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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: 13302

FusionGeneSummary for FECH_FECH

check button Fusion gene summary
Fusion gene informationFusion gene name: FECH_FECH
Fusion gene ID: 13302
HgeneTgene
Gene symbol

FECH

FECH

Gene ID

2235

2235

Gene nameferrochelataseferrochelatase
SynonymsEPP|FCEEPP|FCE
Cytomap

18q21.31

18q21.31

Type of geneprotein-codingprotein-coding
Descriptionferrochelatase, mitochondrialheme synthaseheme synthetaseprotoheme ferro-lyaseprotoporphyriaferrochelatase, mitochondrialheme synthaseheme synthetaseprotoheme ferro-lyaseprotoporphyria
Modification date2018052320180523
UniProtAcc

P22830

P22830

Ensembl transtripts involved in fusion geneENST00000262093, ENST00000382873, 
ENST00000585699, 
ENST00000262093, 
ENST00000382873, ENST00000585699, 
Fusion gene scores* DoF score4 X 4 X 3=483 X 3 X 2=18
# samples 43
** MAII scorelog2(4/48*10)=-0.263034405833794
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: FECH [Title/Abstract] AND FECH [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
HgeneFECH

GO:0046501

protoporphyrinogen IX metabolic process

15123683

TgeneFECH

GO:0046501

protoporphyrinogen IX metabolic process

15123683


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
ChiTaRS3.1AW607390FECHchr18

55226434

-FECHchr18

55218563

+
* 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-3CDSENST00000262093ENST00000262093FECHchr18

55226434

-FECHchr18

55218563

+
intron-3CDSENST00000262093ENST00000382873FECHchr18

55226434

-FECHchr18

55218563

+
intron-intronENST00000262093ENST00000585699FECHchr18

55226434

-FECHchr18

55218563

+
intron-3CDSENST00000382873ENST00000262093FECHchr18

55226434

-FECHchr18

55218563

+
intron-3CDSENST00000382873ENST00000382873FECHchr18

55226434

-FECHchr18

55218563

+
intron-intronENST00000382873ENST00000585699FECHchr18

55226434

-FECHchr18

55218563

+
intron-3CDSENST00000585699ENST00000262093FECHchr18

55226434

-FECHchr18

55218563

+
intron-3CDSENST00000585699ENST00000382873FECHchr18

55226434

-FECHchr18

55218563

+
intron-intronENST00000585699ENST00000585699FECHchr18

55226434

-FECHchr18

55218563

+

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FusionProtFeatures for FECH_FECH


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

P22830

FECH

P22830

Catalyzes the ferrous insertion into protoporphyrin IX. Catalyzes the ferrous insertion into protoporphyrin IX.

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 FECH_FECH


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 FECH_FECH


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 FECH_FECH


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneFECHP22830DB02659Cholic AcidFerrochelatase, mitochondrialsmall moleculeapproved
TgeneFECHP22830DB02659Cholic AcidFerrochelatase, mitochondrialsmall moleculeapproved

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RelatedDiseases for FECH_FECH


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFECHC0162568Erythropoietic Protoporphyria17CTD_human;ORPHANET;UNIPROT
HgeneFECHC0005395Bile Duct Diseases1CTD_human
HgeneFECHC0016059Fibrosis1CTD_human
TgeneFECHC0162568Erythropoietic Protoporphyria17CTD_human;ORPHANET;UNIPROT
TgeneFECHC0005395Bile Duct Diseases1CTD_human
TgeneFECHC0016059Fibrosis1CTD_human