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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: 33806

FusionGeneSummary for SHROOM2_ADNP

check button Fusion gene summary
Fusion gene informationFusion gene name: SHROOM2_ADNP
Fusion gene ID: 33806
HgeneTgene
Gene symbol

SHROOM2

ADNP

Gene ID

357

23394

Gene nameshroom family member 2activity dependent neuroprotector homeobox
SynonymsAPXL|HSAPXLADNP1|HVDAS|MRD28
Cytomap

Xp22.2

20q13.13

Type of geneprotein-codingprotein-coding
Descriptionprotein Shroom2APX homolog of Xenopusapical-like proteinactivity-dependent neuroprotector homeobox proteinADNP homeobox 1activity-dependent neuroprotective proteinactivity-dependent neuroprotector
Modification date2018052320180522
UniProtAcc

Q13796

Q9H2P0

Ensembl transtripts involved in fusion geneENST00000380913, ENST00000493668, 
ENST00000418909, 
ENST00000396029, 
ENST00000396032, ENST00000371602, 
ENST00000349014, 
Fusion gene scores* DoF score5 X 6 X 3=905 X 4 X 3=60
# samples 54
** MAII scorelog2(5/90*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(4/60*10)=-0.584962500721156
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: SHROOM2 [Title/Abstract] AND ADNP [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
HgeneSHROOM2

GO:0000902

cell morphogenesis

16684770


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
ChiTaRS3.1BE148732SHROOM2chrX

9807993

-ADNPchr20

49519223

+
* 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-intronENST00000380913ENST00000396029SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000380913ENST00000396032SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000380913ENST00000371602SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000380913ENST00000349014SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000493668ENST00000396029SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000493668ENST00000396032SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000493668ENST00000371602SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000493668ENST00000349014SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000418909ENST00000396029SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000418909ENST00000396032SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000418909ENST00000371602SHROOM2chrX

9807993

-ADNPchr20

49519223

+
intron-intronENST00000418909ENST00000349014SHROOM2chrX

9807993

-ADNPchr20

49519223

+

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FusionProtFeatures for SHROOM2_ADNP


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SHROOM2

Q13796

ADNP

Q9H2P0

May be involved in endothelial cell morphology changesduring cell spreading. In the retinal pigment epithelium, mayregulate the biogenesis of melanosomes and promote theirassociation with the apical cell surface by inducing gamma-tubulinredistribution (By similarity). {ECO:0000250}. Potential transcription factor. May mediate some of theneuroprotective peptide VIP-associated effects involving normalgrowth and cancer proliferation.

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 SHROOM2_ADNP


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 SHROOM2_ADNP


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 SHROOM2_ADNP


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 SHROOM2_ADNP


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneADNPC0004352Autistic Disorder1CTD_human
TgeneADNPC0015923Fetal Alcohol Syndrome1PSYGENET
TgeneADNPC0036341Schizophrenia1PSYGENET
TgeneADNPC1542327Fetus or newborn affected by alcohol transmitted via placenta or breast milk1PSYGENET