FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Center for Computational Systems Medicine
leaf

FusionGeneSummary

leaf

FusionProtFeature

leaf

FusionGeneSequence

leaf

FusionGenePPI

leaf

RelatedDrugs

leaf

RelatedDiseases

Fusion gene ID: 3043

FusionGeneSummary for ASTN2_LRRC37A5P

check button Fusion gene summary
Fusion gene informationFusion gene name: ASTN2_LRRC37A5P
Fusion gene ID: 3043
HgeneTgene
Gene symbol

ASTN2

LRRC37A5P

Gene ID

23245

652972

Gene nameastrotactin 2leucine rich repeat containing 37 member A5, pseudogene
SynonymsbA67K19.1C9orf29
Cytomap

9q33.1

9q31.3

Type of geneprotein-codingpseudo
Descriptionastrotactin-2-
Modification date2018051920180329
UniProtAcc

O75129

Ensembl transtripts involved in fusion geneENST00000373996, ENST00000313400, 
ENST00000361209, ENST00000361477, 
ENST00000288520, ENST00000341734, 
ENST00000358637, 
ENST00000374304, 
Fusion gene scores* DoF score11 X 11 X 6=7261 X 1 X 1=1
# samples 111
** MAII scorelog2(11/726*10)=-2.72246602447109
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: ASTN2 [Title/Abstract] AND LRRC37A5P [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
TCGALDBRCATCGA-A2-A0EW-01AASTN2chr9

119802098

-LRRC37A5Pchr9

114365393

-
* 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-intronENST00000373996ENST00000374304ASTN2chr9

119802098

-LRRC37A5Pchr9

114365393

-
5CDS-intronENST00000313400ENST00000374304ASTN2chr9

119802098

-LRRC37A5Pchr9

114365393

-
5CDS-intronENST00000361209ENST00000374304ASTN2chr9

119802098

-LRRC37A5Pchr9

114365393

-
5UTR-intronENST00000361477ENST00000374304ASTN2chr9

119802098

-LRRC37A5Pchr9

114365393

-
intron-intronENST00000288520ENST00000374304ASTN2chr9

119802098

-LRRC37A5Pchr9

114365393

-
intron-intronENST00000341734ENST00000374304ASTN2chr9

119802098

-LRRC37A5Pchr9

114365393

-
intron-intronENST00000358637ENST00000374304ASTN2chr9

119802098

-LRRC37A5Pchr9

114365393

-

Top

FusionProtFeatures for ASTN2_LRRC37A5P


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ASTN2

O75129

LRRC37A5P

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}.

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


Top

FusionGeneSequence for ASTN2_LRRC37A5P


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).

Top

FusionGenePPI for ASTN2_LRRC37A5P


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
ASTN2CCT6B, FBXL12, CCT4LRRC37A5P


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


Top

RelatedDrugs for ASTN2_LRRC37A5P


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

Top

RelatedDiseases for ASTN2_LRRC37A5P


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneASTN2C0036341Schizophrenia2PSYGENET
HgeneASTN2C0004352Autistic Disorder1CTD_human
HgeneASTN2C0005586Bipolar Disorder1PSYGENET
HgeneASTN2C0236733Amphetamine-Related Disorders1CTD_human
HgeneASTN2C0338480Common Migraine1CTD_human