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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 37877

FusionGeneSummary for TF_HMGCS2

check button Fusion gene summary
Fusion gene informationFusion gene name: TF_HMGCS2
Fusion gene ID: 37877
HgeneTgene
Gene symbol

TF

HMGCS2

Gene ID

7018

3158

Gene nametransferrin3-hydroxy-3-methylglutaryl-CoA synthase 2
SynonymsHEL-S-71p|PRO1557|PRO2086|TFQTL1-
Cytomap

3q22.1

1p12

Type of geneprotein-codingprotein-coding
Descriptionserotransferrinbeta-1 metal-binding globulinepididymis secretory sperm binding protein Li 71psiderophilinhydroxymethylglutaryl-CoA synthase, mitochondrial3-hydroxy-3-methylglutaryl-CoA synthase 2 (mitochondrial)3-hydroxy-3-methylglutaryl-Coenzyme A synthase 2 (mitochondrial)HMG-CoA synthasetesticular tissue protein Li 88
Modification date2018052320180523
UniProtAcc

P02787

P54868

Ensembl transtripts involved in fusion geneENST00000402696, ENST00000264998, 
ENST00000475382, 
ENST00000369406, 
ENST00000544913, ENST00000476640, 
Fusion gene scores* DoF score13 X 9 X 2=2343 X 3 X 2=18
# samples 173
** MAII scorelog2(17/234*10)=-0.460973783445703
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: TF [Title/Abstract] AND HMGCS2 [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)

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

GO:0048260

positive regulation of receptor-mediated endocytosis

12704209


check button Fusion gene information from three resources
(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 typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
TCGALDLIHCTCGA-DD-A73C-01ATFchr3

133473515

+HMGCS2chr1

120293531

-
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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
Frame-shiftENST00000402696ENST00000369406TFchr3

133473515

+HMGCS2chr1

120293531

-
Frame-shiftENST00000402696ENST00000544913TFchr3

133473515

+HMGCS2chr1

120293531

-
5CDS-intronENST00000402696ENST00000476640TFchr3

133473515

+HMGCS2chr1

120293531

-
Frame-shiftENST00000264998ENST00000369406TFchr3

133473515

+HMGCS2chr1

120293531

-
Frame-shiftENST00000264998ENST00000544913TFchr3

133473515

+HMGCS2chr1

120293531

-
5CDS-intronENST00000264998ENST00000476640TFchr3

133473515

+HMGCS2chr1

120293531

-
intron-3CDSENST00000475382ENST00000369406TFchr3

133473515

+HMGCS2chr1

120293531

-
intron-3CDSENST00000475382ENST00000544913TFchr3

133473515

+HMGCS2chr1

120293531

-
intron-intronENST00000475382ENST00000476640TFchr3

133473515

+HMGCS2chr1

120293531

-

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FusionProtFeatures for TF_HMGCS2


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

P02787

HMGCS2

P54868

Transferrins are iron binding transport proteins whichcan bind two Fe(3+) ions in association with the binding of ananion, usually bicarbonate. It is responsible for the transport ofiron from sites of absorption and heme degradation to those ofstorage and utilization. Serum transferrin may also have a furtherrole in stimulating cell proliferation. This enzyme condenses acetyl-CoA with acetoacetyl-CoA toform HMG-CoA, which is the substrate for HMG-CoA reductase.

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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FusionGeneSequence for TF_HMGCS2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(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 TF_HMGCS2


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
TFFNBP1, TUBB3, IGF1, IGF2, IGFBP3, CALR, CANX, TFRC, TFR2, MIS12, GRB2, PSMA3, RAB5A, TYRP1, ESR1, VKORC1, MYC, FN1, LAMC3, TIMELESS, SMAD3, CA8, GDPD1, DDX19B, GLRA2, MATN3, STPG2, SH2D4A, SLC38A6, SYT17, UTP3, EDIL3, ALDH2, SNX27, DDX31, MAPK6, CCDC82, C3, IGHG4HMGCS2YWHAQ, APP, HSD17B10, NFATC1, PDE4DIP


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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RelatedDrugs for TF_HMGCS2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneTFP02787DB00515CisplatinSerotransferrinsmall moleculeapproved
HgeneTFP02787DB01592IronSerotransferrinsmall moleculeapproved
HgeneTFP02787DB01370AluminiumSerotransferrinsmall moleculeapproved|investigational
HgeneTFP02787DB01593ZincSerotransferrinsmall moleculeapproved|investigational

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RelatedDiseases for TF_HMGCS2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTFC0036341Schizophrenia3PSYGENET
HgeneTFC0521802Congenital atransferrinemia3CTD_human;HPO;ORPHANET;UNIPROT
HgeneTFC0001973Alcoholic Intoxication, Chronic2CTD_human
HgeneTFC0002395Alzheimer's Disease2CTD_human
HgeneTFC0015695Fatty Liver2CTD_human
HgeneTFC0024667Animal Mammary Neoplasms2CTD_human
HgeneTFC0024668Mammary Neoplasms, Experimental2CTD_human
HgeneTFC0004352Autistic Disorder1CTD_human
HgeneTFC0013502Echinococcosis1CTD_human
HgeneTFC0019158Hepatitis1CTD_human
HgeneTFC0021368Inflammation1CTD_human
HgeneTFC0027626Neoplasm Invasiveness1CTD_human
HgeneTFC0027726Nephrotic Syndrome1CTD_human
HgeneTFC0028754Obesity1CTD_human
HgeneTFC0030524Paratuberculosis1CTD_human
HgeneTFC0035258Restless Legs Syndrome1CTD_human
HgeneTFC0036337Schizoaffective Disorder1PSYGENET
HgeneTFC0152013Adenocarcinoma of lung (disorder)1CTD_human
HgeneTFC0271901Microcytic hypochromic anemia (disorder)1CTD_human
HgeneTFC0282193Iron Overload1CTD_human
HgeneTFC0345967Malignant mesothelioma1CTD_human
HgeneTFC4277682Chemical and Drug Induced Liver Injury1CTD_human
TgeneHMGCS2C27515323-Hydroxy-3-Methylglutaryl-CoA Synthase 2 Deficiency3CTD_human;ORPHANET;UNIPROT
TgeneHMGCS2C0009375Colonic Neoplasms1CTD_human
TgeneHMGCS2C0151744Myocardial Ischemia1CTD_human