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Fusion Protein:HCN2-ALS2CR11 |
Fusion Protein Summary |
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Fusion partner gene information | Fusion gene name: HCN2-ALS2CR11 | FusionPDB ID: 35781 | FusionGDB2.0 ID: 35781 | Hgene | Tgene | Gene symbol | HCN2 | ALS2CR11 | Gene ID | 610 | 151254 |
Gene name | hyperpolarization activated cyclic nucleotide gated potassium and sodium channel 2 | C2 calcium dependent domain containing 6 | |
Synonyms | BCNG-2|BCNG2|HAC-1 | ALS2CR11 | |
Cytomap | 19p13.3 | 2q33.1 | |
Type of gene | protein-coding | protein-coding | |
Description | potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2brain cyclic nucleotide-gated channel 2hyperpolarization activated cyclic nucleotide gated potassium channel 2 | C2 calcium-dependent domain-containing protein 6amyotrophic lateral sclerosis 2 (juvenile) chromosome region, candidate 11amyotrophic lateral sclerosis 2 chromosomal region candidate gene 11 proteinamyotrophic lateral sclerosis 2 chromosome region cand | |
Modification date | 20200313 | 20200313 | |
UniProtAcc | Q9UL51 | . | |
Ensembl transtripts involved in fusion gene | ENST ids | ENST00000251287, | ENST00000450242, ENST00000482942, ENST00000286195, ENST00000439140, ENST00000439802, |
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0) | * DoF score | 2 X 1 X 2=4 | 3 X 4 X 3=36 |
# samples | 2 | 4 | |
** MAII score | log2(2/4*10)=2.32192809488736 | log2(4/36*10)=0.15200309344505 effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs). DoF>8 and MAII>0 | |
Context (manual curation of fusion genes in FusionPDB) | PubMed: HCN2 [Title/Abstract] AND ALS2CR11 [Title/Abstract] AND fusion [Title/Abstract] | ||
Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0) | HCN2(590577)-ALS2CR11(202412333), # samples:2 | ||
Anticipated loss of major functional domain due to fusion event. | HCN2-ALS2CR11 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. HCN2-ALS2CR11 seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF. HCN2-ALS2CR11 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. HCN2-ALS2CR11 seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF. |
* 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 | HCN2 | GO:0071320 | cellular response to cAMP | 10228147|22748890 |
Hgene | HCN2 | GO:0071321 | cellular response to cGMP | 22748890 |
Hgene | HCN2 | GO:0071805 | potassium ion transmembrane transport | 10228147 |
Hgene | HCN2 | GO:0098719 | sodium ion import across plasma membrane | 10228147 |
Hgene | HCN2 | GO:1990573 | potassium ion import across plasma membrane | 10228147 |
![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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![]() * Click on the image to open the UCSC genome browser with custom track showing this image in a new window. |
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Fusion Gene Sample Information |
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![]() * 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. |
Source | Disease | Sample | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand |
ChimerDB4 | CESC | TCGA-C5-A2LZ-01A | HCN2 | chr19 | 590577 | - | ALS2CR11 | chr2 | 202412333 | - |
ChimerDB4 | CESC | TCGA-C5-A2LZ-01A | HCN2 | chr19 | 590577 | + | ALS2CR11 | chr2 | 202412333 | - |
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Fusion ORF Analysis |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | Seq length (transcript) | BP loci (transcript) | Predicted start (transcript) | Predicted stop (transcript) | Seq length (amino acids) |
ENST00000251287 | HCN2 | chr19 | 590577 | + | ENST00000286195 | ALS2CR11 | chr2 | 202412333 | - | 1767 | 685 | 53 | 1579 | 508 |
ENST00000251287 | HCN2 | chr19 | 590577 | + | ENST00000439802 | ALS2CR11 | chr2 | 202412333 | - | 1323 | 685 | 53 | 895 | 280 |
ENST00000251287 | HCN2 | chr19 | 590577 | + | ENST00000439140 | ALS2CR11 | chr2 | 202412333 | - | 5175 | 685 | 53 | 5170 | 1705 |
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Henst | Tenst | Hgene | Hchr | Hbp | Hstrand | Tgene | Tchr | Tbp | Tstrand | No-coding score | Coding score |
ENST00000251287 | ENST00000286195 | HCN2 | chr19 | 590577 | + | ALS2CR11 | chr2 | 202412333 | - | 0.0045524 | 0.9954476 |
ENST00000251287 | ENST00000439802 | HCN2 | chr19 | 590577 | + | ALS2CR11 | chr2 | 202412333 | - | 0.027212005 | 0.97278804 |
ENST00000251287 | ENST00000439140 | HCN2 | chr19 | 590577 | + | ALS2CR11 | chr2 | 202412333 | - | 0.000229562 | 0.99977046 |
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Fusion Amino Acid Sequences |
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>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP >35781_35781_1_HCN2-ALS2CR11_HCN2_chr19_590577_ENST00000251287_ALS2CR11_chr2_202412333_ENST00000286195_length(amino acids)=508AA_BP=207 MDARGGGGRPGESPGATPAPGPPPPPPPAPPQQQPPPPPPPAPPPGPGPAPPQHPPRAEALPPEAADEGGPRGRLRSRDSSCGRPGTPGA ASTAKGSPNGECGRGEPQCSPAGPEGPARGPKVSFSCRGAASGPAPGPGPAEEAGSEEAGPAGEPRGSQASFMQRQFGALLQPGVNKFSL RMFGSQKAVEREQERVKSAGAWIIHPYSDFRLEKMKKEYRNLNTWIDKANYLESILMPKLEHKDSEETNIDEASENTKSNHPEEELENIV GVDIPLVNEEAETTANELLDNDSEKGLTIPTLNQSDQDNSTADASKNDESTPSPTEVHSLCTISNQETIKAGRIPPLGERQSESMPDRKM KNVFFPLEVKLKDNYPSILKADSSLSEVAFSPKEYNSPSFRPEYIEFKPKFQDCSDKFEDLHDMTSFTHLKKVKSRSRLLGKSSDDIHNH -------------------------------------------------------------- >35781_35781_2_HCN2-ALS2CR11_HCN2_chr19_590577_ENST00000251287_ALS2CR11_chr2_202412333_ENST00000439140_length(amino acids)=1705AA_BP=207 MDARGGGGRPGESPGATPAPGPPPPPPPAPPQQQPPPPPPPAPPPGPGPAPPQHPPRAEALPPEAADEGGPRGRLRSRDSSCGRPGTPGA ASTAKGSPNGECGRGEPQCSPAGPEGPARGPKVSFSCRGAASGPAPGPGPAEEAGSEEAGPAGEPRGSQASFMQRQFGALLQPGVNKFSL RMFGSQKAVEREQERVKSAGAWIIHPYSDFRLEKMKKEYRNLNTWIDKANYLESILMPKLEHKDSEETNIDEASENTKSNHPEEELENIV GVDIPLVNEEAETTANELLDNDSEKGLTIPTLNQSDQDNSTADASKNDESTPSPTEVHSLCTISNQETIKAGRIPPLGERQSESMPDRKM KNVFFPLEVKLKDNYPSILKADSSLSEVAFSPKEYNSPSFRPEYIEFKPKFQFQKFNKNGFDPFLRNINKMSVRKRKDQDIYKYRNILGA EVIEHEDQDPPYPAQSKTAGPANTTWAHDPNIFTTKMLETENKLAPDPTINTIKGLDTKNSLKENLPNVSLPSIKGESSRAGNVQANTCH LSKSLNFTPHIEYLKQSMILKSILSENLQDLSDKLFSKPEVSMNSEAREKSSSPLLSIHDKSSSSMEDNVLEKKQDLNNWLSEKDILNSK TTLSQIIKNIPADSFSEGSQIIENIPADSLLEGGQVIKNIPEYSLSEGGQIIKNIPADSFLESGPGQSPEVEEHVSKKHFEADERDFPIK KNSSTKKKHLISEVPNSKSGSSGTVHDYIMRQIFTAPIFSELEIEVKEPSETPMNLENQLPTPWKRSLSSHILFHEENADEIELPQPRSA TSQIIQAFPIDTLLESGIIKVIELDKEHHKSSLLGTGITSPKGNLKDSQEYYSEIRSETEPLSEQSIPIIPKDTTSVSRAEFIQEDQNMF PQDSSYYSIANKELYLPRNGQRLCKDKNDLSSTLESLTNSLMDKLSESDEIMLKSFLKNIFNVFFKYNHSERRGQPEKELERLIQPSFTS DTEHLEELQEDFDKADKLDRKPILSPKLRVFLEELSESEVKHLKSELSKQIQHYLVERLSESGHITKEDLPKIYQNLYLMNEKAEQKGPN SFQGKYSETVKEIMSFVNNFNHHFIDKHLEIKLRSFLKEILQNYFLKNISESSLFNETASETIYPNISSLRTKSVSISFHELEQDISKGS FGRRFEINMKYPLSKSLQNYLIALSENELLHLKADLSKHLQSLFIEKLSKSGLMTKKQLEGINQHINLLNSSSIPLKYIKTHLPFRDDCH FVEKHSEKQNKYSRIVQQTTLQTVSEDKLREAELIREKEKKYFPLQNLKGNSSLIKEQKSYYTKEEAKTPSLIKVQPSSNENIQASPLSK SSEILTDILLKKLRKEHVFTQLPQAENSVHKTEIQDPYSWGGKSKITQSKAWCEKTLKMKSLDRKEHVNIYKWTVQEKPEAVLTSYPRIP NARMPREDEYLNRITFPSWQSSTLTHFNTETGEKSKLEDQYCQTLKGNNNNNKKHLVTFAQYKKEIQTLYIKPDEICSEKCAKFPEIQSF QYKVVEDEKNLKPHLFPELFKIEDLKPKVRKERDRVAQPKKSFNKIVRILPTTLPTTRIHLKKSVPRTLLHWTARRTIHDCSDKFEDLHD -------------------------------------------------------------- >35781_35781_3_HCN2-ALS2CR11_HCN2_chr19_590577_ENST00000251287_ALS2CR11_chr2_202412333_ENST00000439802_length(amino acids)=280AA_BP=207 MDARGGGGRPGESPGATPAPGPPPPPPPAPPQQQPPPPPPPAPPPGPGPAPPQHPPRAEALPPEAADEGGPRGRLRSRDSSCGRPGTPGA ASTAKGSPNGECGRGEPQCSPAGPEGPARGPKVSFSCRGAASGPAPGPGPAEEAGSEEAGPAGEPRGSQASFMQRQFGALLQPGVNKFSL RMFGSQKAVEREQERVKSAGAWIIHPYSDFRLEKMKKEYRNLNTWIDKANYLESILMPKLEHKDSEETNIDEASENTKSNHPEEELENIV -------------------------------------------------------------- |
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Fusion Protein Functional Features |
![]() Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr19:590577/chr2:202412333) - FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels. - How to search 1. Put your fusion gene symbol. 2. Press the tab key until there will be shown the breakpoint information filled. 4. Go down and press 'Search' tab twice. 4. Go down to have the hyperlink of the search result. 5. Click the hyperlink. 6. See the FGviewer result for your fusion gene. |
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Hgene | Tgene |
HCN2 | . |
FUNCTION: Hyperpolarization-activated ion channel exhibiting weak selectivity for potassium over sodium ions. Contributes to the native pacemaker currents in heart (If) and in neurons (Ih). Can also transport ammonium in the distal nephron. Produces a large instantaneous current. Modulated by intracellular chloride ions and pH; acidic pH shifts the activation to more negative voltages (By similarity). {ECO:0000250, ECO:0000269|PubMed:10228147, ECO:0000269|PubMed:10524219}. | FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes. |
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- 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 |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 10_140 | 210.66666666666666 | 890.0 | Compositional bias | Note=Pro-rich |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 158_209 | 210.66666666666666 | 890.0 | Region | Involved in subunit assembly |
- 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 |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 715_861 | 210.66666666666666 | 890.0 | Compositional bias | Note=Pro-rich |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 414_435 | 210.66666666666666 | 890.0 | Intramembrane | Pore-forming%3B Name%3DSegment H5 |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 608_611 | 210.66666666666666 | 890.0 | Nucleotide binding | cAMP |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 618_619 | 210.66666666666666 | 890.0 | Nucleotide binding | cAMP |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 659_662 | 210.66666666666666 | 890.0 | Nucleotide binding | cAMP |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 1_215 | 210.66666666666666 | 890.0 | Topological domain | Cytoplasmic |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 237_240 | 210.66666666666666 | 890.0 | Topological domain | Extracellular |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 262_288 | 210.66666666666666 | 890.0 | Topological domain | Cytoplasmic |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 310_317 | 210.66666666666666 | 890.0 | Topological domain | Extracellular |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 339_369 | 210.66666666666666 | 890.0 | Topological domain | Cytoplasmic |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 391_413 | 210.66666666666666 | 890.0 | Topological domain | Extracellular |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 436_440 | 210.66666666666666 | 890.0 | Topological domain | Extracellular |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 462_889 | 210.66666666666666 | 890.0 | Topological domain | Cytoplasmic |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 216_236 | 210.66666666666666 | 890.0 | Transmembrane | Helical%3B Name%3DSegment S1 |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 241_261 | 210.66666666666666 | 890.0 | Transmembrane | Helical%3B Name%3DSegment S2 |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 289_309 | 210.66666666666666 | 890.0 | Transmembrane | Helical%3B Name%3DSegment S3 |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 318_338 | 210.66666666666666 | 890.0 | Transmembrane | Helical%3B Voltage-sensor%3B Name%3DSegment S4 |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 370_390 | 210.66666666666666 | 890.0 | Transmembrane | Helical%3B Name%3DSegment S5 |
Hgene | HCN2 | chr19:590577 | chr2:202412333 | ENST00000251287 | + | 1 | 8 | 441_461 | 210.66666666666666 | 890.0 | Transmembrane | Helical%3B Name%3DSegment S6 |
Tgene | ALS2CR11 | chr19:590577 | chr2:202412333 | ENST00000286195 | 8 | 15 | 87_222 | 325.6666666666667 | 624.0 | Domain | C2 | |
Tgene | ALS2CR11 | chr19:590577 | chr2:202412333 | ENST00000439140 | 8 | 16 | 87_222 | 325.6666666666667 | 1821.0 | Domain | C2 | |
Tgene | ALS2CR11 | chr19:590577 | chr2:202412333 | ENST00000439802 | 8 | 13 | 87_222 | 325.6666666666667 | 433.0 | Domain | C2 | |
Tgene | ALS2CR11 | chr19:590577 | chr2:202412333 | ENST00000450242 | 8 | 13 | 87_222 | 325.6666666666667 | 551.0 | Domain | C2 |
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Fusion Protein-Protein Interaction |
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Gene | PPI interactors |
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Gene | STRING network |
HCN2 | |
ALS2CR11 |
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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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Related Drugs to HCN2-ALS2CR11 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Drug | Source | PMID |
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Related Diseases to HCN2-ALS2CR11 |
![]() (Manual curation of PubMed, 04-30-2022 + MyCancerGenome) |
Hgene | Tgene | Disease | Source | PMID |
![]() (DisGeNet 4.0) |
Partner | Gene | Disease ID | Disease name | # pubmeds | Source |