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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: 21697

FusionGeneSummary for METTL21B_PIP4K2C

check button Fusion gene summary
Fusion gene informationFusion gene name: METTL21B_PIP4K2C
Fusion gene ID: 21697
HgeneTgene
Gene symbol

METTL21B

PIP4K2C

Gene ID

79837

Gene namephosphatidylinositol-5-phosphate 4-kinase type 2 gamma
SynonymsPIP5K2C
Cytomap

12q13.3

Type of geneprotein-coding
Descriptionphosphatidylinositol 5-phosphate 4-kinase type-2 gammaPI(5)P 4-kinase type II gammaPIP4KII-gammaphosphatidylinositol 4-phosphate 5-kinasephosphatidylinositol 5-phosphate 4-kinase type II gammaphosphatidylinositol-4-phosphate 5-kinase, type II, gamma
Modification date20180519
UniProtAcc

Q8TBX8

Ensembl transtripts involved in fusion geneENST00000548256, ENST00000551420, 
ENST00000300209, ENST00000552307, 
ENST00000333012, 
ENST00000422156, 
ENST00000540759, ENST00000550465, 
ENST00000354947, 
Fusion gene scores* DoF score14 X 2 X 6=1689 X 6 X 5=270
# samples 139
** MAII scorelog2(13/168*10)=-0.369949609750306
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/270*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: METTL21B [Title/Abstract] AND PIP4K2C [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
TCGALDSKCMTCGA-EE-A2GB-06AMETTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
* 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-shiftENST00000548256ENST00000422156METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000548256ENST00000540759METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000548256ENST00000550465METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000548256ENST00000354947METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
5UTR-3CDSENST00000551420ENST00000422156METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
5UTR-3CDSENST00000551420ENST00000540759METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
5UTR-3CDSENST00000551420ENST00000550465METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
5UTR-3CDSENST00000551420ENST00000354947METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000300209ENST00000422156METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000300209ENST00000540759METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000300209ENST00000550465METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000300209ENST00000354947METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
intron-3CDSENST00000552307ENST00000422156METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
intron-3CDSENST00000552307ENST00000540759METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
intron-3CDSENST00000552307ENST00000550465METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
intron-3CDSENST00000552307ENST00000354947METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000333012ENST00000422156METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000333012ENST00000540759METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000333012ENST00000550465METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+
Frame-shiftENST00000333012ENST00000354947METTL21Bchr12

58166911

+PIP4K2Cchr12

57987808

+

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FusionProtFeatures for METTL21B_PIP4K2C


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
METTL21B

PIP4K2C

Q8TBX8

Lectin that binds to various sugars: galactose > mannose= fucose > N-acetylglucosamine > N-acetylgalactosamine(PubMed:10224141). Acts as a chemoattractant, probably involved inthe regulation of cell migration (PubMed:28301481).{ECO:0000269|PubMed:10224141, ECO:0000269|PubMed:28301481}. May play an important role in the production ofPhosphatidylinositol bisphosphate (PIP2), in the endoplasmicreticulum. {ECO:0000250}.

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 METTL21B_PIP4K2C


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 METTL21B_PIP4K2C


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
METTL21BELAVL1, BAG2, BAG6, CCT2, CCT3, CCT4, CCT5, CCT6A, CCT6B, CCT7, CCT8, CTSB, DNAJA1, DNAJA2, HSP90AA1, HSP90AB1, HSP90AB2P, HSP90AB4P, HSPA1L, HSPA2, HSPA5, HSPA7, HSPA8, HSPD1, HUWE1, IGBP1, CCAR2, LAMP2, LDHA, LDHB, MDH2, NTPCR, PDCD5, PFDN1, PFDN2, PFDN4, PFDN5, PFDN6, PPP6C, RNF126, RUVBL1, RUVBL2, SAR1A, SMC1A, SMC3, STIP1, TCP1, TIPRL, TUBB2A, TUBB3, TUBB4A, TUBB6, TUBB8, TUBBP5, UBA1, UBB, UBC, UBL4A, VBP1PIP4K2CELAVL1, APP, PIP4K2C, FBXO25, CSNK2A2, ARL6IP4, EAF1, LZTS2, ZRANB2, EPB41L3, CSNK2A1, CSNK2B, DDX23, MTPN, MYL9, NCAPD3, PRPF8, SKP1, MED4, NF2, PIP4K2A, ARHGAP22, AHCYL2, GPBP1L1, PRICKLE3, HIF1AN, TULP3, ZNF428, CAMKV, POC1B, SUN2, TNFRSF19, C16orf71, GSPT2, APBA3, TNFRSF1A, HSD17B10


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 METTL21B_PIP4K2C


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 METTL21B_PIP4K2C


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePIP4K2CC0036341Schizophrenia2PSYGENET
TgenePIP4K2CC0005586Bipolar Disorder1PSYGENET