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Center for Computational Systems Medicine
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Fusion Gene Summary

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Fusion Gene ORF analysis

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Fusion Genomic Features

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Fusion Protein Features

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Fusion Gene Sequence

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Fusion Gene PPI analysis

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Related Drugs

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Related Diseases

Fusion gene:ALPK1-ELP2 (FusionGDB2 ID:4210)

Fusion Gene Summary for ALPK1-ELP2

check button Fusion gene summary
Fusion gene informationFusion gene name: ALPK1-ELP2
Fusion gene ID: 4210
HgeneTgene
Gene symbol

ALPK1

ELP2

Gene ID

80216

55250

Gene namealpha kinase 1elongator acetyltransferase complex subunit 2
Synonyms8430410J10Rik|LAKMRT58|SHINC-2|STATIP1|StIP
Cytomap

4q25

18q12.2

Type of geneprotein-codingprotein-coding
Descriptionalpha-protein kinase 1chromosome 4 kinaselymphocyte alpha-kinaselymphocyte alpha-protein kinaseelongator complex protein 2STAT3-interacting protein 1elongation protein 2 homologelongator protein 2signal transducer and activator of transcription 3 interacting protein 1
Modification date2020032020200313
UniProtAcc

Q96QP1

Q6IA86

Ensembl transtripts involved in fusion geneENST00000458497, ENST00000177648, 
ENST00000504176, ENST00000505912, 
ENST00000358232, ENST00000351393, 
ENST00000442325, ENST00000423854, 
ENST00000350494, ENST00000542824, 
ENST00000542050, 
Fusion gene scores* DoF score6 X 6 X 3=1086 X 12 X 5=360
# samples 611
** MAII scorelog2(6/108*10)=-0.84799690655495
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(11/360*10)=-1.71049338280502
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: ALPK1 [Title/Abstract] AND ELP2 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointALPK1(113252491)-ELP2(33739945), # samples:1
Anticipated loss of major functional domain due to fusion event.
* DoF score (Degree of Frequency) = # partners X # break points X # cancer types
** MAII score (Major Active Isofusion Index) = log2(# samples/DoF score*10)

check button Gene ontology of each fusion partner gene with evidence of Inferred from Direct Assay (IDA) from Entrez
PartnerGeneGO IDGO termPubMed ID
HgeneALPK1

GO:0002753

cytoplasmic pattern recognition receptor signaling pathway

28222186|28877472|30111836

HgeneALPK1

GO:0043123

positive regulation of I-kappaB kinase/NF-kappaB signaling

28222186|28877472|30111836

HgeneALPK1

GO:0045087

innate immune response

28222186|28877472|30111836


check buttonFusion gene breakpoints across ALPK1 (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check buttonFusion gene breakpoints across ELP2 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.

check button Fusion gene information from two resources (ChiTars 5.0 and ChimerDB 4.0)
* 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.
SourceDiseaseSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS5.0N/ABQ359089ALPK1chr4

113252491

+ELP2chr18

33739945

-


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Fusion Gene ORF analysis for ALPK1-ELP2

check button Open reading frame (ORF) analsis of fusion genes based on Ensembl gene isoform structure.
* Click on the break point to see the gene structure around the break point region using the UCSC Genome Browser.
ORFHenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrand
intron-3CDSENST00000458497ENST00000358232ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000458497ENST00000351393ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000458497ENST00000442325ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000458497ENST00000423854ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000458497ENST00000350494ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000458497ENST00000542824ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-intronENST00000458497ENST00000542050ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000177648ENST00000358232ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000177648ENST00000351393ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000177648ENST00000442325ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000177648ENST00000423854ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000177648ENST00000350494ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000177648ENST00000542824ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-intronENST00000177648ENST00000542050ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000504176ENST00000358232ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000504176ENST00000351393ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000504176ENST00000442325ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000504176ENST00000423854ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000504176ENST00000350494ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000504176ENST00000542824ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-intronENST00000504176ENST00000542050ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000505912ENST00000358232ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000505912ENST00000351393ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000505912ENST00000442325ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000505912ENST00000423854ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000505912ENST00000350494ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-3CDSENST00000505912ENST00000542824ALPK1chr4

113252491

+ELP2chr18

33739945

-
intron-intronENST00000505912ENST00000542050ALPK1chr4

113252491

+ELP2chr18

33739945

-

check buttonORFfinder result based on the fusion transcript sequence of in-frame fusion genes.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)

check buttonDeepORF prediction of the coding potential based on the fusion transcript sequence of in-frame fusion genes. DeepORF is a coding potential classifier based on convolutional neural network by comparing the real Ribo-seq data. If the no-coding score < 0.5 and coding score > 0.5, then the in-frame fusion transcript is predicted as being likely translated.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandNo-coding scoreCoding score

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Fusion Genomic Features for ALPK1-ELP2


check buttonFusionAI prediction of the potential fusion gene breakpoint based on the pre-mature RNA sequence context (+/- 5kb of individual partner genes, total 20kb length sequence). FusionAI is a fusion gene breakpoint classifier based on convolutional neural network by comparing the fusion positive and negative sequence context of ~ 20K fusion gene data. From here, we can have the relative potentency of the 20K genomic sequence how individual sequnce will be likely used as the gene fusion breakpoints.
HgeneHchrHbpHstrandTgeneTchrTbpTstrand1-pp (fusion gene breakpoint)

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions. We integrated a total of 44 different types of human genomic feature loci information across five big categories including virus integration sites, repeats, structural variants, chromatin states, and gene expression regulation. More details are in help page.

check buttonDistribution of 44 human genomic features loci across 20kb length fusion breakpoint regions that are ovelapped with the top 1% feature importance score regions. More details are in help page.

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Fusion Protein Features for ALPK1-ELP2


check button Go to

FGviewer for the breakpoints of :-:

.
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
FGviewer

check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
ALPK1

Q96QP1

ELP2

Q6IA86

FUNCTION: Serine/threonine-protein kinase that detects bacterial pathogen-associated molecular pattern metabolites (PAMPs) and initiates an innate immune response, a critical step for pathogen elimination and engagement of adaptive immunity (PubMed:28877472, PubMed:28222186, PubMed:30111836). Specifically recognizes and binds ADP-D-glycero-beta-D-manno-heptose (ADP-Heptose), a potent PAMP present in all Gram-negative and some Gram-positive bacteria (PubMed:30111836). ADP-Heptose-binding stimulates its kinase activity to phosphorylate and activate TIFA, triggering proinflammatory NF-kappa-B signaling (PubMed:30111836). May be involved in monosodium urate monohydrate (MSU)-induced inflammation by mediating phosphorylation of unconventional myosin MYO9A (PubMed:27169898). May also play a role in apical protein transport by mediating phosphorylation of unconventional myosin MYO1A (PubMed:15883161). {ECO:0000269|PubMed:15883161, ECO:0000269|PubMed:27169898, ECO:0000269|PubMed:28222186, ECO:0000269|PubMed:28877472, ECO:0000269|PubMed:30111836}.FUNCTION: Component of the RNA polymerase II elongator complex, a multiprotein complex associated with the RNA polymerase II (Pol II) holoenzyme, and which is involved in transcriptional elongation (PubMed:11714725, PubMed:11818576). The elongator complex catalyzes formation of carboxymethyluridine in the wobble base at position 34 in tRNAs (PubMed:29332244). {ECO:0000269|PubMed:11714725, ECO:0000269|PubMed:11818576, ECO:0000303|PubMed:29332244}.

check buttonRetention analysis result of each fusion partner protein across 39 protein features of UniProt such as six molecule processing features, 13 region features, four site features, six amino acid modification features, two natural variation features, five experimental info features, and 3 secondary structure features. Here, because of limited space for viewing, we only show the protein feature retention information belong to the 13 regional features. All retention annotation result can be downloaded at

download page


* 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.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note

- In-frame and not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note


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Fusion Gene Sequence for ALPK1-ELP2


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences. To have fusion amino acid sequence, we ran ORFfinder and chose the longest ORF among the all predicted ones.

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Fusion Gene PPI Analysis for ALPK1-ELP2


check button Go to ChiPPI (Chimeric Protein-Protein interactions) to see the chimeric PPI interaction in

ChiPPI page.


check button Protein-protein interactors with each fusion partner protein in wild-type (BIOGRID-3.4.160)
HgeneHgene's interactorsTgeneTgene's interactors


check button - Retained PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost PPIs in in-frame fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


check button - Retained PPIs, but lost function due to frame-shift fusion.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs for ALPK1-ELP2


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.8 2021-05-08)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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Related Diseases for ALPK1-ELP2


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneALPK1C0011849Diabetes Mellitus1CTD_human
HgeneALPK1C0011881Diabetic Nephropathy1CTD_human
HgeneALPK1C0017667Nodular glomerulosclerosis1CTD_human
HgeneALPK1C0018099Gout1CTD_human
HgeneALPK1C0027719Nephrosclerosis1CTD_human
HgeneALPK1C1262477Weight decreased1CTD_human
TgeneELP2C0020796Profound Mental Retardation1CTD_human
TgeneELP2C0025363Mental Retardation, Psychosocial1CTD_human
TgeneELP2C0917816Mental deficiency1CTD_human
TgeneELP2C3714756Intellectual Disability1CTD_human
TgeneELP2C4310641MENTAL RETARDATION, AUTOSOMAL RECESSIVE 581CTD_human;GENOMICS_ENGLAND;UNIPROT