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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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Fusion gene ID: 24661

FusionGeneSummary for NPAS2_CNOT11

check button Fusion gene summary
Fusion gene informationFusion gene name: NPAS2_CNOT11
Fusion gene ID: 24661
HgeneTgene
Gene symbol

NPAS2

CNOT11

Gene ID

4862

55571

Gene nameneuronal PAS domain protein 2CCR4-NOT transcription complex subunit 11
SynonymsMOP4|PASD4|bHLHe9C2orf29|C40
Cytomap

2q11.2

2q11.2

Type of geneprotein-codingprotein-coding
Descriptionneuronal PAS domain-containing protein 2PAS domain-containing protein 4basic-helix-loop-helix-PAS protein MOP4class E basic helix-loop-helix protein 9member of PAS protein 4member of PAS superfamily 4neuronal PAS2CCR4-NOT transcription complex subunit 11UPF0760 protein C2orf29
Modification date2018051920180519
UniProtAcc

Q99743

Q9UKZ1

Ensembl transtripts involved in fusion geneENST00000335681, ENST00000542504, 
ENST00000486017, 
ENST00000289382, 
Fusion gene scores* DoF score6 X 5 X 5=1501 X 1 X 1=1
# samples 61
** MAII scorelog2(6/150*10)=-1.32192809488736
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(1/1*10)=3.32192809488736
Context

PubMed: NPAS2 [Title/Abstract] AND CNOT11 [Title/Abstract] AND fusion [Title/Abstract]

Functional or gene categories assigned by FusionGDB annotationTumor suppressor gene involved fusion gene, in-frame but not retained their domain.
* 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
HgeneNPAS2

GO:0045893

positive regulation of transcription, DNA-templated

11441146

HgeneNPAS2

GO:0051775

response to redox state

11441146


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
TCGALDBLCATCGA-DK-A3IK-01ANPAS2chr2

101565942

+CNOT11chr2

101879001

+
* 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
In-frameENST00000335681ENST00000289382NPAS2chr2

101565942

+CNOT11chr2

101879001

+
In-frameENST00000542504ENST00000289382NPAS2chr2

101565942

+CNOT11chr2

101879001

+
3UTR-3CDSENST00000486017ENST00000289382NPAS2chr2

101565942

+CNOT11chr2

101879001

+

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FusionProtFeatures for NPAS2_CNOT11


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
NPAS2

Q99743

CNOT11

Q9UKZ1

Transcriptional activator which forms a core componentof the circadian clock. The circadian clock, an internal time-keeping system, regulates various physiological processes throughthe generation of approximately 24 hour circadian rhythms in geneexpression, which are translated into rhythms in metabolism andbehavior. It is derived from the Latin roots 'circa' (about) and'diem' (day) and acts as an important regulator of a wide array ofphysiological functions including metabolism, sleep, bodytemperature, blood pressure, endocrine, immune, cardiovascular,and renal function. Consists of two major components: the centralclock, residing in the suprachiasmatic nucleus (SCN) of the brain,and the peripheral clocks that are present in nearly every tissueand organ system. Both the central and peripheral clocks can bereset by environmental cues, also known as Zeitgebers (German for'timegivers'). The predominant Zeitgeber for the central clock islight, which is sensed by retina and signals directly to the SCN.The central clock entrains the peripheral clocks through neuronaland hormonal signals, body temperature and feeding-related cues,aligning all clocks with the external light/dark cycle. Circadianrhythms allow an organism to achieve temporal homeostasis with itsenvironment at the molecular level by regulating gene expressionto create a peak of protein expression once every 24 hours tocontrol when a particular physiological process is most activewith respect to the solar day. Transcription and translation ofcore clock components (CLOCK, NPAS2, ARNTL/BMAL1, ARNTL2/BMAL2,PER1, PER2, PER3, CRY1 and CRY2) plays a critical role in rhythmgeneration, whereas delays imposed by post-translationalmodifications (PTMs) are important for determining the period(tau) of the rhythms (tau refers to the period of a rhythm and isthe length, in time, of one complete cycle). A diurnal rhythm issynchronized with the day/night cycle, while the ultradian andinfradian rhythms have a period shorter and longer than 24 hours,respectively. Disruptions in the circadian rhythms contribute tothe pathology of cardiovascular diseases, cancer, metabolicsyndromes and aging. A transcription/translation feedback loop(TTFL) forms the core of the molecular circadian clock mechanism.Transcription factors, CLOCK or NPAS2 and ARNTL/BMAL1 orARNTL2/BMAL2, form the positive limb of the feedback loop, act inthe form of a heterodimer and activate the transcription of coreclock genes and clock-controlled genes (involved in key metabolicprocesses), harboring E-box elements (5'-CACGTG-3') within theirpromoters. The core clock genes: PER1/2/3 and CRY1/2 which aretranscriptional repressors form the negative limb of the feedbackloop and interact with the CLOCK|NPAS2-ARNTL/BMAL1|ARNTL2/BMAL2heterodimer inhibiting its activity and thereby negativelyregulating their own expression. This heterodimer also activatesnuclear receptors NR1D1/2 and RORA/B/G, which form a secondfeedback loop and which activate and repress ARNTL/BMAL1transcription, respectively. The NPAS2-ARNTL/BMAL1 heterodimerpositively regulates the expression of MAOA, F7 and LDHA andmodulates the circadian rhythm of daytime contrast sensitivity byregulating the rhythmic expression of adenylate cyclase type 1(ADCY1) in the retina. NPAS2 plays an important role in sleephomeostasis and in maintaining circadian behaviors in normallight/dark and feeding conditions and in the effectivesynchronization of feeding behavior with scheduled foodavailability. Regulates the gene transcription of key metabolicpathways in the liver and is involved in DNA damage response byregulating several cell cycle and DNA repair genes.{ECO:0000269|PubMed:11441146, ECO:0000269|PubMed:11441147,ECO:0000269|PubMed:14645221, ECO:0000269|PubMed:18439826,ECO:0000269|PubMed:18819933}. Component of the CCR4-NOT complex which is one of themajor cellular mRNA deadenylases and is linked to various cellularprocesses including bulk mRNA degradation, miRNA-mediatedrepression, translational repression during translationalinitiation and general transcription regulation. Additionalcomplex functions may be a consequence of its influence on mRNAexpression. Is required for the association of CNOT10 with theCCR4-NOT complex. Seems not to be required for complex deadenylasefunction.

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
HgeneNPAS2chr2:101565942chr2:101879001ENST00000335681+72182_152199825DomainPAS 1
HgeneNPAS2chr2:101565942chr2:101879001ENST00000335681+7219_59199825DomainbHLH
HgeneNPAS2chr2:101565942chr2:101879001ENST00000335681+7211_61199825RegionSufficient for heterodimer formation with ARNTL/BMAL1%2C E-box binding and for the effect of NADPH
TgeneCNOT11chr2:101565942chr2:101879001ENST00000289382+17287_290226511Compositional biasNote=Poly-Pro

- In-frame and not-retained protein feature among the 13 regional features.
>>
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneNPAS2chr2:101565942chr2:101879001ENST00000335681+721237_307199825DomainPAS 2
HgeneNPAS2chr2:101565942chr2:101879001ENST00000335681+721311_354199825DomainNote=PAC
TgeneCNOT11chr2:101565942chr2:101879001ENST00000289382+17155_180226511Compositional biasNote=Pro-rich
TgeneCNOT11chr2:101565942chr2:101879001ENST00000289382+173_59226511Compositional biasNote=Gly-rich


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FusionGeneSequence for NPAS2_CNOT11


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.
>In-frame_NPAS2_ENST00000335681_chr2_101565942_+_CNOT11_ENST00000289382_chr2_101879001_+_484aa
MDEDEKDRAKRASRNKSEKKRRDQFNVLIKELSSMLPGNTRKMDKTTVLEKVIGFLQKHNEVSAQTEICDIQQDWKPSFLSNEEFTQLML
EALDGFIIAVTTDGSIIYVSDSITPLLGHLPSDVMDQNLLNFLPEQEHSEVYKILSSHMLVTDSPSPEYLKSDSDLEFYCHLLRGSLNPK
EFPTYEYIKFVGNFRSYNNERQSELPTQSKASFPSILSDPDPDSSNSGFDSSVASQITEALVSGPKPPIESHFRPEFIRPPPPLHICEDE
LAWLNPTEPDHAIQWDKSMCVKNSTGVEIKRIMAKAFKSPLSSPQQTQLLGELEKDPKLVYHIGLTPAKLPDLVENNPLVAIEMLLKLMQ
SSQITEYFSVLVNMDMSLHSMEVVNRLTTAVDLPPEFIHLYISNCISTCEQIKDKYMQNRLVRLVCVFLQSLIRNKIINVQDLFIEVQAF

>In-frame_NPAS2_ENST00000542504_chr2_101565942_+_CNOT11_ENST00000289382_chr2_101879001_+_549aa
MYAYGFVGRCAPFPAEEGRTFDLSEELGRSVTREGTGTTRLNSEPVPLLCLPLLNCSRKNCIENLMDEDEKDRAKRASRNKSEKKRRDQF
NVLIKELSSMLPGNTRKMDKTTVLEKVIGFLQKHNEVSAQTEICDIQQDWKPSFLSNEEFTQLMLEALDGFIIAVTTDGSIIYVSDSITP
LLGHLPSDVMDQNLLNFLPEQEHSEVYKILSSHMLVTDSPSPEYLKSDSDLEFYCHLLRGSLNPKEFPTYEYIKFVGNFRSYNNERQSEL
PTQSKASFPSILSDPDPDSSNSGFDSSVASQITEALVSGPKPPIESHFRPEFIRPPPPLHICEDELAWLNPTEPDHAIQWDKSMCVKNST
GVEIKRIMAKAFKSPLSSPQQTQLLGELEKDPKLVYHIGLTPAKLPDLVENNPLVAIEMLLKLMQSSQITEYFSVLVNMDMSLHSMEVVN
RLTTAVDLPPEFIHLYISNCISTCEQIKDKYMQNRLVRLVCVFLQSLIRNKIINVQDLFIEVQAFCIEFSRIREAAGLFRLLKTLDTGET


* Fusion transcript sequences (only coding sequence (CDS) region).
>In-frame_NPAS2_ENST00000335681_chr2_101565942_+_CNOT11_ENST00000289382_chr2_101879001_+_1452nt
ATGGATGAAGATGAGAAAGACAGAGCCAAGAGAGCTTCTCGAAACAAGTCTGAGAAGAAGCGTCGGGACCAGTTCAATGTTCTCATCAAA
GAGCTCAGTTCCATGCTCCCTGGCAACACGCGGAAAATGGACAAAACCACCGTGTTGGAAAAGGTCATCGGATTTTTGCAGAAACACAAT
GAAGTCTCAGCGCAAACGGAAATCTGTGACATTCAGCAAGACTGGAAGCCTTCATTCCTCAGTAATGAAGAATTCACCCAGCTGATGTTG
GAGGCATTAGATGGCTTCATTATCGCAGTGACAACAGACGGCAGCATCATCTATGTCTCTGACAGTATCACGCCTCTCCTTGGGCATTTA
CCGTCGGATGTCATGGATCAGAATTTGTTAAATTTCCTCCCAGAACAAGAACATTCAGAAGTTTATAAAATCCTTTCTTCCCATATGCTT
GTGACGGATTCCCCCTCCCCAGAATACTTAAAATCTGACAGCGATTTAGAGTTTTATTGCCATCTTCTCAGAGGCAGCTTGAACCCAAAG
GAATTTCCAACTTATGAATACATAAAATTTGTAGGAAATTTTCGCTCTTACAACAATGAACGCCAATCTGAATTGCCAACGCAAAGCAAA
GCGAGCTTCCCCAGTATTCTCAGTGACCCAGACCCGGATTCTTCTAATTCTGGATTTGACAGCTCAGTTGCCTCTCAGATCACAGAAGCT
TTAGTCAGCGGACCAAAGCCACCTATTGAAAGCCATTTTCGACCAGAGTTTATTCGTCCACCGCCTCCACTCCACATTTGTGAGGATGAA
CTTGCTTGGCTAAACCCCACGGAGCCTGACCACGCGATCCAGTGGGATAAATCGATGTGTGTTAAGAATAGCACTGGTGTGGAGATCAAA
CGAATAATGGCCAAAGCCTTCAAAAGCCCCTTATCCTCTCCCCAACAAACACAGCTACTTGGTGAGTTGGAAAAAGACCCCAAACTTGTC
TACCATATTGGCCTCACCCCAGCCAAACTTCCTGACCTTGTGGAAAACAACCCTTTAGTCGCTATAGAAATGTTGCTGAAATTAATGCAG
TCAAGCCAGATCACTGAGTATTTCTCTGTCCTGGTCAATATGGACATGTCTTTACATTCAATGGAAGTTGTAAATCGACTAACTACAGCT
GTTGATCTACCTCCTGAATTTATTCACCTTTATATATCAAATTGCATCTCTACTTGTGAACAGATTAAGGATAAATATATGCAGAATCGG
TTGGTGCGTCTTGTGTGTGTGTTTCTCCAATCCTTGATCCGTAACAAAATTATTAATGTACAGGATTTGTTTATAGAAGTGCAGGCATTC
TGTATTGAATTCAGTAGGATACGAGAAGCTGCTGGTCTTTTCCGGTTGTTGAAGACATTGGATACTGGGGAAACACCTTCTGAGACCAAA

>In-frame_NPAS2_ENST00000542504_chr2_101565942_+_CNOT11_ENST00000289382_chr2_101879001_+_1647nt
ATGTATGCGTATGGTTTTGTTGGGAGATGTGCCCCTTTCCCAGCCGAGGAGGGACGCACCTTTGACCTTTCTGAAGAGCTGGGCAGGTCG
GTAACCAGGGAAGGGACAGGCACCACCCGGCTAAATTCAGAACCAGTCCCGCTCCTCTGCTTGCCACTCCTTAATTGCTCAAGGAAAAAC
TGCATAGAAAATCTAATGGATGAAGATGAGAAAGACAGAGCCAAGAGAGCTTCTCGAAACAAGTCTGAGAAGAAGCGTCGGGACCAGTTC
AATGTTCTCATCAAAGAGCTCAGTTCCATGCTCCCTGGCAACACGCGGAAAATGGACAAAACCACCGTGTTGGAAAAGGTCATCGGATTT
TTGCAGAAACACAATGAAGTCTCAGCGCAAACGGAAATCTGTGACATTCAGCAAGACTGGAAGCCTTCATTCCTCAGTAATGAAGAATTC
ACCCAGCTGATGTTGGAGGCATTAGATGGCTTCATTATCGCAGTGACAACAGACGGCAGCATCATCTATGTCTCTGACAGTATCACGCCT
CTCCTTGGGCATTTACCGTCGGATGTCATGGATCAGAATTTGTTAAATTTCCTCCCAGAACAAGAACATTCAGAAGTTTATAAAATCCTT
TCTTCCCATATGCTTGTGACGGATTCCCCCTCCCCAGAATACTTAAAATCTGACAGCGATTTAGAGTTTTATTGCCATCTTCTCAGAGGC
AGCTTGAACCCAAAGGAATTTCCAACTTATGAATACATAAAATTTGTAGGAAATTTTCGCTCTTACAACAATGAACGCCAATCTGAATTG
CCAACGCAAAGCAAAGCGAGCTTCCCCAGTATTCTCAGTGACCCAGACCCGGATTCTTCTAATTCTGGATTTGACAGCTCAGTTGCCTCT
CAGATCACAGAAGCTTTAGTCAGCGGACCAAAGCCACCTATTGAAAGCCATTTTCGACCAGAGTTTATTCGTCCACCGCCTCCACTCCAC
ATTTGTGAGGATGAACTTGCTTGGCTAAACCCCACGGAGCCTGACCACGCGATCCAGTGGGATAAATCGATGTGTGTTAAGAATAGCACT
GGTGTGGAGATCAAACGAATAATGGCCAAAGCCTTCAAAAGCCCCTTATCCTCTCCCCAACAAACACAGCTACTTGGTGAGTTGGAAAAA
GACCCCAAACTTGTCTACCATATTGGCCTCACCCCAGCCAAACTTCCTGACCTTGTGGAAAACAACCCTTTAGTCGCTATAGAAATGTTG
CTGAAATTAATGCAGTCAAGCCAGATCACTGAGTATTTCTCTGTCCTGGTCAATATGGACATGTCTTTACATTCAATGGAAGTTGTAAAT
CGACTAACTACAGCTGTTGATCTACCTCCTGAATTTATTCACCTTTATATATCAAATTGCATCTCTACTTGTGAACAGATTAAGGATAAA
TATATGCAGAATCGGTTGGTGCGTCTTGTGTGTGTGTTTCTCCAATCCTTGATCCGTAACAAAATTATTAATGTACAGGATTTGTTTATA
GAAGTGCAGGCATTCTGTATTGAATTCAGTAGGATACGAGAAGCTGCTGGTCTTTTCCGGTTGTTGAAGACATTGGATACTGGGGAAACA


* Fusion transcript sequences (Full-length transcript).
>In-frame_NPAS2_ENST00000335681_chr2_101565942_+_CNOT11_ENST00000289382_chr2_101879001_+_2640nt
TTTGCCGCGCGAGCAGCCGGCCTCTCGCAGGAGCCGAGGGACCCGCGCGGCTGCGGCCCAGGAGCGGCGGCCGCGGAGCCCGGAGACCCG
CAGCCGCGGCGGCGGCGGCGGCGGCGGCAGCAGCTAGAGCAGCGCCTCCCGCCGCCGCCCGGGAGGAGCTCGCCGCGCCCGCTCGCCGCC
TCGTCTCCCAGCGGCGGCGGGAGGCGCGTCTCCCCGGCCCAGTCCGCGCCCGGCCCCGCGGGGCCGCTCCGGCCCGCTCCGAGGAAAAAC
TGCATAGAAAATCTAATGGATGAAGATGAGAAAGACAGAGCCAAGAGAGCTTCTCGAAACAAGTCTGAGAAGAAGCGTCGGGACCAGTTC
AATGTTCTCATCAAAGAGCTCAGTTCCATGCTCCCTGGCAACACGCGGAAAATGGACAAAACCACCGTGTTGGAAAAGGTCATCGGATTT
TTGCAGAAACACAATGAAGTCTCAGCGCAAACGGAAATCTGTGACATTCAGCAAGACTGGAAGCCTTCATTCCTCAGTAATGAAGAATTC
ACCCAGCTGATGTTGGAGGCATTAGATGGCTTCATTATCGCAGTGACAACAGACGGCAGCATCATCTATGTCTCTGACAGTATCACGCCT
CTCCTTGGGCATTTACCGTCGGATGTCATGGATCAGAATTTGTTAAATTTCCTCCCAGAACAAGAACATTCAGAAGTTTATAAAATCCTT
TCTTCCCATATGCTTGTGACGGATTCCCCCTCCCCAGAATACTTAAAATCTGACAGCGATTTAGAGTTTTATTGCCATCTTCTCAGAGGC
AGCTTGAACCCAAAGGAATTTCCAACTTATGAATACATAAAATTTGTAGGAAATTTTCGCTCTTACAACAATGAACGCCAATCTGAATTG
CCAACGCAAAGCAAAGCGAGCTTCCCCAGTATTCTCAGTGACCCAGACCCGGATTCTTCTAATTCTGGATTTGACAGCTCAGTTGCCTCT
CAGATCACAGAAGCTTTAGTCAGCGGACCAAAGCCACCTATTGAAAGCCATTTTCGACCAGAGTTTATTCGTCCACCGCCTCCACTCCAC
ATTTGTGAGGATGAACTTGCTTGGCTAAACCCCACGGAGCCTGACCACGCGATCCAGTGGGATAAATCGATGTGTGTTAAGAATAGCACT
GGTGTGGAGATCAAACGAATAATGGCCAAAGCCTTCAAAAGCCCCTTATCCTCTCCCCAACAAACACAGCTACTTGGTGAGTTGGAAAAA
GACCCCAAACTTGTCTACCATATTGGCCTCACCCCAGCCAAACTTCCTGACCTTGTGGAAAACAACCCTTTAGTCGCTATAGAAATGTTG
CTGAAATTAATGCAGTCAAGCCAGATCACTGAGTATTTCTCTGTCCTGGTCAATATGGACATGTCTTTACATTCAATGGAAGTTGTAAAT
CGACTAACTACAGCTGTTGATCTACCTCCTGAATTTATTCACCTTTATATATCAAATTGCATCTCTACTTGTGAACAGATTAAGGATAAA
TATATGCAGAATCGGTTGGTGCGTCTTGTGTGTGTGTTTCTCCAATCCTTGATCCGTAACAAAATTATTAATGTACAGGATTTGTTTATA
GAAGTGCAGGCATTCTGTATTGAATTCAGTAGGATACGAGAAGCTGCTGGTCTTTTCCGGTTGTTGAAGACATTGGATACTGGGGAAACA
CCTTCTGAGACCAAAATGTCAAAATAATACCTCATCAGAACCATCCCATCCATTCACTGTTCAGCTGTACTGTGATTTAGTTTTTACACC
GTTAAAACCCTGAGTGGATTGCTTGGTTTAATGCATATAAACAGTACTTTATCTACTTAAAGCAAAGTTTTGCTTTCTTGAATGACTTTT
TCTGTGAGATGAATTTTTGATAAGAACTAGGGAAAACATGTCTTTTAGGTGTCTTGCTGATGACTATCCATAGGAGGAATGGCTATCCCA
AAAAAAGTTCCGCAAAAAAGTAGATGAGTTTCTTTTTTTTTTAAGCACTAAAGAACAAAATGCATTTTTCATTAATACAGGCTTCTGATG
AACCAGGAATCCTGTTTTCGTAAAGTTCCAATGTTGATGAGAGTAAATTCTTAAGCATTTGTCCTAGAGGTGAAAGCAGCTGAATGTTTC
TGAACCATCAAGAGGCAAACAAACAGGAGTTTGTTTCTTGAACCTGCTTATGCACACAGCTCTTAACTCCTCATGAGGCACACAGCTCTT
AACTCCTGATGAACCAAGGATTTACTCATAACTTTCTCCTTGTCATGGAGGCTTAATAGACAACAGAATAAATGCATTTCTTGGGCCTCT
TATAAACTTGGGAATTCTTAGAAAGCTGCTTCTATTACCAGGCTGTAATAGCTGGTATAGTTTTTTTTTTTTCTCTTAAGATGTTCTGTT
ATTAGTCTGAGACAGCCATTTTTTTGTTTTAAGGAAAAATATCAGTCAGTGCTCCGGGAGGTAATTTCCTGTGGGGTCTGCACCCTCCTG
TCTGGGTGGTGGATGTGGGTTTGAGAAGTAGGAGAGCAGGGTGGTACCGTGTGGGCTCTTACCCTTTATGTGATTTTGGACAACAGTGCC

>In-frame_NPAS2_ENST00000542504_chr2_101565942_+_CNOT11_ENST00000289382_chr2_101879001_+_2552nt
GGATGTATGCGTATGGTTTTGTTGGGAGATGTGCCCCTTTCCCAGCCGAGGAGGGACGCACCTTTGACCTTTCTGAAGAGCTGGGCAGGT
CGGTAACCAGGGAAGGGACAGGCACCACCCGGCTAAATTCAGAACCAGTCCCGCTCCTCTGCTTGCCACTCCTTAATTGCTCAAGGAAAA
ACTGCATAGAAAATCTAATGGATGAAGATGAGAAAGACAGAGCCAAGAGAGCTTCTCGAAACAAGTCTGAGAAGAAGCGTCGGGACCAGT
TCAATGTTCTCATCAAAGAGCTCAGTTCCATGCTCCCTGGCAACACGCGGAAAATGGACAAAACCACCGTGTTGGAAAAGGTCATCGGAT
TTTTGCAGAAACACAATGAAGTCTCAGCGCAAACGGAAATCTGTGACATTCAGCAAGACTGGAAGCCTTCATTCCTCAGTAATGAAGAAT
TCACCCAGCTGATGTTGGAGGCATTAGATGGCTTCATTATCGCAGTGACAACAGACGGCAGCATCATCTATGTCTCTGACAGTATCACGC
CTCTCCTTGGGCATTTACCGTCGGATGTCATGGATCAGAATTTGTTAAATTTCCTCCCAGAACAAGAACATTCAGAAGTTTATAAAATCC
TTTCTTCCCATATGCTTGTGACGGATTCCCCCTCCCCAGAATACTTAAAATCTGACAGCGATTTAGAGTTTTATTGCCATCTTCTCAGAG
GCAGCTTGAACCCAAAGGAATTTCCAACTTATGAATACATAAAATTTGTAGGAAATTTTCGCTCTTACAACAATGAACGCCAATCTGAAT
TGCCAACGCAAAGCAAAGCGAGCTTCCCCAGTATTCTCAGTGACCCAGACCCGGATTCTTCTAATTCTGGATTTGACAGCTCAGTTGCCT
CTCAGATCACAGAAGCTTTAGTCAGCGGACCAAAGCCACCTATTGAAAGCCATTTTCGACCAGAGTTTATTCGTCCACCGCCTCCACTCC
ACATTTGTGAGGATGAACTTGCTTGGCTAAACCCCACGGAGCCTGACCACGCGATCCAGTGGGATAAATCGATGTGTGTTAAGAATAGCA
CTGGTGTGGAGATCAAACGAATAATGGCCAAAGCCTTCAAAAGCCCCTTATCCTCTCCCCAACAAACACAGCTACTTGGTGAGTTGGAAA
AAGACCCCAAACTTGTCTACCATATTGGCCTCACCCCAGCCAAACTTCCTGACCTTGTGGAAAACAACCCTTTAGTCGCTATAGAAATGT
TGCTGAAATTAATGCAGTCAAGCCAGATCACTGAGTATTTCTCTGTCCTGGTCAATATGGACATGTCTTTACATTCAATGGAAGTTGTAA
ATCGACTAACTACAGCTGTTGATCTACCTCCTGAATTTATTCACCTTTATATATCAAATTGCATCTCTACTTGTGAACAGATTAAGGATA
AATATATGCAGAATCGGTTGGTGCGTCTTGTGTGTGTGTTTCTCCAATCCTTGATCCGTAACAAAATTATTAATGTACAGGATTTGTTTA
TAGAAGTGCAGGCATTCTGTATTGAATTCAGTAGGATACGAGAAGCTGCTGGTCTTTTCCGGTTGTTGAAGACATTGGATACTGGGGAAA
CACCTTCTGAGACCAAAATGTCAAAATAATACCTCATCAGAACCATCCCATCCATTCACTGTTCAGCTGTACTGTGATTTAGTTTTTACA
CCGTTAAAACCCTGAGTGGATTGCTTGGTTTAATGCATATAAACAGTACTTTATCTACTTAAAGCAAAGTTTTGCTTTCTTGAATGACTT
TTTCTGTGAGATGAATTTTTGATAAGAACTAGGGAAAACATGTCTTTTAGGTGTCTTGCTGATGACTATCCATAGGAGGAATGGCTATCC
CAAAAAAAGTTCCGCAAAAAAGTAGATGAGTTTCTTTTTTTTTTAAGCACTAAAGAACAAAATGCATTTTTCATTAATACAGGCTTCTGA
TGAACCAGGAATCCTGTTTTCGTAAAGTTCCAATGTTGATGAGAGTAAATTCTTAAGCATTTGTCCTAGAGGTGAAAGCAGCTGAATGTT
TCTGAACCATCAAGAGGCAAACAAACAGGAGTTTGTTTCTTGAACCTGCTTATGCACACAGCTCTTAACTCCTCATGAGGCACACAGCTC
TTAACTCCTGATGAACCAAGGATTTACTCATAACTTTCTCCTTGTCATGGAGGCTTAATAGACAACAGAATAAATGCATTTCTTGGGCCT
CTTATAAACTTGGGAATTCTTAGAAAGCTGCTTCTATTACCAGGCTGTAATAGCTGGTATAGTTTTTTTTTTTTCTCTTAAGATGTTCTG
TTATTAGTCTGAGACAGCCATTTTTTTGTTTTAAGGAAAAATATCAGTCAGTGCTCCGGGAGGTAATTTCCTGTGGGGTCTGCACCCTCC
TGTCTGGGTGGTGGATGTGGGTTTGAGAAGTAGGAGAGCAGGGTGGTACCGTGTGGGCTCTTACCCTTTATGTGATTTTGGACAACAGTG


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FusionGenePPI for NPAS2_CNOT11


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
NPAS2EP300, NCOA3, KAT2B, CREBBP, RXRA, RARA, ARNTL, HSP90AA1, HESX1, RHOXF1, ZSCAN1, TRAF4, RPL6, ARNT2, ARNTL2, CRX, EFS, HGS, RASSF7, SHMT2, CLOCK, CRY1, CSNK2B, DEC1, RORC, CRY2CNOT11ELAVL1, NLK, CT55, MMP7, CAPZA2, CNOT7, BTRC, MED4, OFD1, CEP120, CNTROB, XPO1, CNOT2, CNOT1, RC3H1, CNOT6, CNOT6L, CNOT10, NANOS2, TNKS1BP1, CNOT3, RIBC1, CNOT8, RAVER1, TOB1, GPBP1L1, BTG3, RQCD1, TEX13A, GADD45B, GGNBP2, FHL2, TBC1D10A, EDRF1, IZUMO1, FBXW11, MAP4K4, GLA, NFKB1


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 NPAS2_CNOT11


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 NPAS2_CNOT11


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNPAS2C0005586Bipolar Disorder5PSYGENET
HgeneNPAS2C0085159Seasonal Affective Disorder4PSYGENET
HgeneNPAS2C0011581Depressive disorder2PSYGENET
HgeneNPAS2C0004352Autistic Disorder1CTD_human
HgeneNPAS2C0011570Mental Depression1PSYGENET
HgeneNPAS2C0023893Liver Cirrhosis, Experimental1CTD_human
HgeneNPAS2C0036337Schizoaffective Disorder1PSYGENET
HgeneNPAS2C0036341Schizophrenia1PSYGENET