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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: 12627

FusionGeneSummary for FAM168A_PARVA

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM168A_PARVA
Fusion gene ID: 12627
HgeneTgene
Gene symbol

FAM168A

PARVA

Gene ID

23201

55742

Gene namefamily with sequence similarity 168 member Aparvin alpha
SynonymsKIAA0280|TCRP1CH-ILKBP|MXRA2
Cytomap

11q13.4

11p15.3

Type of geneprotein-codingprotein-coding
Descriptionprotein FAM168Atongue cancer chemotherapy resistance-associated protein 1alpha-parvinactopaxincalponin-like integrin-linked kinase-binding proteinmatrix-remodeling-associated protein 2
Modification date2018052320180523
UniProtAcc

Q92567

Q9NVD7

Ensembl transtripts involved in fusion geneENST00000064778, ENST00000450446, 
ENST00000356467, 
ENST00000334956, 
ENST00000539723, ENST00000550549, 
ENST00000538608, ENST00000526746, 
Fusion gene scores* DoF score20 X 4 X 10=8009 X 6 X 7=378
# samples 2311
** MAII scorelog2(23/800*10)=-1.79836613883035
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/378*10)=-1.78088271069641
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FAM168A [Title/Abstract] AND PARVA [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
HgeneFAM168A

GO:1905053

positive regulation of base-excision repair

25260657


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
TCGALDUCECTCGA-AX-A3GI-01AFAM168Achr11

73308968

-PARVAchr11

12495292

+
* 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
5UTR-3CDSENST00000064778ENST00000334956FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-3CDSENST00000064778ENST00000539723FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-3CDSENST00000064778ENST00000550549FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-5UTRENST00000064778ENST00000538608FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-5UTRENST00000064778ENST00000526746FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-3CDSENST00000450446ENST00000334956FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-3CDSENST00000450446ENST00000539723FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-3CDSENST00000450446ENST00000550549FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-5UTRENST00000450446ENST00000538608FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-5UTRENST00000450446ENST00000526746FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-3CDSENST00000356467ENST00000334956FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-3CDSENST00000356467ENST00000539723FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-3CDSENST00000356467ENST00000550549FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-5UTRENST00000356467ENST00000538608FAM168Achr11

73308968

-PARVAchr11

12495292

+
5UTR-5UTRENST00000356467ENST00000526746FAM168Achr11

73308968

-PARVAchr11

12495292

+

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FusionProtFeatures for FAM168A_PARVA


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAM168A

Q92567

PARVA

Q9NVD7

In cancer context, protects cells from induced-DNAdamage and apoptosis. Acts, at least in part, throughPI3K/AKT/NFKB signaling pathway and by preventing POLBdegradation. Decreases POLB ubiquitation and stabilizes itsprotein levels. {ECO:0000269|PubMed:21334329,ECO:0000269|PubMed:21603883, ECO:0000269|PubMed:23251525,ECO:0000269|PubMed:25260657}. Plays a role in sarcomere organization and in smoothmuscle cell contraction. Required for normal development of theembryonic cardiovascular system, and for normal septation of theheart outflow tract. Plays a role in sprouting angiogenesis and isrequired for normal adhesion of vascular smooth muscle cells toendothelial cells during blood vessel development (By similarity).Plays a role in the reorganization of the actin cytoskeleton,formation of lamellipodia and ciliogenesis. Plays a role in theestablishement of cell polarity, cell adhesion, cell spreading,and directed cell migration. {ECO:0000250,ECO:0000269|PubMed:11134073, ECO:0000269|PubMed:11331308,ECO:0000269|PubMed:15284246, ECO:0000269|PubMed:20393563}.

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 FAM168A_PARVA


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 FAM168A_PARVA


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
FAM168ABAG3, RBFOX1, DAB1, SNRPC, UBE2V1, SF1, TAX1BP1, DAZAP2, CALCOCO2, TNIP1, RBPMS, R3HDM2, FAM168A, SS18L1, VPS37C, KLHL42, SMAP2, OTUB2, UBASH3B, C1orf94, OTULIN, NAF1, DTX2, PRR20A, MOV10, FBXO6, WWP2, EWSR1, FBXW5, MCM2, TRIM25PARVAILK, DHX36, UBE3A, ELAVL1, APP, MLH1, SOX2, HSPH1, CARM1, CORO1B, CRMP1, OSBP, OTUD6B, PPAT, TBC1D17, UGP2, ZRANB2, RSU1, SEC24C, MOCOS, LIMS1, PARVB, IQGAP1, VPS11, GCA, DDX47, CHMP2A, CMTR2, DDX17, DPH5, HSPB2, UBQLN1, SNW1, CDC5L, CDH1, LPXN, CCNB1


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 FAM168A_PARVA


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 FAM168A_PARVA


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneFAM168AC0038356Stomach Neoplasms1CTD_human
TgenePARVAC0236969Substance-Related Disorders1CTD_human