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Fusion gene ID: 23014 |
FusionGeneSummary for MYH9_NCL |
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Fusion gene information | Fusion gene name: MYH9_NCL | Fusion gene ID: 23014 | Hgene | Tgene | Gene symbol | MYH9 | NCL | Gene ID | 4627 | 80331 |
Gene name | myosin heavy chain 9 | DnaJ heat shock protein family (Hsp40) member C5 | |
Synonyms | BDPLT6|DFNA17|EPSTS|FTNS|MHA|NMHC-II-A|NMMHC-IIA|NMMHCA | CLN4|CLN4B|CSP|DNAJC5A|NCL|mir-941-2|mir-941-3|mir-941-4|mir-941-5 | |
Cytomap | 22q12.3 | 20q13.33 | |
Type of gene | protein-coding | protein-coding | |
Description | myosin-9cellular myosin heavy chain, type Amyosin, heavy chain 9, non-musclenon-muscle myosin heavy chain 9non-muscle myosin heavy chain Anon-muscle myosin heavy chain IIanon-muscle myosin heavy polypeptide 9nonmuscle myosin heavy chain II-A | dnaJ homolog subfamily C member 5DnaJ (Hsp40) homolog, subfamily C, member 5ceroid-lipofuscinosis neuronal protein 4cysteine string protein alpha | |
Modification date | 20180522 | 20180522 | |
UniProtAcc | P35579 | P19338 | |
Ensembl transtripts involved in fusion gene | ENST00000216181, ENST00000475726, ENST00000401701, | ENST00000322723, | |
Fusion gene scores | * DoF score | 36 X 33 X 15=17820 | 16 X 18 X 1=288 |
# samples | 50 | 20 | |
** MAII score | log2(50/17820*10)=-5.1554254317472 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(20/288*10)=-0.526068811667588 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: MYH9 [Title/Abstract] AND NCL [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 |
Hgene | MYH9 | GO:0001525 | angiogenesis | 16403913 |
Hgene | MYH9 | GO:0006509 | membrane protein ectodomain proteolysis | 16186248 |
Hgene | MYH9 | GO:0030048 | actin filament-based movement | 12237319|15845534 |
Hgene | MYH9 | GO:0031032 | actomyosin structure organization | 24072716 |
![]() (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 | BF815870 | MYH9 | chr22 | 36691572 | - | NCL | chr2 | 232325190 | + |
* 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 | ENST00000216181 | ENST00000322723 | MYH9 | chr22 | 36691572 | - | NCL | chr2 | 232325190 | + |
intron-intron | ENST00000475726 | ENST00000322723 | MYH9 | chr22 | 36691572 | - | NCL | chr2 | 232325190 | + |
intron-intron | ENST00000401701 | ENST00000322723 | MYH9 | chr22 | 36691572 | - | NCL | chr2 | 232325190 | + |
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FusionProtFeatures for MYH9_NCL |
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Hgene | Tgene |
MYH9 | NCL |
Cellular myosin that appears to play a role incytokinesis, cell shape, and specialized functions such assecretion and capping. During cell spreading, plays an importantrole in cytoskeleton reorganization, focal contacts formation (inthe margins but not the central part of spreading cells), andlamellipodial retraction; this function is mechanicallyantagonized by MYH10. {ECO:0000269|PubMed:20052411}. | Nucleolin is the major nucleolar protein of growingeukaryotic cells. It is found associated with intranucleolarchromatin and pre-ribosomal particles. It induces chromatindecondensation by binding to histone H1. It is thought to play arole in pre-rRNA transcription and ribosome assembly. May play arole in the process of transcriptional elongation. Binds RNAoligonucleotides with 5'-UUAGGG-3' repeats more tightly than thetelomeric single-stranded DNA 5'-TTAGGG-3' repeats.{ECO:0000269|PubMed:10393184}. |
![]() * 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 MYH9_NCL |
![]() (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 MYH9_NCL |
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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 MYH9_NCL |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | MYH9 | P35579 | DB11638 | Artenimol | Myosin-9 | small molecule | approved|investigational |
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RelatedDiseases for MYH9_NCL |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | MYH9 | C0403445 | Fechtner syndrome (disorder) | 9 | UNIPROT |
Hgene | MYH9 | C0398641 | Epstein syndrome (disorder) | 7 | UNIPROT |
Hgene | MYH9 | C0340978 | May-Hegglin anomaly | 6 | UNIPROT |
Hgene | MYH9 | C0022661 | Kidney Failure, Chronic | 2 | CTD_human |
Hgene | MYH9 | C1854520 | SEBASTIAN SYNDROME | 2 | CTD_human;ORPHANET;UNIPROT |
Hgene | MYH9 | C0017668 | Focal glomerulosclerosis | 1 | CTD_human |
Hgene | MYH9 | C0020544 | Renal hypertension | 1 | CTD_human |
Hgene | MYH9 | C0027706 | Hereditary nephritis | 1 | CTD_human |
Hgene | MYH9 | C0036341 | Schizophrenia | 1 | PSYGENET |
Hgene | MYH9 | C1863659 | DEAFNESS, AUTOSOMAL DOMINANT 17 | 1 | UNIPROT |
Hgene | MYH9 | C2673482 | Increased susceptibility to schizophrenia | 1 | PSYGENET |
Tgene | NCL | C0151744 | Myocardial Ischemia | 1 | CTD_human |