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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: 12582

FusionGeneSummary for FAM149B1_ADK

check button Fusion gene summary
Fusion gene informationFusion gene name: FAM149B1_ADK
Fusion gene ID: 12582
HgeneTgene
Gene symbol

FAM149B1

ADK

Gene ID

317662

132

Gene namefamily with sequence similarity 149 member B1adenosine kinase
SynonymsKIAA0974AK
Cytomap

10q22.2

10q22.2|10q11-q24

Type of geneprotein-codingprotein-coding
Descriptionprotein FAM149B1adenosine kinaseadenosine 5'-phosphotransferasetesticular tissue protein Li 14
Modification date2018051920180523
UniProtAcc

Q96BN6

P55263

Ensembl transtripts involved in fusion geneENST00000242505, ENST00000607940, 
ENST00000539909, ENST00000286621, 
ENST00000372734, ENST00000541550, 
ENST00000467840, 
Fusion gene scores* DoF score3 X 2 X 2=1218 X 8 X 11=1584
# samples 321
** MAII scorelog2(3/12*10)=1.32192809488736
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(21/1584*10)=-2.91511110241349
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: FAM149B1 [Title/Abstract] AND ADK [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
TCGARVGBMTCGA-28-5204-01AFAM149B1chr10

74970196

+ADKchr10

76349040

+
* 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
Frame-shiftENST00000242505ENST00000539909FAM149B1chr10

74970196

+ADKchr10

76349040

+
Frame-shiftENST00000242505ENST00000286621FAM149B1chr10

74970196

+ADKchr10

76349040

+
Frame-shiftENST00000242505ENST00000372734FAM149B1chr10

74970196

+ADKchr10

76349040

+
Frame-shiftENST00000242505ENST00000541550FAM149B1chr10

74970196

+ADKchr10

76349040

+
5CDS-intronENST00000242505ENST00000467840FAM149B1chr10

74970196

+ADKchr10

76349040

+
intron-3CDSENST00000607940ENST00000539909FAM149B1chr10

74970196

+ADKchr10

76349040

+
intron-3CDSENST00000607940ENST00000286621FAM149B1chr10

74970196

+ADKchr10

76349040

+
intron-3CDSENST00000607940ENST00000372734FAM149B1chr10

74970196

+ADKchr10

76349040

+
intron-3CDSENST00000607940ENST00000541550FAM149B1chr10

74970196

+ADKchr10

76349040

+
intron-intronENST00000607940ENST00000467840FAM149B1chr10

74970196

+ADKchr10

76349040

+

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FusionProtFeatures for FAM149B1_ADK


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
FAM149B1

Q96BN6

ADK

P55263


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 FAM149B1_ADK


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 FAM149B1_ADK


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
FAM149B1TBC1D32, CFAP20ADKFICD, SRD5A3, ASS1, CAPG, DAZAP1, KYNU, LDHA, PIR, PTGR1, SOD1, NNMT, NQO1, PCBP1, PITPNB, RBM12, NPLOC4, FGB


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 FAM149B1_ADK


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneADKP55263DB00811RibavirinAdenosine kinasesmall moleculeapproved

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RelatedDiseases for FAM149B1_ADK


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneADKC0036341Schizophrenia1PSYGENET
TgeneADKC0242184Hypoxia1CTD_human
TgeneADKC3280381HYPERMETHIONINEMIA DUE TO ADENOSINE KINASE DEFICIENCY1CTD_human;ORPHANET;UNIPROT
TgeneADKC3714756Intellectual Disability1CTD_human