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Center for Computational Systems Medicine
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FusionGeneSummary

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FusionProtFeature

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FusionGeneSequence

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FusionGenePPI

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RelatedDrugs

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RelatedDiseases

Fusion gene ID: 7364

FusionGeneSummary for CLEC16A_NBAS

check button Fusion gene summary
Fusion gene informationFusion gene name: CLEC16A_NBAS
Fusion gene ID: 7364
HgeneTgene
Gene symbol

CLEC16A

NBAS

Gene ID

23274

51594

Gene nameC-type lectin domain containing 16Aneuroblastoma amplified sequence
SynonymsGop-1|KIAA0350ILFS2|NAG|SOPH
Cytomap

16p13.13

2p24.3

Type of geneprotein-codingprotein-coding
Descriptionprotein CLEC16AC-type lectin domain family 16 member Aneuroblastoma-amplified sequenceNAG/BC035112 fusionNAG/FAM49A fusionneuroblastoma-amplified gene protein
Modification date2018052720180519
UniProtAcc

Q2KHT3

A2RRP1

Ensembl transtripts involved in fusion geneENST00000409790, ENST00000409552, 
ENST00000465491, ENST00000381822, 
ENST00000441750, ENST00000281513, 
Fusion gene scores* DoF score9 X 7 X 6=3788 X 9 X 3=216
# samples 129
** MAII scorelog2(12/378*10)=-1.65535182861255
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/216*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: CLEC16A [Title/Abstract] AND NBAS [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)

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

check button Fusion gene information from three resources
(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 typeSourceCancer typeSampleHgeneHchrHbpHstrandTgeneTchrTbpTstrand
ChiTaRS3.1BQ380493CLEC16Achr16

11102571

+NBASchr2

15315355

+
* LD: Li Ding group's fusion gene list
  RV: Roel Verhaak group's fusion gene list
  ChiTaRs fusion database

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-intronENST00000409790ENST00000441750CLEC16Achr16

11102571

+NBASchr2

15315355

+
intron-intronENST00000409790ENST00000281513CLEC16Achr16

11102571

+NBASchr2

15315355

+
intron-intronENST00000409552ENST00000441750CLEC16Achr16

11102571

+NBASchr2

15315355

+
intron-intronENST00000409552ENST00000281513CLEC16Achr16

11102571

+NBASchr2

15315355

+
intron-intronENST00000465491ENST00000441750CLEC16Achr16

11102571

+NBASchr2

15315355

+
intron-intronENST00000465491ENST00000281513CLEC16Achr16

11102571

+NBASchr2

15315355

+
intron-intronENST00000381822ENST00000441750CLEC16Achr16

11102571

+NBASchr2

15315355

+
intron-intronENST00000381822ENST00000281513CLEC16Achr16

11102571

+NBASchr2

15315355

+

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FusionProtFeatures for CLEC16A_NBAS


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
CLEC16A

Q2KHT3

NBAS

A2RRP1

Regulator of mitophagy through the upstream regulationof the RNF41/NRDP1-PRKN pathway. Mitophagy is a selective form ofautophagy necessary for mitochondrial quality control. TheRNF41/NRDP1-PRKN pathway regulates autophagosome-lysosome fusionduring late mitophagy. May protect RNF41/NRDP1 from proteosomaldegradation, RNF41/NRDP1 which regulates proteosomal degradationof PRKN. Plays a key role in beta cells functions by regulatingmitophagy/autophagy and mitochondrial health.{ECO:0000269|PubMed:24949970}. Involved in Golgi-to-endoplasmic reticulum (ER)retrograde transport; the function is proposed to depend on itsassociation in the NRZ complex which is believed to play a role inSNARE assembly at the ER (PubMed:19369418).{ECO:0000269|PubMed:19369418, ECO:0000305}.

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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FusionGeneSequence for CLEC16A_NBAS


check button For in-frame fusion transcripts, we provide the fusion transcript sequences and fusion amino acid sequences.
(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 CLEC16A_NBAS


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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RelatedDrugs for CLEC16A_NBAS


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status

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RelatedDiseases for CLEC16A_NBAS


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneCLEC16AC0011854Diabetes Mellitus, Insulin-Dependent2CTD_human
HgeneCLEC16AC0026769Multiple Sclerosis2CTD_human
HgeneCLEC16AC0162538Immunoglobulin A deficiency (disorder)2CTD_human
HgeneCLEC16AC0001403Addison Disease1CTD_human
HgeneCLEC16AC0023892Biliary cirrhosis1CTD_human
HgeneCLEC16AC0024141Lupus Erythematosus, Systemic1CTD_human
TgeneNBASC0038356Stomach Neoplasms1CTD_human
TgeneNBASC3541319SHORT STATURE, OPTIC NERVE ATROPHY, AND PELGER-HUET ANOMALY1ORPHANET;UNIPROT
TgeneNBASC3809651INFANTILE LIVER FAILURE SYNDROME 21ORPHANET;UNIPROT