![]() |
||||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Fusion gene ID: 34973 |
FusionGeneSummary for SMR3B_MYH9 |
![]() |
Fusion gene information | Fusion gene name: SMR3B_MYH9 | Fusion gene ID: 34973 | Hgene | Tgene | Gene symbol | SMR3B | MYH9 | Gene ID | 10879 | 4627 |
Gene name | submaxillary gland androgen regulated protein 3B | myosin heavy chain 9 | |
Synonyms | P-B|PBII|PRL3|PROL3|SMR1B | BDPLT6|DFNA17|EPSTS|FTNS|MHA|NMHC-II-A|NMMHC-IIA|NMMHCA | |
Cytomap | 4q13.3 | 22q12.3 | |
Type of gene | protein-coding | protein-coding | |
Description | submaxillary gland androgen-regulated protein 3Bproline rich 3proline-rich peptide P-Bproline-rich protein 3salivary proline-rich proteinsubmaxillary gland androgen regulated protein 3 homolog B | 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 | |
Modification date | 20180523 | 20180522 | |
UniProtAcc | P02814 | P35579 | |
Ensembl transtripts involved in fusion gene | ENST00000504825, ENST00000304915, | ENST00000216181, ENST00000475726, ENST00000401701, | |
Fusion gene scores | * DoF score | 2 X 2 X 1=4 | 23 X 25 X 7=4025 |
# samples | 2 | 28 | |
** MAII score | log2(2/4*10)=2.32192809488736 | log2(28/4025*10)=-3.84549005094438 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: SMR3B [Title/Abstract] AND MYH9 [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) |
![]() |
Partner | Gene | GO ID | GO term | PubMed ID |
Tgene | MYH9 | GO:0001525 | angiogenesis | 16403913 |
Tgene | MYH9 | GO:0006509 | membrane protein ectodomain proteolysis | 16186248 |
Tgene | MYH9 | GO:0030048 | actin filament-based movement | 12237319|15845534 |
Tgene | 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 | BX486673 | SMR3B | chr4 | 71255517 | + | MYH9 | chr22 | 36768443 | - |
* 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 |
5CDS-intron | ENST00000504825 | ENST00000216181 | SMR3B | chr4 | 71255517 | + | MYH9 | chr22 | 36768443 | - |
5CDS-intron | ENST00000504825 | ENST00000475726 | SMR3B | chr4 | 71255517 | + | MYH9 | chr22 | 36768443 | - |
5CDS-intron | ENST00000504825 | ENST00000401701 | SMR3B | chr4 | 71255517 | + | MYH9 | chr22 | 36768443 | - |
5CDS-intron | ENST00000304915 | ENST00000216181 | SMR3B | chr4 | 71255517 | + | MYH9 | chr22 | 36768443 | - |
5CDS-intron | ENST00000304915 | ENST00000475726 | SMR3B | chr4 | 71255517 | + | MYH9 | chr22 | 36768443 | - |
5CDS-intron | ENST00000304915 | ENST00000401701 | SMR3B | chr4 | 71255517 | + | MYH9 | chr22 | 36768443 | - |
Top |
FusionProtFeatures for SMR3B_MYH9 |
![]() |
Hgene | Tgene |
SMR3B | MYH9 |
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}. |
![]() * 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 |
Top |
FusionGeneSequence for SMR3B_MYH9 |
![]() (nt: nucleotides, aa: amino acids) |
* Fusion amino acid sequences. |
* Fusion transcript sequences (only coding sequence (CDS) region). |
* Fusion transcript sequences (Full-length transcript). |
Top |
FusionGenePPI for SMR3B_MYH9 |
![]() |
![]() |
Hgene | Hgene's interactors | Tgene | Tgene's interactors |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Still interaction with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
![]() |
Partner | Gene | Hbp | Tbp | ENST | Strand | BPexon | TotalExon | Protein feature loci | *BPloci | TotalLen | Interaction lost with |
Top |
RelatedDrugs for SMR3B_MYH9 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | MYH9 | P35579 | DB11638 | Artenimol | Myosin-9 | small molecule | approved|investigational |
Top |
RelatedDiseases for SMR3B_MYH9 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Tgene | MYH9 | C0403445 | Fechtner syndrome (disorder) | 9 | UNIPROT |
Tgene | MYH9 | C0398641 | Epstein syndrome (disorder) | 7 | UNIPROT |
Tgene | MYH9 | C0340978 | May-Hegglin anomaly | 6 | UNIPROT |
Tgene | MYH9 | C0022661 | Kidney Failure, Chronic | 2 | CTD_human |
Tgene | MYH9 | C1854520 | SEBASTIAN SYNDROME | 2 | CTD_human;ORPHANET;UNIPROT |
Tgene | MYH9 | C0017668 | Focal glomerulosclerosis | 1 | CTD_human |
Tgene | MYH9 | C0020544 | Renal hypertension | 1 | CTD_human |
Tgene | MYH9 | C0027706 | Hereditary nephritis | 1 | CTD_human |
Tgene | MYH9 | C0036341 | Schizophrenia | 1 | PSYGENET |
Tgene | MYH9 | C1863659 | DEAFNESS, AUTOSOMAL DOMINANT 17 | 1 | UNIPROT |
Tgene | MYH9 | C2673482 | Increased susceptibility to schizophrenia | 1 | PSYGENET |