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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: 4734

FusionGeneSummary for C16orf62_C9

check button Fusion gene summary
Fusion gene informationFusion gene name: C16orf62_C9
Fusion gene ID: 4734
HgeneTgene
Gene symbol

C16orf62

C9

Gene ID

1645

Gene namealdo-keto reductase family 1 member C1
Synonyms2-ALPHA-HSD|20-ALPHA-HSD|C9|DD1|DD1/DD2|DDH|DDH1|H-37|HAKRC|HBAB|MBAB
Cytomap

10p15.1

Type of geneprotein-coding
Descriptionaldo-keto reductase family 1 member C120 alpha-hydroxysteroid dehydrogenasealdo-keto reductase Cchlordecone reductase homolog HAKRCdihydrodiol dehydrogenase 1dihydrodiol dehydrogenase 1/2dihydrodiol dehydrogenase 1; 20-alpha (3-alpha)-hydroxysteroid
Modification date20180523
UniProtAcc

Q7Z3J2

P02748

Ensembl transtripts involved in fusion geneENST00000438132, ENST00000542263, 
ENST00000417362, ENST00000251143, 
ENST00000543152, ENST00000448695, 
ENST00000544275, ENST00000538853, 
ENST00000263408, ENST00000509186, 
Fusion gene scores* DoF score5 X 5 X 4=1005 X 4 X 3=60
# samples 55
** MAII scorelog2(5/100*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: C16orf62 [Title/Abstract] AND C9 [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
TgeneC9

GO:0007586

digestion

8486699

TgeneC9

GO:0008206

bile acid metabolic process

8486699

TgeneC9

GO:0030855

epithelial cell differentiation

21492153

TgeneC9

GO:0042448

progesterone metabolic process

21232532

TgeneC9

GO:0042574

retinal metabolic process

21851338

TgeneC9

GO:0051260

protein homooligomerization

8486699

TgeneC9

GO:0055114

oxidation-reduction process

8486699|19442656|21232532

TgeneC9

GO:0071395

cellular response to jasmonic acid stimulus

19487289


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-G3-A5SM-01AC16orf62chr16

19613045

+C9chr5

39285335

-
* 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-shiftENST00000438132ENST00000263408C16orf62chr16

19613045

+C9chr5

39285335

-
5CDS-intronENST00000438132ENST00000509186C16orf62chr16

19613045

+C9chr5

39285335

-
Frame-shiftENST00000542263ENST00000263408C16orf62chr16

19613045

+C9chr5

39285335

-
5CDS-intronENST00000542263ENST00000509186C16orf62chr16

19613045

+C9chr5

39285335

-
Frame-shiftENST00000417362ENST00000263408C16orf62chr16

19613045

+C9chr5

39285335

-
5CDS-intronENST00000417362ENST00000509186C16orf62chr16

19613045

+C9chr5

39285335

-
Frame-shiftENST00000251143ENST00000263408C16orf62chr16

19613045

+C9chr5

39285335

-
5CDS-intronENST00000251143ENST00000509186C16orf62chr16

19613045

+C9chr5

39285335

-
Frame-shiftENST00000543152ENST00000263408C16orf62chr16

19613045

+C9chr5

39285335

-
5CDS-intronENST00000543152ENST00000509186C16orf62chr16

19613045

+C9chr5

39285335

-
Frame-shiftENST00000448695ENST00000263408C16orf62chr16

19613045

+C9chr5

39285335

-
5CDS-intronENST00000448695ENST00000509186C16orf62chr16

19613045

+C9chr5

39285335

-
intron-3CDSENST00000544275ENST00000263408C16orf62chr16

19613045

+C9chr5

39285335

-
intron-intronENST00000544275ENST00000509186C16orf62chr16

19613045

+C9chr5

39285335

-
3UTR-3CDSENST00000538853ENST00000263408C16orf62chr16

19613045

+C9chr5

39285335

-
3UTR-intronENST00000538853ENST00000509186C16orf62chr16

19613045

+C9chr5

39285335

-

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FusionProtFeatures for C16orf62_C9


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
C16orf62

Q7Z3J2

C9

P02748

Constituent of the membrane attack complex (MAC) thatplays a key role in the innate and adaptive immune response byforming pores in the plasma membrane of target cells(PubMed:9634479, PubMed:9212048, PubMed:26841934). C9 is the pore-forming subunit of the MAC (PubMed:4055801, PubMed:26841934).{ECO:0000269|PubMed:26841934, ECO:0000269|PubMed:4055801,ECO:0000269|PubMed:9212048, ECO:0000269|PubMed:9634479}.

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 C16orf62_C9


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 C16orf62_C9


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
C16orf62CCDC22, CCDC93, COMMD1, BSG, COMMD3, COMMD4, DCUN1D1, TRIM25, NTRK1, COMMD6, VPS29, COMMD2, COMMD10, COMMD8, FAM45A, HDAC11C9CLU, CD59, FN1, LAMTOR5, APOE, CST6


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 C16orf62_C9


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

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RelatedDiseases for C16orf62_C9


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC9C0021051Immunologic Deficiency Syndromes2CTD_human
TgeneC9C0011633Dermatomyositis1CTD_human
TgeneC9C0015456Facial Dermatoses1CTD_human
TgeneC9C0025294Meningococcal meningitis1CTD_human
TgeneC9C0027412Opioid-Related Disorders1CTD_human
TgeneC9C0041834Erythema1CTD_human
TgeneC9C0242383Age related macular degeneration1CTD_human
TgeneC9C0345967Malignant mesothelioma1CTD_human
TgeneC9C2239176Liver carcinoma1CTD_human
TgeneC9C3151189C9 Deficiency1UNIPROT
TgeneC9C3810042MACULAR DEGENERATION, AGE-RELATED, 151UNIPROT