FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

Fusion Gene Summary

leaf

Fusion Gene ORF analysis

leaf

Fusion Genomic Features

leaf

Fusion Protein Features

leaf

Fusion Gene Sequence

leaf

Fusion Gene PPI analysis

leaf

Related Drugs

leaf

Related Diseases

Fusion gene:GNAZ-MIF (FusionGDB2 ID:33539)

Fusion Gene Summary for GNAZ-MIF

check button Fusion gene summary
Fusion gene informationFusion gene name: GNAZ-MIF
Fusion gene ID: 33539
HgeneTgene
Gene symbol

GNAZ

MIF

Gene ID

2781

6280

Gene nameG protein subunit alpha zS100 calcium binding protein A9
Synonymsgz-alpha60B8AG|CAGB|CFAG|CGLB|L1AG|LIAG|MAC387|MIF|MRP14|NIF|P14
Cytomap

22q11.22-q11.23

1q21.3

Type of geneprotein-codingprotein-coding
Descriptionguanine nucleotide-binding protein G(z) subunit alphag(x) alpha chainguanine nucleotide binding protein (G protein), alpha z polypeptidetransducin alphaprotein S100-A9MRP-14calgranulin Bcalprotectin L1H subunitleukocyte L1 complex heavy chainmigration inhibitory factor-related protein 14
Modification date2020031320200329
UniProtAcc.

A9UHW6

Ensembl transtripts involved in fusion geneENST00000248996, ENST00000492538, 
ENST00000215754, 
Fusion gene scores* DoF score3 X 2 X 3=186 X 4 X 5=120
# samples 410
** MAII scorelog2(4/18*10)=1.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(10/120*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: GNAZ [Title/Abstract] AND MIF [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointGNAZ(23412756)-MIF(24236959), # samples:2
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
TgeneMIF

GO:0002523

leukocyte migration involved in inflammatory response

12626582

TgeneMIF

GO:0006914

autophagy

19935772

TgeneMIF

GO:0006919

activation of cysteine-type endopeptidase activity involved in apoptotic process

19935772

TgeneMIF

GO:0030593

neutrophil chemotaxis

12626582

TgeneMIF

GO:0035606

peptidyl-cysteine S-trans-nitrosylation

25417112

TgeneMIF

GO:0035821

modification of morphology or physiology of other organism

12874352

TgeneMIF

GO:0050729

positive regulation of inflammatory response

12626582

TgeneMIF

GO:0061844

antimicrobial humoral immune response mediated by antimicrobial peptide

12874352

TgeneMIF

GO:0070488

neutrophil aggregation

12626582

TgeneMIF

GO:2001244

positive regulation of intrinsic apoptotic signaling pathway

19935772


check buttonFusion gene breakpoints across GNAZ (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 MIF (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
ChimerDB4OVTCGA-24-2019-01AGNAZchr22

23412756

+MIFchr22

24236959

+
ChimerDB4OVTCGA-24-2019GNAZchr22

23412756

+MIFchr22

24236958

+
ChimerDB4OVTCGA-24-2019-01AGNAZchr22

23412756

+MIFchr22

24236959

+


Top

Fusion Gene ORF analysis for GNAZ-MIF

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
5UTR-3CDSENST00000248996ENST00000215754GNAZchr22

23412756

+MIFchr22

24236959

+
intron-3CDSENST00000492538ENST00000215754GNAZchr22

23412756

+MIFchr22

24236959

+
5UTR-3CDSENST00000248996ENST00000215754GNAZchr22

23412756

+MIFchr22

24236958

+
intron-3CDSENST00000492538ENST00000215754GNAZchr22

23412756

+MIFchr22

24236958

+

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

Top

Fusion Genomic Features for GNAZ-MIF


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)
GNAZchr2223412756+MIFchr2224236958+0.0003212430.99967873
GNAZchr2223412756+MIFchr2224236958+0.0003212430.99967873
GNAZchr2223412756+MIFchr2224236958+0.0003212430.99967873
GNAZchr2223412756+MIFchr2224236958+0.0003212430.99967873

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.

Top

Fusion Protein Features for GNAZ-MIF


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
.MIF

A9UHW6

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: Functions in replication-dependent translation of histone mRNAs which differ from other eukaryotic mRNAs in that they do not end with a poly-A tail but a stem-loop. May participate in circularizing those mRNAs specifically enhancing their translation. {ECO:0000269|PubMed:18025107}.

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


Top

Fusion Gene Sequence for GNAZ-MIF


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.

Top

Fusion Gene PPI Analysis for GNAZ-MIF


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


Top

Related Drugs for GNAZ-MIF


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

Top

Related Diseases for GNAZ-MIF


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneGNAZC2239176Liver carcinoma1CTD_human
TgeneMIFC0003469Anxiety Disorders1CTD_human
TgeneMIFC0003873Rheumatoid Arthritis1CTD_human
TgeneMIFC0004352Autistic Disorder1CTD_human
TgeneMIFC0006142Malignant neoplasm of breast1CTD_human
TgeneMIFC0007097Carcinoma1CTD_human
TgeneMIFC0009319Colitis1CTD_human
TgeneMIFC0011573Endogenous depression1CTD_human
TgeneMIFC0011581Depressive disorder1CTD_human
TgeneMIFC0014518Toxic Epidermal Necrolysis1CTD_human
TgeneMIFC0021368Inflammation1CTD_human
TgeneMIFC0022548Keloid1CTD_human
TgeneMIFC0024667Animal Mammary Neoplasms1CTD_human
TgeneMIFC0024668Mammary Neoplasms, Experimental1CTD_human
TgeneMIFC0025193Melancholia1CTD_human
TgeneMIFC0025261Memory Disorders1CTD_human
TgeneMIFC0033578Prostatic Neoplasms1CTD_human
TgeneMIFC0034189Pyemia1CTD_human
TgeneMIFC0036690Septicemia1CTD_human
TgeneMIFC0038325Stevens-Johnson Syndrome1CTD_human
TgeneMIFC0041696Unipolar Depression1CTD_human
TgeneMIFC0086133Depressive Syndrome1CTD_human
TgeneMIFC0205696Anaplastic carcinoma1CTD_human
TgeneMIFC0205697Carcinoma, Spindle-Cell1CTD_human
TgeneMIFC0205698Undifferentiated carcinoma1CTD_human
TgeneMIFC0205699Carcinomatosis1CTD_human
TgeneMIFC0233794Memory impairment1CTD_human
TgeneMIFC0243026Sepsis1CTD_human
TgeneMIFC0282126Depression, Neurotic1CTD_human
TgeneMIFC0345967Malignant mesothelioma1CTD_human
TgeneMIFC0376280Anxiety States, Neurotic1CTD_human
TgeneMIFC0376358Malignant neoplasm of prostate1CTD_human
TgeneMIFC0678222Breast Carcinoma1CTD_human
TgeneMIFC0751292Age-Related Memory Disorders1CTD_human
TgeneMIFC0751293Memory Disorder, Semantic1CTD_human
TgeneMIFC0751294Memory Disorder, Spatial1CTD_human
TgeneMIFC0751295Memory Loss1CTD_human
TgeneMIFC1257925Mammary Carcinoma, Animal1CTD_human
TgeneMIFC1257931Mammary Neoplasms, Human1CTD_human
TgeneMIFC1274933Drug-Induced Stevens Johnson Syndrome1CTD_human
TgeneMIFC1279420Anxiety neurosis (finding)1CTD_human
TgeneMIFC1458155Mammary Neoplasms1CTD_human
TgeneMIFC1719672Severe Sepsis1CTD_human
TgeneMIFC3658301Mycoplasma-Induced Stevens-Johnson Syndrome1CTD_human
TgeneMIFC3658302Stevens-Johnson Syndrome Toxic Epidermal Necrolysis Spectrum1CTD_human
TgeneMIFC4704874Mammary Carcinoma, Human1CTD_human