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Fusion gene ID: 653 |
FusionGeneSummary for ACVR1_NFATC1 |
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Fusion gene information | Fusion gene name: ACVR1_NFATC1 | Fusion gene ID: 653 | Hgene | Tgene | Gene symbol | ACVR1 | NFATC1 | Gene ID | 90 | 4772 |
Gene name | activin A receptor type 1 | nuclear factor of activated T cells 1 | |
Synonyms | ACTRI|ACVR1A|ACVRLK2|ALK2|FOP|SKR1|TSRI | NF-ATC|NF-ATc1.2|NFAT2|NFATc | |
Cytomap | 2q24.1 | 18q23 | |
Type of gene | protein-coding | protein-coding | |
Description | activin receptor type-1TGF-B superfamily receptor type Iactivin A receptor, type Iactivin A receptor, type II-like kinase 2activin receptor type Iactivin receptor-like kinase 2hydroxyalkyl-protein kinaseserine/threonine-protein kinase receptor R1 | nuclear factor of activated T-cells, cytoplasmic 1NFAT transcription complex cytosolic componentnuclear factor of activated T-cells 'c'nuclear factor of activated T-cells, cytoplasmic, calcineurin-dependent 1 | |
Modification date | 20180523 | 20180527 | |
UniProtAcc | Q04771 | O95644 | |
Ensembl transtripts involved in fusion gene | ENST00000263640, ENST00000409283, ENST00000434821, ENST00000410057, ENST00000487456, | ENST00000253506, ENST00000591814, ENST00000397790, ENST00000587635, ENST00000427363, ENST00000542384, ENST00000318065, ENST00000545796, ENST00000592223, ENST00000329101, ENST00000586434, ENST00000590172, | |
Fusion gene scores | * DoF score | 5 X 4 X 5=100 | 6 X 6 X 5=180 |
# samples | 7 | 8 | |
** MAII score | log2(7/100*10)=-0.514573172829758 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | log2(8/180*10)=-1.16992500144231 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ACVR1 [Title/Abstract] AND NFATC1 [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 | ACVR1 | GO:0006468 | protein phosphorylation | 12065756|19506109 |
Hgene | ACVR1 | GO:0007179 | transforming growth factor beta receptor signaling pathway | 8242742 |
Hgene | ACVR1 | GO:0010862 | positive regulation of pathway-restricted SMAD protein phosphorylation | 19506109 |
Hgene | ACVR1 | GO:0018107 | peptidyl-threonine phosphorylation | 19736306 |
Hgene | ACVR1 | GO:0030509 | BMP signaling pathway | 18436533 |
Hgene | ACVR1 | GO:0032924 | activin receptor signaling pathway | 19506109 |
Hgene | ACVR1 | GO:0045893 | positive regulation of transcription, DNA-templated | 8242742 |
Hgene | ACVR1 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 19506109 |
Hgene | ACVR1 | GO:0060389 | pathway-restricted SMAD protein phosphorylation | 19736306 |
Hgene | ACVR1 | GO:2000017 | positive regulation of determination of dorsal identity | 19506109 |
Tgene | NFATC1 | GO:0033173 | calcineurin-NFAT signaling cascade | 14979875 |
Tgene | NFATC1 | GO:0035556 | intracellular signal transduction | 14749367 |
Tgene | NFATC1 | GO:0045893 | positive regulation of transcription, DNA-templated | 14749367|14979875 |
Tgene | NFATC1 | GO:0045944 | positive regulation of transcription by RNA polymerase II | 14979875 |
Tgene | NFATC1 | GO:1905064 | negative regulation of vascular smooth muscle cell differentiation | 23853098 |
![]() (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 |
TCGA | RV | OV | TCGA-24-2281-01A | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
TCGA | LD | OV | TCGA-31-1946-01A | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
* 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 |
5UTR-3CDS | ENST00000263640 | ENST00000253506 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000591814 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000397790 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000587635 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000427363 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000542384 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000318065 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000545796 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000592223 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000329101 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000586434 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000263640 | ENST00000590172 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-3CDS | ENST00000409283 | ENST00000253506 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000591814 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000397790 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000587635 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000427363 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000542384 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000318065 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000545796 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000592223 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000329101 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000586434 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000409283 | ENST00000590172 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-3CDS | ENST00000434821 | ENST00000253506 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000591814 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000397790 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000587635 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000427363 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000542384 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000318065 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000545796 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000592223 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000329101 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000586434 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000434821 | ENST00000590172 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-3CDS | ENST00000410057 | ENST00000253506 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000591814 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000397790 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000587635 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000427363 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000542384 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000318065 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000545796 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000592223 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000329101 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000586434 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
5UTR-intron | ENST00000410057 | ENST00000590172 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-3CDS | ENST00000487456 | ENST00000253506 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000591814 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000397790 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000587635 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000427363 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000542384 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000318065 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000545796 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000592223 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000329101 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000586434 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
intron-intron | ENST00000487456 | ENST00000590172 | ACVR1 | chr2 | 158674897 | - | NFATC1 | chr18 | 77246248 | + |
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FusionProtFeatures for ACVR1_NFATC1 |
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Hgene | Tgene |
ACVR1 | NFATC1 |
On ligand binding, forms a receptor complex consistingof two type II and two type I transmembrane serine/threoninekinases. Type II receptors phosphorylate and activate type Ireceptors which autophosphorylate, then bind and activate SMADtranscriptional regulators. Receptor for activin. May be involvedfor left-right pattern formation during embryogenesis (Bysimilarity). {ECO:0000250}. |
![]() * 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 ACVR1_NFATC1 |
![]() (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 ACVR1_NFATC1 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
ACVR1 | FNTA, BMPR2, GDF5, ENG, BMP7, SMAD5, SMAD1, ACVR1B, TGFBR2, TSC22D1, IGSF1, SMURF1, BAMBI, SMAD6, SMAD7, PEG10, INHBA, ACVR2A, BMPR1A, ACVR1, USP15, ACVRL1, TGFBRAP1, GRAMD1A, MED16, RNF149, ARV1, OTUB1, LRRIQ1, TNFRSF10A, MRAP2, CD320 | NFATC1 | EGR1, EGR2, PIM1, HDAC3, PARP1, FOXP3, HDAC5, KAT2B, EP300, TUBA1A, KPNB1, HNRNPA1, UBE2I, PIAS1, HDAC2, HDAC1, HDAC4, RPS6KA3, RPS6KB1, GZF1, PML, OGT, YWHAQ, PPP3CC, FOS, JUN, HOXD13, CREB1, HIST1H2BA, HIST1H2BC, HIST3H3, ATF3, TP53, CHD4, ZMYM3, ISL1, SMARCA5, ADNP, CUX1, HIST1H2AD, RECQL, ATF1, FLYWCH1, GATAD2B, HMGA1, SMC3, ATF2, BEND3, KIF4A, LRWD1, SMC2, FRMPD1, HMGA2, HOXA10, JUND, ORC2, ORC5, PDS5A, PRDM15, SMARCA4, SMARCB1, SMARCC2, TAF10, TRPS1, ANKRD20A1, RBPJ, TEAD2, RPTOR, SCAI, GSK3B, WDR48, IKZF2, CHEK1, IKZF1, SATB1, RUNX1, CSNK1D, TRMT61B, MOSPD2, RFC5, NEK7, NEK6, FOXK2, PHGDH, JUNB, CREBBP, MTHFD2, LRRC47, NFATC2, FXR1, ACAD9, ZBTB40, RANBP9, DPF2, SMARCD2, LEF1, RFC2, VAPA, ATF7, SMARCE1, IFI16, CHAMP1, MDH2, XRCC6, HLTF, DNAJC7, MTHFD1L, CBFB, XRCC5, ACTL6A, RPA1, CTBP1, SMARCC1, HSPA5, RFC4, FOXK1, HSPA9, SMARCD1, ARID1A, LIG3, TUFM, NUP210, SARS2, BCL11B, TRRAP, CSNK1A1, CSNK1A1L, CAD, HMGCS2, PLOD1, PPP3R1, OBSL1, DNAAF2, SEMA7A, ZMYND19, MKLN1, LRRC28, ARMC8, PPP3CA |
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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 ACVR1_NFATC1 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Tgene | NFATC1 | O95644 | DB00852 | Pseudoephedrine | Nuclear factor of activated T-cells, cytoplasmic 1 | small molecule | approved |
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RelatedDiseases for ACVR1_NFATC1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ACVR1 | C0017638 | Glioma | 3 | CTD_human |
Hgene | ACVR1 | C0016037 | Fibrodysplasia Ossificans Progressiva | 2 | ORPHANET;UNIPROT |
Hgene | ACVR1 | C0004114 | Astrocytoma | 1 | CTD_human |
Hgene | ACVR1 | C0242488 | Acute Lung Injury | 1 | CTD_human |
Hgene | ACVR1 | C1458155 | Mammary Neoplasms | 1 | CTD_human |