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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: 20960

FusionGeneSummary for MAP9_TAT

check button Fusion gene summary
Fusion gene informationFusion gene name: MAP9_TAT
Fusion gene ID: 20960
HgeneTgene
Gene symbol

MAP9

TAT

Gene ID

79884

79969

Gene namemicrotubule associated protein 9alpha tubulin acetyltransferase 1
SynonymsASAPC6orf134|MEC17|Nbla00487|TAT|alpha-TAT|alpha-TAT1
Cytomap

4q32.1

6p21.33

Type of geneprotein-codingprotein-coding
Descriptionmicrotubule-associated protein 9aster-associated proteinalpha-tubulin N-acetyltransferase 1acetyltransferase mec-17 homolog
Modification date2018052220180527
UniProtAcc

Q49MG5

P17735

Ensembl transtripts involved in fusion geneENST00000311277, ENST00000515654, 
ENST00000379248, 
ENST00000355962, 
Fusion gene scores* DoF score2 X 2 X 2=81 X 1 X 1=1
# samples 21
** MAII scorelog2(2/8*10)=1.32192809488736log2(1/1*10)=3.32192809488736
Context

PubMed: MAP9 [Title/Abstract] AND TAT [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
HgeneMAP9

GO:0090307

mitotic spindle assembly

16049101

TgeneTAT

GO:0071929

alpha-tubulin acetylation

23071314|24906155


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
TCGARVLGGTCGA-HT-7857-01AMAP9chr4

156281320

-TATchr16

71610330

-
* 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
5CDS-5UTRENST00000311277ENST00000355962MAP9chr4

156281320

-TATchr16

71610330

-
5CDS-5UTRENST00000515654ENST00000355962MAP9chr4

156281320

-TATchr16

71610330

-
intron-5UTRENST00000379248ENST00000355962MAP9chr4

156281320

-TATchr16

71610330

-

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FusionProtFeatures for MAP9_TAT


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MAP9

Q49MG5

TAT

P17735

Involved in organization of the bipolar mitotic spindle.Required for bipolar spindle assembly, mitosis progression andcytokinesis. May act by stabilizing interphase microtubules.{ECO:0000269|PubMed:16049101}. Transaminase involved in tyrosine breakdown. Convertstyrosine to p-hydroxyphenylpyruvate. Can catalyze the reversereaction, using glutamic acid, with 2-oxoglutarate as cosubstrate(in vitro). Has much lower affinity and transaminase activitytowards phenylalanine. {ECO:0000269|PubMed:16640556,ECO:0000269|PubMed:7999802}.

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 MAP9_TAT


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 MAP9_TAT


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
MAP9TP53, EP300, SH3KBP1, AURKB, SPICE1, DCTN1, LCA5TATGRN, UBE3A, TAT, AARSD1


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 MAP9_TAT


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneTATP17735DB00114Pyridoxal PhosphateTyrosine aminotransferasesmall moleculeapproved|investigational|nutraceutical
TgeneTATP17735DB00142Glutamic AcidTyrosine aminotransferasesmall moleculeapproved|nutraceutical

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RelatedDiseases for MAP9_TAT


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneTATC0268487Tyrosine Transaminase Deficiency Disease1ORPHANET;UNIPROT