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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: 14027

FusionGeneSummary for FTH1_AVL9

check button Fusion gene summary
Fusion gene informationFusion gene name: FTH1_AVL9
Fusion gene ID: 14027
HgeneTgene
Gene symbol

FTH1

AVL9

Gene ID

2495

23080

Gene nameferritin heavy chain 1AVL9 cell migration associated
SynonymsFHC|FTH|FTHL6|HFE5|PIG15|PLIFKIAA0241
Cytomap

11q12.3

7p14.3

Type of geneprotein-codingprotein-coding
Descriptionferritin heavy chainapoferritincell proliferation-inducing gene 15 proteinferritin H subunitferritin, heavy polypeptide 1placenta immunoregulatory factorproliferation-inducing protein 15late secretory pathway protein AVL9 homologAVL9 homolog (S. cerevisiase)
Modification date2018052320180523
UniProtAcc

P02794

Q8NBF6

Ensembl transtripts involved in fusion geneENST00000529631, ENST00000529191, 
ENST00000273550, ENST00000526640, 
ENST00000532601, 
ENST00000404479, 
ENST00000318709, ENST00000459629, 
ENST00000409301, 
Fusion gene scores* DoF score6 X 6 X 1=368 X 9 X 3=216
# samples 69
** MAII scorelog2(6/36*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(9/216*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FTH1 [Title/Abstract] AND AVL9 [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
HgeneFTH1

GO:0006880

intracellular sequestering of iron ion

9924025

HgeneFTH1

GO:0048147

negative regulation of fibroblast proliferation

9924025

TgeneAVL9

GO:0016477

cell migration

22595670


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
ChiTaRS3.1BG527923FTH1chr11

61734981

-AVL9chr7

33102232

-
* 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
intron-intronENST00000529631ENST00000404479FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000529631ENST00000318709FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000529631ENST00000459629FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000529631ENST00000409301FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000529191ENST00000404479FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000529191ENST00000318709FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000529191ENST00000459629FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000529191ENST00000409301FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000273550ENST00000404479FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000273550ENST00000318709FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000273550ENST00000459629FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000273550ENST00000409301FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000526640ENST00000404479FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000526640ENST00000318709FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000526640ENST00000459629FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000526640ENST00000409301FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000532601ENST00000404479FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000532601ENST00000318709FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000532601ENST00000459629FTH1chr11

61734981

-AVL9chr7

33102232

-
intron-intronENST00000532601ENST00000409301FTH1chr11

61734981

-AVL9chr7

33102232

-

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FusionProtFeatures for FTH1_AVL9


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FTH1

P02794

AVL9

Q8NBF6

Stores iron in a soluble, non-toxic, readily availableform. Important for iron homeostasis. Has ferroxidase activity.Iron is taken up in the ferrous form and deposited as ferrichydroxides after oxidation. Also plays a role in delivery of ironto cells. Mediates iron uptake in capsule cells of the developingkidney (By similarity). {ECO:0000250}. Functions in cell migration.{ECO:0000269|PubMed:22595670}.

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 FTH1_AVL9


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 FTH1_AVL9


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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RelatedDrugs for FTH1_AVL9


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneFTH1P02794DB01592IronFerritin heavy chainsmall moleculeapproved

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RelatedDiseases for FTH1_AVL9


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFTH1C0011581Depressive disorder1CTD_human
HgeneFTH1C0011616Contact Dermatitis1CTD_human
HgeneFTH1C0017638Glioma1CTD_human
HgeneFTH1C0022548Keloid1CTD_human
HgeneFTH1C0027626Neoplasm Invasiveness1CTD_human
HgeneFTH1C0032927Precancerous Conditions1CTD_human
HgeneFTH1C0282193Iron Overload1CTD_human
HgeneFTH1C0345967Malignant mesothelioma1CTD_human
HgeneFTH1C0524851Neurodegenerative Disorders1CTD_human
TgeneAVL9C3495559Juvenile arthritis1CTD_human