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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:LARP7-ALPK1 (FusionGDB2 ID:43921)

Fusion Gene Summary for LARP7-ALPK1

check button Fusion gene summary
Fusion gene informationFusion gene name: LARP7-ALPK1
Fusion gene ID: 43921
HgeneTgene
Gene symbol

LARP7

ALPK1

Gene ID

51574

80216

Gene nameLa ribonucleoprotein 7, transcriptional regulatoralpha kinase 1
SynonymsALAZS|HDCMA18P|PIP7S8430410J10Rik|LAK
Cytomap

4q25

4q25

Type of geneprotein-codingprotein-coding
Descriptionla-related protein 7La ribonucleoprotein domain family member 7P-TEFb-interaction protein for 7SK stabilityalpha-protein kinase 1chromosome 4 kinaselymphocyte alpha-kinaselymphocyte alpha-protein kinase
Modification date2020031320200320
UniProtAcc

Q4G0J3

Q96QP1

Ensembl transtripts involved in fusion geneENST00000344442, ENST00000509061, 
ENST00000324052, ENST00000503898, 
ENST00000458497, ENST00000177648, 
ENST00000504176, ENST00000505912, 
Fusion gene scores* DoF score2 X 2 X 2=83 X 5 X 4=60
# samples 25
** MAII scorelog2(2/8*10)=1.32192809488736log2(5/60*10)=-0.263034405833794
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: LARP7 [Title/Abstract] AND ALPK1 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpointALPK1(113245232)-LARP7(113560614), # samples:2
LARP7(113558759)-ALPK1(113332983), # samples:2
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
TgeneALPK1

GO:0002753

cytoplasmic pattern recognition receptor signaling pathway

28222186|28877472|30111836

TgeneALPK1

GO:0043123

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

28222186|28877472|30111836

TgeneALPK1

GO:0045087

innate immune response

28222186|28877472|30111836


check buttonFusion gene breakpoints across LARP7 (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 ALPK1 (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
ChimerDB4BRCATCGA-A8-A09N-01ALARP7chr4

113558759

+ALPK1chr4

113332983

+
ChimerDB4BRCATCGA-A8-A09N-01ALARP7chr4

113558759

+ALPK1chr4

113332983

+


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Fusion Gene ORF analysis for LARP7-ALPK1

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-3CDSENST00000344442ENST00000458497LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3CDSENST00000344442ENST00000177648LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3CDSENST00000344442ENST00000504176LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3UTRENST00000344442ENST00000505912LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3CDSENST00000509061ENST00000458497LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3CDSENST00000509061ENST00000177648LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3CDSENST00000509061ENST00000504176LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3UTRENST00000509061ENST00000505912LARP7chr4

113558759

+ALPK1chr4

113332983

+
5UTR-3CDSENST00000324052ENST00000458497LARP7chr4

113558759

+ALPK1chr4

113332983

+
5UTR-3CDSENST00000324052ENST00000177648LARP7chr4

113558759

+ALPK1chr4

113332983

+
5UTR-3CDSENST00000324052ENST00000504176LARP7chr4

113558759

+ALPK1chr4

113332983

+
5UTR-3UTRENST00000324052ENST00000505912LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3CDSENST00000503898ENST00000458497LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3CDSENST00000503898ENST00000177648LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3CDSENST00000503898ENST00000504176LARP7chr4

113558759

+ALPK1chr4

113332983

+
intron-3UTRENST00000503898ENST00000505912LARP7chr4

113558759

+ALPK1chr4

113332983

+

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 LARP7-ALPK1


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)
LARP7chr4113558759+ALPK1chr4113332982+3.38E-060.99999666
LARP7chr4113558759+ALPK1chr4113332982+3.38E-060.99999666

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 LARP7-ALPK1


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
LARP7

Q4G0J3

ALPK1

Q96QP1

FUNCTION: RNA-binding protein that specifically binds distinct small nuclear RNA (snRNAs) and regulates their processing and function (PubMed:18249148, PubMed:32017898). Specifically binds the 7SK snRNA (7SK RNA) and acts as a core component of the 7SK ribonucleoprotein (RNP) complex, thereby acting as a negative regulator of transcription elongation by RNA polymerase II (PubMed:18249148, PubMed:18483487). The 7SK RNP complex sequesters the positive transcription elongation factor b (P-TEFb) in a large inactive 7SK RNP complex preventing RNA polymerase II phosphorylation and subsequent transcriptional elongation (PubMed:18249148, PubMed:18483487). The 7SK RNP complex also promotes snRNA gene transcription by RNA polymerase II via interaction with the little elongation complex (LEC) (PubMed:28254838). LARP7 specifically binds to the highly conserved 3'-terminal U-rich stretch of 7SK RNA; on stimulation, remains associated with 7SK RNA, whereas P-TEFb is released from the complex (PubMed:18483487, PubMed:18281698). LARP7 also acts as a regulator of mRNA splicing fidelity by promoting U6 snRNA processing (PubMed:32017898). Specifically binds U6 snRNAs and associates with a subset of box C/D RNP complexes: promotes U6 snRNA 2'-O-methylation by facilitating U6 snRNA loading into box C/D RNP complexes (PubMed:32017898). U6 snRNA 2'-O-methylation is required for mRNA splicing fidelity (PubMed:32017898). Binds U6 snRNAs with a 5'-CAGGG-3' sequence motif (PubMed:32017898). U6 snRNA processing is required for spermatogenesis (By similarity). {ECO:0000250|UniProtKB:Q05CL8, ECO:0000269|PubMed:18249148, ECO:0000269|PubMed:18281698, ECO:0000269|PubMed:18483487, ECO:0000269|PubMed:28254838, ECO:0000269|PubMed:32017898}.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}.

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 LARP7-ALPK1


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 LARP7-ALPK1


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 LARP7-ALPK1


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 LARP7-ALPK1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneLARP7C3554439Microcephalic primordial dwarfism Alazami type3CTD_human;GENOMICS_ENGLAND;ORPHANET
HgeneLARP7C0013336Dwarfism1GENOMICS_ENGLAND
HgeneLARP7C0020796Profound Mental Retardation1CTD_human
HgeneLARP7C0025363Mental Retardation, Psychosocial1CTD_human
HgeneLARP7C0342573PITUITARY DWARFISM I1GENOMICS_ENGLAND
HgeneLARP7C0917816Mental deficiency1CTD_human
HgeneLARP7C3714756Intellectual Disability1CTD_human
TgeneALPK1C0011849Diabetes Mellitus1CTD_human
TgeneALPK1C0011881Diabetic Nephropathy1CTD_human
TgeneALPK1C0017667Nodular glomerulosclerosis1CTD_human
TgeneALPK1C0018099Gout1CTD_human
TgeneALPK1C0027719Nephrosclerosis1CTD_human
TgeneALPK1C1262477Weight decreased1CTD_human