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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: 32858

FusionGeneSummary for SCML2_MAP7D2

check button Fusion gene summary
Fusion gene informationFusion gene name: SCML2_MAP7D2
Fusion gene ID: 32858
HgeneTgene
Gene symbol

SCML2

MAP7D2

Gene ID

10389

256714

Gene nameScm polycomb group protein like 2MAP7 domain containing 2
Synonyms--
Cytomap

Xp22.13

Xp22.12

Type of geneprotein-codingprotein-coding
Descriptionsex comb on midleg-like protein 2sex comb on midleg like 2MAP7 domain-containing protein 2MAP7 domain containing 2 brainMAP7 domain containing 2 protein varaint 1MAP7 domain containing 2 protein varaint 2MAP7 domain-containing protein 2 brain specific variant 1MAP7 domain-containing protein 2 brain specific
Modification date2018051920180523
UniProtAcc

Q9UQR0

Q96T17

Ensembl transtripts involved in fusion geneENST00000251900, ENST00000491988, 
ENST00000398048, 
ENST00000379651, 
ENST00000379643, ENST00000543767, 
ENST00000443379, ENST00000452324, 
ENST00000466145, 
Fusion gene scores* DoF score3 X 3 X 2=182 X 2 X 1=4
# samples 32
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/4*10)=2.32192809488736
Context

PubMed: SCML2 [Title/Abstract] AND MAP7D2 [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-AN-A0AM-01ASCML2chrX

18323092

-MAP7D2chrX

20082923

-
* 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-shiftENST00000251900ENST00000379651SCML2chrX

18323092

-MAP7D2chrX

20082923

-
Frame-shiftENST00000251900ENST00000379643SCML2chrX

18323092

-MAP7D2chrX

20082923

-
5CDS-intronENST00000251900ENST00000543767SCML2chrX

18323092

-MAP7D2chrX

20082923

-
5CDS-intronENST00000251900ENST00000443379SCML2chrX

18323092

-MAP7D2chrX

20082923

-
5CDS-5UTRENST00000251900ENST00000452324SCML2chrX

18323092

-MAP7D2chrX

20082923

-
5CDS-intronENST00000251900ENST00000466145SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-3CDSENST00000491988ENST00000379651SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-3CDSENST00000491988ENST00000379643SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-intronENST00000491988ENST00000543767SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-intronENST00000491988ENST00000443379SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-5UTRENST00000491988ENST00000452324SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-intronENST00000491988ENST00000466145SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-3CDSENST00000398048ENST00000379651SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-3CDSENST00000398048ENST00000379643SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-intronENST00000398048ENST00000543767SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-intronENST00000398048ENST00000443379SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-5UTRENST00000398048ENST00000452324SCML2chrX

18323092

-MAP7D2chrX

20082923

-
intron-intronENST00000398048ENST00000466145SCML2chrX

18323092

-MAP7D2chrX

20082923

-

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FusionProtFeatures for SCML2_MAP7D2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SCML2

Q9UQR0

MAP7D2

Q96T17

Putative Polycomb group (PcG) protein. PcG proteins actby forming multiprotein complexes, which are required to maintainthe transcriptionally repressive state of homeotic genesthroughout development (By similarity). {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 SCML2_MAP7D2


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 SCML2_MAP7D2


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
SCML2USP7, RNF2, PHC2, LMNA, HECW2, BAG1, BMI1, CBX8, POU5F1, POTEB3, TXNIPMAP7D2KLHL20, EFNB2, FHL3, KIAA0753, CEP162, SPICE1, DCTN1, LCA5, KIF20A, BEND3, NEURL4, HERC2, USP20, UBE3A, CLINT1, LONP2, ECI2, IL17RA, STX8, TRIM27, KIF5B, SIRT6, OLFML3, P4HA2, CENPF


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 SCML2_MAP7D2


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 SCML2_MAP7D2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSCML2C0025149Medulloblastoma1CTD_human