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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: 22265

FusionGeneSummary for MOB3B_C9orf72

check button Fusion gene summary
Fusion gene informationFusion gene name: MOB3B_C9orf72
Fusion gene ID: 22265
HgeneTgene
Gene symbol

MOB3B

C9orf72

Gene ID

79817

203228

Gene nameMOB kinase activator 3Bchromosome 9 open reading frame 72
SynonymsC9orf35|MOB1D|MOBKL2BALSFTD|DENNL72|FTDALS|FTDALS1
Cytomap

9p21.2

9p21.2

Type of geneprotein-codingprotein-coding
DescriptionMOB kinase activator 3BMOB kinase activator-like 2BMOB1, Mps One Binder kinase activator-like 2Bmob1 homolog 2bmonopolar spindle 1 binding, MOB1, domain containingmps one binder kinase activator-like 2Bguanine nucleotide exchange C9orf72protein C9orf72
Modification date2018051920180527
UniProtAcc

Q86TA1

Q96LT7

Ensembl transtripts involved in fusion geneENST00000262244, ENST00000603061, 
ENST00000380003, ENST00000488117, 
ENST00000379997, 
Fusion gene scores* DoF score4 X 2 X 4=322 X 2 X 2=8
# samples 42
** MAII scorelog2(4/32*10)=0.321928094887362
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(2/8*10)=1.32192809488736
Context

PubMed: MOB3B [Title/Abstract] AND C9orf72 [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
TCGALDCOADTCGA-A6-2674-01AMOB3Bchr9

27529553

-C9orf72chr9

27567162

-
* 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
5UTR-5UTRENST00000262244ENST00000380003MOB3Bchr9

27529553

-C9orf72chr9

27567162

-
5UTR-5UTRENST00000262244ENST00000488117MOB3Bchr9

27529553

-C9orf72chr9

27567162

-
5UTR-5UTRENST00000262244ENST00000379997MOB3Bchr9

27529553

-C9orf72chr9

27567162

-
intron-5UTRENST00000603061ENST00000380003MOB3Bchr9

27529553

-C9orf72chr9

27567162

-
intron-5UTRENST00000603061ENST00000488117MOB3Bchr9

27529553

-C9orf72chr9

27567162

-
intron-5UTRENST00000603061ENST00000379997MOB3Bchr9

27529553

-C9orf72chr9

27567162

-

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FusionProtFeatures for MOB3B_C9orf72


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MOB3B

Q86TA1

C9orf72

Q96LT7

May regulate the activity of kinases. {ECO:0000250}. Component of the C9orf72-SMCR8 complex, a complex thathas guanine nucleotide exchange factor (GEF) activity andregulates autophagy (PubMed:27193190, PubMed:27103069,PubMed:27617292, PubMed:28195531). In the complex, C9orf72 andSMCR8 probably constitute the catalytic subunits that promote theexchange of GDP to GTP, converting inactive GDP-bound RAB8A andRAB39B into their active GTP-bound form, thereby promotingautophagosome maturation (PubMed:27103069). The C9orf72-SMCR8complex also acts as a regulator of autophagy initiation byinteracting with the ATG1/ULK1 kinase complex and modulating itsprotein kinase activity (PubMed:27617292). Positively regulatesinitiation of autophagy by regulating the RAB1A-dependenttrafficking of the ATG1/ULK1 kinase complex to the phagophorewhich leads to autophagosome formation (PubMed:27334615). Acts asa regulator of mTORC1 signaling by promoting phosphorylation ofmTORC1 substrates (PubMed:27559131). Plays a role in endosomaltrafficking (PubMed:24549040). May be involved in regulating thematuration of phagosomes to lysosomes (By similarity). Regulatesactin dynamics in motor neurons by inhibiting the GTP-bindingactivity of ARF6, leading to ARF6 inactivation (PubMed:27723745).This reduces the activity of the LIMK1 and LIMK2 kinases which areresponsible for phosphorylation and inactivation of cofilin,leading to cofilin activation (PubMed:27723745). Positivelyregulates axon extension and axon growth cone size in spinal motorneurons (PubMed:27723745). Plays a role within the hematopoieticsystem in restricting inflammation and the development ofautoimmunity (By similarity). {ECO:0000250|UniProtKB:Q6DFW0,ECO:0000269|PubMed:24549040, ECO:0000269|PubMed:27103069,ECO:0000269|PubMed:27193190, ECO:0000269|PubMed:27334615,ECO:0000269|PubMed:27559131, ECO:0000269|PubMed:27617292,ECO:0000269|PubMed:27723745, ECO:0000269|PubMed:28195531}. Isoform 1: Regulates stress granule assembly in responseto cellular stress. {ECO:0000269|PubMed:27037575}. Isoform 2: Does not play a role in regulation of stressgranule assembly in response to cellular stress.{ECO:0000269|PubMed:27037575}.

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 MOB3B_C9orf72


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 MOB3B_C9orf72


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
MOB3BNT5C2, CNKSR2, MAPK14, PPBP, ELAVL1, LATS1, LATS2C9orf72ELAVL1, APP, MMS19, SRPK1, CRX, REL, EIF2B2, NMI


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 MOB3B_C9orf72


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 MOB3B_C9orf72


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgeneC9orf72C0033975Psychotic Disorders3PSYGENET
TgeneC9orf72C0349204Nonorganic psychosis3PSYGENET
TgeneC9orf72C0036341Schizophrenia2PSYGENET
TgeneC9orf72C0005586Bipolar Disorder1PSYGENET
TgeneC9orf72C0036337Schizoaffective Disorder1PSYGENET
TgeneC9orf72C3495559Juvenile arthritis1CTD_human
TgeneC9orf72C3888102Frontotemporal Dementia With Motor Neuron Disease1CTD_human