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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: 38509

FusionGeneSummary for TMEM184A_TMEM184A

check button Fusion gene summary
Fusion gene informationFusion gene name: TMEM184A_TMEM184A
Fusion gene ID: 38509
HgeneTgene
Gene symbol

TMEM184A

TMEM184A

Gene ID

202915

202915

Gene nametransmembrane protein 184Atransmembrane protein 184A
SynonymsSDMG1SDMG1
Cytomap

7p22.3

7p22.3

Type of geneprotein-codingprotein-coding
Descriptiontransmembrane protein 184Asexually dimorphic, expressed in male gonads 1transmembrane protein 184Asexually dimorphic, expressed in male gonads 1
Modification date2018052320180523
UniProtAcc

Q6ZMB5

Q6ZMB5

Ensembl transtripts involved in fusion geneENST00000297477, ENST00000449955, 
ENST00000297477, ENST00000449955, 
Fusion gene scores* DoF score1 X 2 X 1=21 X 2 X 1=2
# samples 22
** MAII scorelog2(2/2*10)=3.32192809488736log2(2/2*10)=3.32192809488736
Context

PubMed: TMEM184A [Title/Abstract] AND TMEM184A [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

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
ChiTaRS3.1AI216042TMEM184Achr7

1585298

-TMEM184Achr7

1588367

-
ChiTaRS3.1BG003089TMEM184Achr7

1583814

-TMEM184Achr7

1584014

+
* 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-intronENST00000297477ENST00000297477TMEM184Achr7

1585298

-TMEM184Achr7

1588367

-
intron-intronENST00000297477ENST00000449955TMEM184Achr7

1585298

-TMEM184Achr7

1588367

-
intron-intronENST00000449955ENST00000297477TMEM184Achr7

1585298

-TMEM184Achr7

1588367

-
intron-intronENST00000449955ENST00000449955TMEM184Achr7

1585298

-TMEM184Achr7

1588367

-
intron-3UTRENST00000297477ENST00000297477TMEM184Achr7

1583814

-TMEM184Achr7

1584014

+
intron-5UTRENST00000297477ENST00000449955TMEM184Achr7

1583814

-TMEM184Achr7

1584014

+
intron-3UTRENST00000449955ENST00000297477TMEM184Achr7

1583814

-TMEM184Achr7

1584014

+
intron-5UTRENST00000449955ENST00000449955TMEM184Achr7

1583814

-TMEM184Achr7

1584014

+

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FusionProtFeatures for TMEM184A_TMEM184A


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
TMEM184A

Q6ZMB5

TMEM184A

Q6ZMB5

Acts as a heparin receptor in vascular cells (Bysimilarity). May be involved in vesicle transport in exocrinecells and Sertoli cells (By similarity).{ECO:0000250|UniProtKB:Q3UFJ6, ECO:0000250|UniProtKB:Q4QQS1}. Acts as a heparin receptor in vascular cells (Bysimilarity). May be involved in vesicle transport in exocrinecells and Sertoli cells (By similarity).{ECO:0000250|UniProtKB:Q3UFJ6, ECO:0000250|UniProtKB:Q4QQS1}.

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 TMEM184A_TMEM184A


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 TMEM184A_TMEM184A


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 TMEM184A_TMEM184A


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 TMEM184A_TMEM184A


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource