Acute Promyelocytic Leukemia1CTD_human
TgeneITGAMC0028754Obesity1CTD_human
TgeneITGAMC0036341Schizophrenia1PSYGENET
TgeneITGAMC0162820Dermatitis, Allergic Contact1CTD_human
TgeneITGAMC0752332Lupus Vasculitis, Central Nervous System1CTD_human
TgeneITGAMC0752334Lupus Meningoencephalitis1CTD_human
TgeneITGAMC0752335Neuropsychiatric Systemic Lupus Erythematosus1CTD_human
TgeneITGAMC0920563Insulin Sensitivity1CTD_human
TgeneITGAMC1257963Endogenous Hyperinsulinism1CTD_human
TgeneITGAMC1257964Exogenous Hyperinsulinism1CTD_human
TgeneITGAMC1257965Compensatory Hyperinsulinemia1CTD_human
TgeneITGAMC1855520Hyperglycemia, Postprandial1CTD_human