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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: 17455

FusionGeneSummary for IMPA2_GALNT1

check button Fusion gene summary
Fusion gene informationFusion gene name: IMPA2_GALNT1
Fusion gene ID: 17455
HgeneTgene
Gene symbol

IMPA2

GALNT1

Gene ID

3613

2589

Gene nameinositol monophosphatase 2polypeptide N-acetylgalactosaminyltransferase 1
Synonyms-GALNAC-T1
Cytomap

18p11.21

18q12.2

Type of geneprotein-codingprotein-coding
Descriptioninositol monophosphatase 2IMP 2IMPase 2inosine monophosphatase 2inositol monophosphatase 2 variant 1inositol monophosphatase 2 variant 2inositol(myo)-1(or 4)-monophosphatase 2myo-inositol monophosphatase 2myo-inositol monophosphatase A2polypeptide N-acetylgalactosaminyltransferase 1GalNAc transferase 1UDP-GalNAc:polypeptide N-acetylgalactosaminyltransferase 1UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 1 (GalNAc-T1)polypeptide GalNAc transferase 1
Modification date2018052320180523
UniProtAcc

O14732

Q10472

Ensembl transtripts involved in fusion geneENST00000588752, ENST00000589238, 
ENST00000269159, ENST00000588927, 
ENST00000586725, ENST00000269195, 
ENST00000591081, ENST00000537549, 
Fusion gene scores* DoF score2 X 1 X 2=46 X 5 X 4=120
# samples 27
** MAII scorelog2(2/4*10)=2.32192809488736log2(7/120*10)=-0.777607578663552
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: IMPA2 [Title/Abstract] AND GALNT1 [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
HgeneIMPA2

GO:0046855

inositol phosphate dephosphorylation

17068342

TgeneGALNT1

GO:0006493

protein O-linked glycosylation

22186971

TgeneGALNT1

GO:0018242

protein O-linked glycosylation via serine

9295285

TgeneGALNT1

GO:0018243

protein O-linked glycosylation via threonine

9295285


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
TCGALDLUADTCGA-86-8055-01AIMPA2chr18

11981764

+GALNT1chr18

33234524

+
* 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-3UTRENST00000588752ENST00000586725IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-3UTRENST00000588752ENST00000269195IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-intronENST00000588752ENST00000591081IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-intronENST00000588752ENST00000537549IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-3UTRENST00000589238ENST00000586725IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-3UTRENST00000589238ENST00000269195IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-intronENST00000589238ENST00000591081IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-intronENST00000589238ENST00000537549IMPA2chr18

11981764

+GALNT1chr18

33234524

+
5CDS-3UTRENST00000269159ENST00000586725IMPA2chr18

11981764

+GALNT1chr18

33234524

+
5CDS-3UTRENST00000269159ENST00000269195IMPA2chr18

11981764

+GALNT1chr18

33234524

+
5CDS-intronENST00000269159ENST00000591081IMPA2chr18

11981764

+GALNT1chr18

33234524

+
5CDS-intronENST00000269159ENST00000537549IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-3UTRENST00000588927ENST00000586725IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-3UTRENST00000588927ENST00000269195IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-intronENST00000588927ENST00000591081IMPA2chr18

11981764

+GALNT1chr18

33234524

+
intron-intronENST00000588927ENST00000537549IMPA2chr18

11981764

+GALNT1chr18

33234524

+

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FusionProtFeatures for IMPA2_GALNT1


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
IMPA2

O14732

GALNT1

Q10472

Can use myo-inositol monophosphates, scylloinositol 1,4-diphosphate, glucose-1-phosphate, beta-glycerophosphate, and 2'-AMP as substrates. Has been implicated as the pharmacologicaltarget for lithium Li(+) action in brain.{ECO:0000269|PubMed:17068342}. Catalyzes the initial reaction in O-linkedoligosaccharide biosynthesis, the transfer of an N-acetyl-D-galactosamine residue to a serine or threonine residue on theprotein receptor. Has a broad spectrum of substrates for peptidessuch as EA2, Muc5AC, Muc1a, Muc1b and Muc7.{ECO:0000269|PubMed:9295285}.

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 IMPA2_GALNT1


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 IMPA2_GALNT1


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
IMPA2TNFRSF14, IMPA1, IMPA2, UBA3, SPACA1, A4GNT, HSF2, ALDOA, ALDOC, ARHGDIA, DUT, FSCN1, GPX4, ADSS, CARHSP1, CYCS, GLO1, HSPE1, NUDT9, PAICS, PARK7, PGLS, PLIN3, RPE, STMN1, TXN, ITPA, MSN, PABPC4, PDCD6, RDX, SCPEP1, NPPA, RBFOX1, ZIC1, AAR2, TRIM25GALNT1ELAVL1, SEC23B, MOV10, NXF1, GINM1, P2RX4, NYX, GALNT13, TRIM25


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 IMPA2_GALNT1


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
HgeneIMPA2O14732DB01356LithiumInositol monophosphatase 2small moleculeapproved

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RelatedDiseases for IMPA2_GALNT1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneIMPA2C0005586Bipolar Disorder5PSYGENET
HgeneIMPA2C0525045Mood Disorders2PSYGENET
HgeneIMPA2C0009952Febrile Convulsions1CTD_human
HgeneIMPA2C0011570Mental Depression1PSYGENET
HgeneIMPA2C0011581Depressive disorder1PSYGENET
HgeneIMPA2C0014175Endometriosis1CTD_human
HgeneIMPA2C0036341Schizophrenia1PSYGENET