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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: 38304

FusionGeneSummary for TMCO1_TMCO1

check button Fusion gene summary
Fusion gene informationFusion gene name: TMCO1_TMCO1
Fusion gene ID: 38304
HgeneTgene
Gene symbol

TMCO1

TMCO1

Gene ID

54499

54499

Gene nametransmembrane and coiled-coil domains 1transmembrane and coiled-coil domains 1
SynonymsHP10122|PCIA3|PNAS-136|TMCC4HP10122|PCIA3|PNAS-136|TMCC4
Cytomap

1q24.1

1q24.1

Type of geneprotein-codingprotein-coding
Descriptioncalcium load-activated calcium channelCLAC channelputative membrane proteintransmembrane and coiled-coil domain-containing protein 1transmembrane and coiled-coil domains 4xenogeneic cross-immune protein PCIA3calcium load-activated calcium channelCLAC channelputative membrane proteintransmembrane and coiled-coil domain-containing protein 1transmembrane and coiled-coil domains 4xenogeneic cross-immune protein PCIA3
Modification date2018051920180519
UniProtAcc

Q9UM00

Q9UM00

Ensembl transtripts involved in fusion geneENST00000392129, ENST00000367881, 
ENST00000580248, ENST00000464650, 
ENST00000392129, ENST00000367881, 
ENST00000580248, ENST00000464650, 
Fusion gene scores* DoF score1 X 1 X 1=14 X 4 X 4=64
# samples 14
** MAII scorelog2(1/1*10)=3.32192809488736log2(4/64*10)=-0.678071905112638
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: TMCO1 [Title/Abstract] AND TMCO1 [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
HgeneTMCO1

GO:0006983

ER overload response

27212239

HgeneTMCO1

GO:0032469

endoplasmic reticulum calcium ion homeostasis

27212239

HgeneTMCO1

GO:0070588

calcium ion transmembrane transport

27212239

TgeneTMCO1

GO:0006983

ER overload response

27212239

TgeneTMCO1

GO:0032469

endoplasmic reticulum calcium ion homeostasis

27212239

TgeneTMCO1

GO:0070588

calcium ion transmembrane transport

27212239


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
ChiTaRS3.1CA312776TMCO1chr1

165697033

+TMCO1chr1

165697262

-
* 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-3CDSENST00000392129ENST00000392129TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000392129ENST00000367881TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000392129ENST00000580248TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000392129ENST00000464650TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000367881ENST00000392129TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000367881ENST00000367881TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000367881ENST00000580248TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000367881ENST00000464650TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000580248ENST00000392129TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000580248ENST00000367881TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000580248ENST00000580248TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000580248ENST00000464650TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000464650ENST00000392129TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000464650ENST00000367881TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000464650ENST00000580248TMCO1chr1

165697033

+TMCO1chr1

165697262

-
intron-3CDSENST00000464650ENST00000464650TMCO1chr1

165697033

+TMCO1chr1

165697262

-

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FusionProtFeatures for TMCO1_TMCO1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TMCO1

Q9UM00

TMCO1

Q9UM00

Calcium-selective channel required to prevent calciumstores from overfilling, thereby playing a key role in calciumhomeostasis (PubMed:27212239). In response to endoplasmicreticulum overloading, assembles into a homotetramer, forming afunctional calcium-selective channel, regulating the calciumcontent in endoplasmic reticulum store (PubMed:27212239).{ECO:0000269|PubMed:27212239}. Calcium-selective channel required to prevent calciumstores from overfilling, thereby playing a key role in calciumhomeostasis (PubMed:27212239). In response to endoplasmicreticulum overloading, assembles into a homotetramer, forming afunctional calcium-selective channel, regulating the calciumcontent in endoplasmic reticulum store (PubMed:27212239).{ECO:0000269|PubMed:27212239}.

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 TMCO1_TMCO1


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 TMCO1_TMCO1


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 TMCO1_TMCO1


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 TMCO1_TMCO1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneTMCO1C0005941Bone Diseases, Developmental1CTD_human
HgeneTMCO1C0017612Glaucoma, Open-Angle1CTD_human
HgeneTMCO1C0040427Tooth Abnormalities1CTD_human
HgeneTMCO1C0151491Congenital musculoskeletal anomalies1CTD_human
HgeneTMCO1C0376634Craniofacial Abnormalities1CTD_human
HgeneTMCO1C3714756Intellectual Disability1CTD_human;HPO
TgeneTMCO1C0005941Bone Diseases, Developmental1CTD_human
TgeneTMCO1C0017612Glaucoma, Open-Angle1CTD_human
TgeneTMCO1C0040427Tooth Abnormalities1CTD_human
TgeneTMCO1C0151491Congenital musculoskeletal anomalies1CTD_human
TgeneTMCO1C0376634Craniofacial Abnormalities1CTD_human
TgeneTMCO1C3714756Intellectual Disability1CTD_human;HPO