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Fusion gene ID: 43839 |
FusionGeneSummary for ZRSR2_CNTNAP2 |
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Fusion gene information | Fusion gene name: ZRSR2_CNTNAP2 | Fusion gene ID: 43839 | Hgene | Tgene | Gene symbol | ZRSR2 | CNTNAP2 | Gene ID | 8233 | 26047 |
Gene name | zinc finger CCCH-type, RNA binding motif and serine/arginine rich 2 | contactin associated protein like 2 | |
Synonyms | U2AF1-RS2|U2AF1L2|U2AF1RS2|URP|ZC3H22 | AUTS15|CASPR2|CDFE|NRXN4|PTHSL1 | |
Cytomap | Xp22.2 | 7q35-q36.1 | |
Type of gene | protein-coding | protein-coding | |
Description | U2 small nuclear ribonucleoprotein auxiliary factor 35 kDa subunit-related protein 2U2 small nuclear ribonucleoprotein auxiliary factor, small subunit 2U2(RNU2) small nuclear RNA auxiliary factor 1-like 2U2AF35-related proteinrenal carcinoma antigen N | contactin-associated protein-like 2cell recognition molecule Caspr2homolog of Drosophila neurexin IV | |
Modification date | 20180523 | 20180519 | |
UniProtAcc | Q15696 | Q9UHC6 | |
Ensembl transtripts involved in fusion gene | ENST00000380308, ENST00000307771, ENST00000468028, | ENST00000361727, ENST00000538075, ENST00000463592, | |
Fusion gene scores | * DoF score | 1 X 1 X 1=1 | 8 X 8 X 7=448 |
# samples | 1 | 9 | |
** MAII score | log2(1/1*10)=3.32192809488736 | log2(9/448*10)=-2.31550182572793 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ZRSR2 [Title/Abstract] AND CNTNAP2 [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) |
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Partner | Gene | GO ID | GO term | PubMed ID |
![]() (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 type | Source | Cancer type | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChiTaRS3.1 | AA323715 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
* LD: Li Ding group's fusion gene list RV: Roel Verhaak group's fusion gene list ChiTaRs fusion database |
![]() * Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser. |
ORF | Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
intron-intron | ENST00000380308 | ENST00000361727 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
intron-intron | ENST00000380308 | ENST00000538075 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
intron-intron | ENST00000380308 | ENST00000463592 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
intron-intron | ENST00000307771 | ENST00000361727 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
intron-intron | ENST00000307771 | ENST00000538075 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
intron-intron | ENST00000307771 | ENST00000463592 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
intron-intron | ENST00000468028 | ENST00000361727 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
intron-intron | ENST00000468028 | ENST00000538075 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
intron-intron | ENST00000468028 | ENST00000463592 | ZRSR2 | chrX | 15809288 | + | CNTNAP2 | chr7 | 146162230 | + |
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FusionProtFeatures for ZRSR2_CNTNAP2 |
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Hgene | Tgene |
ZRSR2 | CNTNAP2 |
Pre-mRNA-binding protein required for splicing of bothU2- and U12-type introns. Selectively interacts with the 3'-splicesite of U2- and U12-type pre-mRNAs and promotes different steps inU2 and U12 intron splicing. Recruited to U12 pre-mRNAs in an ATP-dependent manner and is required for assembly of theprespliceosome, a precursor to other spliceosomal complexes. ForU2-type introns, it is selectively and specifically required forthe second step of splicing. {ECO:0000269|PubMed:21041408,ECO:0000269|PubMed:9237760}. | Required, with CNTNAP1, for radial and longitudinalorganization of myelinated axons. Plays a role in the formation offunctional distinct domains critical for saltatory conduction ofnerve impulses in myelinated nerve fibers. Demarcates thejuxtaparanodal region of the axo-glial junction.{ECO:0000250|UniProtKB:Q9CPW0}. |
![]() * 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. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
- In-frame and not-retained protein feature among the 13 regional features. |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Protein feature | Protein feature note |
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FusionGeneSequence for ZRSR2_CNTNAP2 |
![]() (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 ZRSR2_CNTNAP2 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
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RelatedDrugs for ZRSR2_CNTNAP2 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
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RelatedDiseases for ZRSR2_CNTNAP2 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ZRSR2 | C0349639 | Juvenile Myelomonocytic Leukemia | 1 | CTD_human |
Tgene | CNTNAP2 | C0004352 | Autistic Disorder | 4 | CTD_human |
Tgene | CNTNAP2 | C1510586 | Autism Spectrum Disorders | 4 | CTD_human |
Tgene | CNTNAP2 | C0023014 | Language Development Disorders | 3 | CTD_human |
Tgene | CNTNAP2 | C0014544 | Epilepsy | 2 | CTD_human;HPO |
Tgene | CNTNAP2 | C0001973 | Alcoholic Intoxication, Chronic | 1 | PSYGENET |
Tgene | CNTNAP2 | C0005586 | Bipolar Disorder | 1 | PSYGENET |
Tgene | CNTNAP2 | C0036341 | Schizophrenia | 1 | CTD_human |
Tgene | CNTNAP2 | C0038506 | Stuttering | 1 | CTD_human |
Tgene | CNTNAP2 | C0041696 | Unipolar Depression | 1 | PSYGENET |
Tgene | CNTNAP2 | C0149925 | Small cell carcinoma of lung | 1 | CTD_human |
Tgene | CNTNAP2 | C0424295 | Hyperactive behavior | 1 | CTD_human;HPO |
Tgene | CNTNAP2 | C1269683 | Major Depressive Disorder | 1 | PSYGENET |
Tgene | CNTNAP2 | C1970431 | PITT-HOPKINS SYNDROME | 1 | CTD_human |