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Fusion gene ID: 3307 |
FusionGeneSummary for ATP1A2_CPB1 |
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Fusion gene information | Fusion gene name: ATP1A2_CPB1 | Fusion gene ID: 3307 | Hgene | Tgene | Gene symbol | ATP1A2 | CPB1 | Gene ID | 477 | 1360 |
Gene name | ATPase Na+/K+ transporting subunit alpha 2 | carboxypeptidase B1 | |
Synonyms | FHM2|MHP2 | CPB|PASP|PCPB | |
Cytomap | 1q23.2 | 3q24 | |
Type of gene | protein-coding | protein-coding | |
Description | sodium/potassium-transporting ATPase subunit alpha-2ATPase Na+/K+ transporting alpha 2 polypeptideNa(+)/K(+) ATPase alpha-2 subunitNa+/K+ ATPase, alpha-A(+) catalytic polypeptideNa+/K+ ATPase, alpha-B polypeptidesodium pump subunit alpha-2sodium-pot | carboxypeptidase Bcarboxypeptidase B1 (tissue)pancreas-specific proteinpancreatic carboxypeptidase Bprocarboxypeptidase Bprotaminasetissue carboxypeptidase B | |
Modification date | 20180523 | 20180523 | |
UniProtAcc | P50993 | P15086 | |
Ensembl transtripts involved in fusion gene | ENST00000361216, ENST00000392233, ENST00000459972, | ENST00000491148, ENST00000282957, ENST00000498639, | |
Fusion gene scores | * DoF score | 2 X 2 X 2=8 | 21 X 24 X 3=1512 |
# samples | 2 | 19 | |
** MAII score | log2(2/8*10)=1.32192809488736 | log2(19/1512*10)=-2.99238681589013 possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs). DoF>8 and MAII<0 | |
Context | PubMed: ATP1A2 [Title/Abstract] AND CPB1 [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 | ATP1A2 | GO:0006883 | cellular sodium ion homeostasis | 10636900 |
Hgene | ATP1A2 | GO:0010107 | potassium ion import | 10636900 |
Hgene | ATP1A2 | GO:0030007 | cellular potassium ion homeostasis | 10636900 |
Hgene | ATP1A2 | GO:0036376 | sodium ion export across plasma membrane | 10636900 |
Hgene | ATP1A2 | GO:0071383 | cellular response to steroid hormone stimulus | 14742675 |
![]() (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 | LD | BRCA | TCGA-AN-A041-01A | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
* 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 |
3UTR-3CDS | ENST00000361216 | ENST00000491148 | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
3UTR-3CDS | ENST00000361216 | ENST00000282957 | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
3UTR-intron | ENST00000361216 | ENST00000498639 | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
intron-3CDS | ENST00000392233 | ENST00000491148 | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
intron-3CDS | ENST00000392233 | ENST00000282957 | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
intron-intron | ENST00000392233 | ENST00000498639 | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
intron-3CDS | ENST00000459972 | ENST00000491148 | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
intron-3CDS | ENST00000459972 | ENST00000282957 | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
intron-intron | ENST00000459972 | ENST00000498639 | ATP1A2 | chr1 | 160112554 | + | CPB1 | chr3 | 148562275 | + |
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FusionProtFeatures for ATP1A2_CPB1 |
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Hgene | Tgene |
ATP1A2 | CPB1 |
This is the catalytic component of the active enzyme,which catalyzes the hydrolysis of ATP coupled with the exchange ofsodium and potassium ions across the plasma membrane. This actioncreates the electrochemical gradient of sodium and potassium,providing the energy for active transport of various nutrients. |
![]() * 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 ATP1A2_CPB1 |
![]() (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 ATP1A2_CPB1 |
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Hgene | Hgene's interactors | Tgene | Tgene's interactors |
ATP1A2 | FBXO25, ZNRF2, ZNRF1, CUL3, CAND1, LGR4, ROGDI, P2RY8, CLTC, RAB1A, ATP6V0D1, ATP6V1A, CCT7, VDAC1, VDAC2, SCLT1, DOCK5, HIST1H4A, ARHGEF16 | CPB1 |
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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 ATP1A2_CPB1 |
![]() (DrugBank Version 5.1.0 2018-04-02) |
Partner | Gene | UniProtAcc | DrugBank ID | Drug name | Drug activity | Drug type | Drug status |
Hgene | ATP1A2 | P50993 | DB01092 | Ouabain | Sodium/potassium-transporting ATPase subunit alpha-2 | small molecule | approved |
Tgene | CPB1 | P15086 | DB04272 | Citric Acid | Carboxypeptidase B | small molecule | approved|nutraceutical|vet_approved |
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RelatedDiseases for ATP1A2_CPB1 |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |
Hgene | ATP1A2 | C1865322 | MIGRAINE, FAMILIAL HEMIPLEGIC, 2 | 6 | CTD_human;UNIPROT |
Hgene | ATP1A2 | C0020538 | Hypertensive disease | 2 | CTD_human |
Hgene | ATP1A2 | C0005586 | Bipolar Disorder | 1 | PSYGENET |
Hgene | ATP1A2 | C3549447 | ALTERNATING HEMIPLEGIA OF CHILDHOOD 1 | 1 | UNIPROT |