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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: 2438

FusionGeneSummary for ARHGAP32_EPB41L2

check button Fusion gene summary
Fusion gene informationFusion gene name: ARHGAP32_EPB41L2
Fusion gene ID: 2438
HgeneTgene
Gene symbol

ARHGAP32

EPB41L2

Gene ID

9743

2037

Gene nameRho GTPase activating protein 32erythrocyte membrane protein band 4.1 like 2
SynonymsGC-GAP|GRIT|PX-RICS|RICS|p200RhoGAP|p250GAP4.1-G|4.1G
Cytomap

11q24.3

6q23.1-q23.2

Type of geneprotein-codingprotein-coding
Descriptionrho GTPase-activating protein 32GAB-associated CDC42GAB-associated Cdc42/Rac GTPase-activating proteinGTPase regulator interacting with TrkAGTPase-activating protein for Cdc42 and Rac1RhoGAP involved in the -catenin-N-cadherin and NMDA receptor signaband 4.1-like protein 2erythrocyte membrane protein band 4.1 like-protein 2generally expressed protein 4.1
Modification date2018052320180523
UniProtAcc

A7KAX9

O43491

Ensembl transtripts involved in fusion geneENST00000310343, ENST00000524655, 
ENST00000392657, ENST00000527272, 
ENST00000528282, ENST00000530481, 
ENST00000445890, ENST00000337057, 
ENST00000530757, ENST00000392427, 
ENST00000368128, ENST00000527411, 
ENST00000524581, ENST00000525271, 
ENST00000525193, ENST00000527659, 
ENST00000529208, ENST00000531410, 
ENST00000530148, 
Fusion gene scores* DoF score9 X 7 X 4=2527 X 6 X 5=210
# samples 97
** MAII scorelog2(9/252*10)=-1.48542682717024
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(7/210*10)=-1.58496250072116
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ARHGAP32 [Title/Abstract] AND EPB41L2 [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
ChiTaRS3.1DA235187ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
* 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-intronENST00000310343ENST00000528282ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000530481ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000445890ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000337057ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000530757ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000392427ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000368128ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000527411ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000524581ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000525271ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000525193ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000527659ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000529208ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000531410ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000310343ENST00000530148ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000528282ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000530481ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000445890ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000337057ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000530757ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000392427ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000368128ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000527411ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000524581ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000525271ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000525193ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000527659ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000529208ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000531410ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000524655ENST00000530148ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000528282ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000530481ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000445890ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000337057ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000530757ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000392427ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000368128ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000527411ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000524581ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000525271ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000525193ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000527659ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000529208ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000531410ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000392657ENST00000530148ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000528282ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000530481ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000445890ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000337057ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000530757ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000392427ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000368128ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000527411ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000524581ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000525271ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000525193ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000527659ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000529208ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000531410ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-
intron-intronENST00000527272ENST00000530148ARHGAP32chr11

128835485

-EPB41L2chr6

131182325

-

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FusionProtFeatures for ARHGAP32_EPB41L2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ARHGAP32

A7KAX9

EPB41L2

O43491

GTPase-activating protein (GAP) promoting GTP hydrolysison RHOA, CDC42 and RAC1 small GTPases. May be involved in thedifferentiation of neuronal cells during the formation of neuriteextensions. Involved in NMDA receptor activity-dependent actinreorganization in dendritic spines. May mediate cross-talksbetween Ras- and Rho-regulated signaling pathways in cell growthregulation. Isoform 2 has higher GAP activity (By similarity).{ECO:0000250, ECO:0000269|PubMed:12446789,ECO:0000269|PubMed:12454018, ECO:0000269|PubMed:12531901,ECO:0000269|PubMed:12788081, ECO:0000269|PubMed:12819203,ECO:0000269|PubMed:12857875, ECO:0000269|PubMed:17663722}. Required for dynein-dynactin complex and NUMA1recruitment at the mitotic cell cortex during anaphase(PubMed:23870127). {ECO:0000269|PubMed:23870127}.

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 ARHGAP32_EPB41L2


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 ARHGAP32_EPB41L2


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 ARHGAP32_EPB41L2


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 ARHGAP32_EPB41L2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneARHGAP32C0036341Schizophrenia1PSYGENET
TgeneEPB41L2C0023893Liver Cirrhosis, Experimental1CTD_human