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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: 21435

FusionGeneSummary for MECP2_NKIRAS2

check button Fusion gene summary
Fusion gene informationFusion gene name: MECP2_NKIRAS2
Fusion gene ID: 21435
HgeneTgene
Gene symbol

MECP2

NKIRAS2

Gene ID

4204

28511

Gene namemethyl-CpG binding protein 2NFKB inhibitor interacting Ras like 2
SynonymsAUTSX3|MRX16|MRX79|MRXS13|MRXSL|PPMX|RS|RTS|RTTKBRAS2|kappaB-Ras2
Cytomap

Xq28

17q21.2

Type of geneprotein-codingprotein-coding
Descriptionmethyl-CpG-binding protein 2meCp-2 proteintestis tissue sperm-binding protein Li 41aNF-kappa-B inhibitor-interacting Ras-like protein 2I-kappa-B-interacting Ras-like protein 2NFKB inhibitor interacting Ras-like protein 2kappa B-Ras protein 2
Modification date2018052720180519
UniProtAcc

P51608

Q9NYR9

Ensembl transtripts involved in fusion geneENST00000303391, ENST00000453960, 
ENST00000407218, ENST00000460227, 
ENST00000307641, ENST00000393885, 
ENST00000393884, ENST00000479407, 
ENST00000393881, ENST00000393880, 
ENST00000462043, ENST00000449471, 
ENST00000316082, 
Fusion gene scores* DoF score3 X 3 X 2=181 X 1 X 1=1
# samples 31
** MAII scorelog2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(1/1*10)=3.32192809488736
Context

PubMed: MECP2 [Title/Abstract] AND NKIRAS2 [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
HgeneMECP2

GO:0010629

negative regulation of gene expression

23960241

HgeneMECP2

GO:0043537

negative regulation of blood vessel endothelial cell migration

23960241

HgeneMECP2

GO:0045892

negative regulation of transcription, DNA-templated

11441023

HgeneMECP2

GO:1905643

positive regulation of DNA methylation

23960241


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
ChiTaRS3.1BE350810MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
* 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-3UTRENST00000303391ENST00000307641MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000303391ENST00000393885MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-3UTRENST00000303391ENST00000393884MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000303391ENST00000479407MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000303391ENST00000393881MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000303391ENST00000393880MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000303391ENST00000462043MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000303391ENST00000449471MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000303391ENST00000316082MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-3UTRENST00000453960ENST00000307641MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000453960ENST00000393885MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-3UTRENST00000453960ENST00000393884MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000453960ENST00000479407MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000453960ENST00000393881MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000453960ENST00000393880MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000453960ENST00000462043MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000453960ENST00000449471MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000453960ENST00000316082MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-3UTRENST00000407218ENST00000307641MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000407218ENST00000393885MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-3UTRENST00000407218ENST00000393884MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000407218ENST00000479407MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000407218ENST00000393881MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000407218ENST00000393880MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000407218ENST00000462043MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000407218ENST00000449471MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000407218ENST00000316082MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-3UTRENST00000460227ENST00000307641MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000460227ENST00000393885MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-3UTRENST00000460227ENST00000393884MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000460227ENST00000479407MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000460227ENST00000393881MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000460227ENST00000393880MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000460227ENST00000462043MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000460227ENST00000449471MECP2chrX

153287548

+NKIRAS2chr17

40177378

-
intron-intronENST00000460227ENST00000316082MECP2chrX

153287548

+NKIRAS2chr17

40177378

-

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FusionProtFeatures for MECP2_NKIRAS2


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MECP2

P51608

NKIRAS2

Q9NYR9

Chromosomal protein that binds to methylated DNA. It canbind specifically to a single methyl-CpG pair. It is notinfluenced by sequences flanking the methyl-CpGs. Mediatestranscriptional repression through interaction with histonedeacetylase and the corepressor SIN3A. Binds both 5-methylcytosine(5mC) and 5-hydroxymethylcytosine (5hmC)-containing DNA, with apreference for 5-methylcytosine (5mC).{ECO:0000250|UniProtKB:Q9Z2D6}. Atypical Ras-like protein that acts as a potentregulator of NF-kappa-B activity by preventing the degradation ofNF-kappa-B inhibitor beta (NFKBIB) by most signals, explaining whyNFKBIB is more resistant to degradation. May act by blockingphosphorylation of NFKBIB and nuclear localization of p65/RELA NF-kappa-B subunit. It is unclear whether it acts as a GTPase. BothGTP- and GDP-bound forms block phosphorylation of NFKBIB (Bysimilarity). {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 MECP2_NKIRAS2


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 MECP2_NKIRAS2


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 MECP2_NKIRAS2


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 MECP2_NKIRAS2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMECP2C0035372Rett Syndrome35CTD_human;ORPHANET;UNIPROT
HgeneMECP2C1968550Mental Retardation, X-Linked, Syndromic 139CTD_human;ORPHANET;UNIPROT
HgeneMECP2C0004352Autistic Disorder3CTD_human;HPO
HgeneMECP2C3714756Intellectual Disability2CTD_human;HPO
HgeneMECP2C0003469Anxiety Disorders1CTD_human
HgeneMECP2C0008073Developmental Disabilities1CTD_human
HgeneMECP2C0008074Child Development Disorders, Pervasive1CTD_human
HgeneMECP2C0023186Learning Disorders1CTD_human
HgeneMECP2C0026827Muscle hypotonia1CTD_human
HgeneMECP2C0027066Myoclonus1CTD_human;HPO
HgeneMECP2C0033922Psychomotor Disorders1CTD_human
HgeneMECP2C0034069Pulmonary Fibrosis1CTD_human
HgeneMECP2C0035229Respiratory Insufficiency1CTD_human;HPO
HgeneMECP2C0036572Seizures1CTD_human;HPO
HgeneMECP2C0236736Cocaine-Related Disorders1CTD_human
HgeneMECP2C0376634Craniofacial Abnormalities1CTD_human
HgeneMECP2C2239176Liver carcinoma1CTD_human