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Center for Computational Systems Medicine level1
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Fusion Gene Summary

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Fusion Gene Sample Information

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Fusion ORF Analysis

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Fusion Amino Acid Sequences

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Fusion Protein Functional Features

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Fusion Protein-Protein Interaction

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Related drugs with this fusion protein

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Related disease with this fusion protein

Fusion Protein:NIN-NEMF

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NIN-NEMF
FusionPDB ID: 59159
FusionGDB2.0 ID: 59159
HgeneTgene
Gene symbol

NIN

NEMF

Gene ID

51199

9147

Gene namenineinnuclear export mediator factor
SynonymsSCKL7NY-CO-1|SDCCAG1
Cytomap

14q22.1

14q21.3

Type of geneprotein-codingprotein-coding
Descriptionnineinglycogen synthase kinase 3 beta-interacting proteinhNineinninein (GSK3B interacting protein)ninein centrosomal proteinnuclear export mediator factor NEMFantigen NY-CO-1serologically defined colon cancer antigen 1
Modification date2020032820200313
UniProtAcc

Q9Y2I6

O60524

Ensembl transtripts involved in fusion geneENST idsENST00000245441, ENST00000324330, 
ENST00000382041, ENST00000382043, 
ENST00000389868, ENST00000453196, 
ENST00000530997, ENST00000486200, 
ENST00000546046, ENST00000556925, 
ENST00000382135, ENST00000545773, 
ENST00000556672, ENST00000298310, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score16 X 18 X 9=25926 X 8 X 4=192
# samples 209
** MAII scorelog2(20/2592*10)=-3.6959938131099
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(9/192*10)=-1.09310940439148
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: NIN [Title/Abstract] AND NEMF [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NIN(51273455)-NEMF(50292673), # samples:2
Anticipated loss of major functional domain due to fusion event.NIN-NEMF seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
NIN-NEMF seems lost the major protein functional domain in Hgene partner, which is a CGC by not retaining the major functional domain in the partially deleted in-frame ORF.
NIN-NEMF seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
NIN-NEMF seems lost the major protein functional domain in Hgene partner, which is a essential gene by not retaining the major functional domain in the partially deleted in-frame ORF.
NIN-NEMF seems lost the major protein functional domain in Hgene partner, which is a CGC due to the frame-shifted ORF.
NIN-NEMF seems lost the major protein functional domain in Hgene partner, which is a essential gene due to the frame-shifted ORF.
NIN-NEMF seems lost the major protein functional domain in Tgene partner, which is a essential gene due to the frame-shifted ORF.
* 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 buttonFusion gene breakpoints across NIN (5'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure

check buttonFusion gene breakpoints across NEMF (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


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Fusion Gene Sample Information

check buttonFusion gene information from FusionGDB2.0.
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-BH-A1FE-01ANINchr14

51273455

-NEMFchr14

50292673

-


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Fusion ORF Analysis


check buttonFusion information from ORFfinder translation from full-length transcript sequence from FusionPDB.
HenstTenstHgeneHchrHbpHstrandTgeneTchrTbpTstrandSeq length
(transcript)
BP loci
(transcript)
Predicted start
(transcript)
Predicted stop
(transcript)
Seq length
(amino acids)
ENST00000389868NINchr1451273455-ENST00000298310NEMFchr1450292673-35564564322198588
ENST00000382043NINchr1451273455-ENST00000298310NEMFchr1450292673-34023022782044588
ENST00000324330NINchr1451273455-ENST00000298310NEMFchr1450292673-35564564322198588

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
ENST00000389868ENST00000298310NINchr1451273455-NEMFchr1450292673-0.0003108780.9996891
ENST00000382043ENST00000298310NINchr1451273455-NEMFchr1450292673-0.0003458370.9996542
ENST00000324330ENST00000298310NINchr1451273455-NEMFchr1450292673-0.0003108780.9996891

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Fusion Amino Acid Sequences


check button For individual full-length fusion transcript sequence from FusionPDB, we ran ORFfinder and chose the longest ORF among the all predicted ones.
>FusionGDB ID_FusionGDB isoform ID_FGname_Hgene_Hchr_Hbp_Henst_Tgene_Tchr_Tbp_Tenst_length(fusion AA) seq_BP

>59159_59159_1_NIN-NEMF_NIN_chr14_51273455_ENST00000324330_NEMF_chr14_50292673_ENST00000298310_length(amino acids)=588AA_BP=8
MKNTFKNQAFKSAEKKTKQTLKEVQTVTSIQKARKVYWFEKFLWFISSENYLIIGGRDQQQNEIIVKRYLTPGDIYVHADLHGATSCVIK
NPTGEPIPPRTLTEAGTMALCYSAAWDARVITSAWWVYHHQVSKTAPTGEYLTTGSFMIRGKKNFLPPSYLMMGFSFLFKVDESCVWRHQ
GERKVRVQDEDMETLASCTSELISEEMEQLDGGDTSSDEDKEEHETPVEVELMTQVDQEDITLQSGRDELNEELIQEESSEDEGEYEEVR
KDQDSVGEMKDEGEETLNYPDTTIDLSHLQPQRSIQKLASKEESSNSSDSKSQSRRHLSAKERREMKKKKLPSDSGDLEALEGKDKEKES
TVHIETHQNTSKNVAAVQPMKRGQKSKMKKMKEKYKDQDEEDRELIMKLLGSAGSNKEEKGKKGKKGKTKDEPVKKQPQKPRGGQRVSDN
IKKETPFLEVITHELQDFAVDDPHDDKEEQDLDQQGNEENLFDSLTGQPHPEDVLLFAIPICAPYTTMTNYKYKVKLTPGVQKKGKAAKT

--------------------------------------------------------------

>59159_59159_2_NIN-NEMF_NIN_chr14_51273455_ENST00000382043_NEMF_chr14_50292673_ENST00000298310_length(amino acids)=588AA_BP=8
MKNTFKNQAFKSAEKKTKQTLKEVQTVTSIQKARKVYWFEKFLWFISSENYLIIGGRDQQQNEIIVKRYLTPGDIYVHADLHGATSCVIK
NPTGEPIPPRTLTEAGTMALCYSAAWDARVITSAWWVYHHQVSKTAPTGEYLTTGSFMIRGKKNFLPPSYLMMGFSFLFKVDESCVWRHQ
GERKVRVQDEDMETLASCTSELISEEMEQLDGGDTSSDEDKEEHETPVEVELMTQVDQEDITLQSGRDELNEELIQEESSEDEGEYEEVR
KDQDSVGEMKDEGEETLNYPDTTIDLSHLQPQRSIQKLASKEESSNSSDSKSQSRRHLSAKERREMKKKKLPSDSGDLEALEGKDKEKES
TVHIETHQNTSKNVAAVQPMKRGQKSKMKKMKEKYKDQDEEDRELIMKLLGSAGSNKEEKGKKGKKGKTKDEPVKKQPQKPRGGQRVSDN
IKKETPFLEVITHELQDFAVDDPHDDKEEQDLDQQGNEENLFDSLTGQPHPEDVLLFAIPICAPYTTMTNYKYKVKLTPGVQKKGKAAKT

--------------------------------------------------------------

>59159_59159_3_NIN-NEMF_NIN_chr14_51273455_ENST00000389868_NEMF_chr14_50292673_ENST00000298310_length(amino acids)=588AA_BP=8
MKNTFKNQAFKSAEKKTKQTLKEVQTVTSIQKARKVYWFEKFLWFISSENYLIIGGRDQQQNEIIVKRYLTPGDIYVHADLHGATSCVIK
NPTGEPIPPRTLTEAGTMALCYSAAWDARVITSAWWVYHHQVSKTAPTGEYLTTGSFMIRGKKNFLPPSYLMMGFSFLFKVDESCVWRHQ
GERKVRVQDEDMETLASCTSELISEEMEQLDGGDTSSDEDKEEHETPVEVELMTQVDQEDITLQSGRDELNEELIQEESSEDEGEYEEVR
KDQDSVGEMKDEGEETLNYPDTTIDLSHLQPQRSIQKLASKEESSNSSDSKSQSRRHLSAKERREMKKKKLPSDSGDLEALEGKDKEKES
TVHIETHQNTSKNVAAVQPMKRGQKSKMKKMKEKYKDQDEEDRELIMKLLGSAGSNKEEKGKKGKKGKTKDEPVKKQPQKPRGGQRVSDN
IKKETPFLEVITHELQDFAVDDPHDDKEEQDLDQQGNEENLFDSLTGQPHPEDVLLFAIPICAPYTTMTNYKYKVKLTPGVQKKGKAAKT

--------------------------------------------------------------

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Fusion Protein Functional Features


check button Four levels of functional features of fusion genes
Go to FGviewer search page for the most frequent breakpoint (https://ccsmweb.uth.edu/FGviewer/chr14:51273455/chr14:50292673)
- FGviewer provides the online visualization of the retention search of the protein functional features across DNA, RNA, protein, and pathological levels.
- How to search
1. Put your fusion gene symbol.
2. Press the tab key until there will be shown the breakpoint information filled.
4. Go down and press 'Search' tab twice.
4. Go down to have the hyperlink of the search result.
5. Click the hyperlink.
6. See the FGviewer result for your fusion gene.
FGviewer

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

Q9Y2I6

NEMF

O60524

FUNCTION: Involved in the microtubule organization in interphase cells. Overexpression induces the fragmentation of the Golgi, and causes lysosomes to disperse toward the cell periphery; it also interferes with mitotic spindle assembly. May play a role in ovarian carcinogenesis. {ECO:0000269|PubMed:12852856, ECO:0000269|PubMed:16254247, ECO:0000269|PubMed:18538832}.FUNCTION: Component of the ribosome quality control complex (RQC), a ribosome-associated complex that mediates ubiquitination and extraction of incompletely synthesized nascent chains for proteasomal degradation. NEMF is responsible for selective recognition of stalled 60S subunits by recognizing an exposed, nascent chain-conjugated tRNA moiety. NEMF is important for the stable association of LTN1 to the complex (PubMed:25578875). May indirectly play a role in nuclear export (PubMed:16103875). {ECO:0000269|PubMed:16103875, ECO:0000269|PubMed:25578875}.

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.
- Retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneNINchr14:51273455chr14:50292673ENST00000245441-43142_7788.333333333333332134.0DomainEF-hand 2
HgeneNINchr14:51273455chr14:50292673ENST00000245441-4318_4388.333333333333332134.0DomainEF-hand 1
HgeneNINchr14:51273455chr14:50292673ENST00000382041-43042_7788.333333333333332091.0DomainEF-hand 2
HgeneNINchr14:51273455chr14:50292673ENST00000382041-4308_4388.333333333333332091.0DomainEF-hand 1
HgeneNINchr14:51273455chr14:50292673ENST00000382043-32842_7788.333333333333331378.0DomainEF-hand 2
HgeneNINchr14:51273455chr14:50292673ENST00000382043-3288_4388.333333333333331378.0DomainEF-hand 1
HgeneNINchr14:51273455chr14:50292673ENST00000530997-22942_7788.333333333333332134.0DomainEF-hand 2
HgeneNINchr14:51273455chr14:50292673ENST00000530997-2298_4388.333333333333332134.0DomainEF-hand 1
TgeneNEMFchr14:51273455chr14:50292673ENST000002983101433869_894496.01077.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST0000038213509296_3590.0277.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST0000038213509483_5140.0277.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST0000038213509869_8940.0277.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST000005457731332483_514454.01035.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST000005457731332869_894454.01035.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST000005460461432869_894496.01056.0Coiled coilOntology_term=ECO:0000255

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneNINchr14:51273455chr14:50292673ENST00000245441-4311068_109988.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000245441-4311181_134188.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000245441-4311441_181688.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000245441-4311854_188588.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000245441-4311922_206788.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000245441-431357_57088.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000245441-431625_102788.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382041-4301068_109988.333333333333332091.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382041-4301181_134188.333333333333332091.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382041-4301441_181688.333333333333332091.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382041-4301854_188588.333333333333332091.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382041-4301922_206788.333333333333332091.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382041-430357_57088.333333333333332091.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382041-430625_102788.333333333333332091.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382043-3281068_109988.333333333333331378.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382043-3281181_134188.333333333333331378.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382043-3281441_181688.333333333333331378.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382043-3281854_188588.333333333333331378.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382043-3281922_206788.333333333333331378.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382043-328357_57088.333333333333331378.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000382043-328625_102788.333333333333331378.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000530997-2291068_109988.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000530997-2291181_134188.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000530997-2291441_181688.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000530997-2291854_188588.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000530997-2291922_206788.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000530997-229357_57088.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000530997-229625_102788.333333333333332134.0Coiled coilOntology_term=ECO:0000255
HgeneNINchr14:51273455chr14:50292673ENST00000245441-431182_21788.333333333333332134.0DomainEF-hand 3
HgeneNINchr14:51273455chr14:50292673ENST00000245441-431219_25288.333333333333332134.0DomainEF-hand 4
HgeneNINchr14:51273455chr14:50292673ENST00000245441-431317_35288.333333333333332134.0DomainEF-hand 5
HgeneNINchr14:51273455chr14:50292673ENST00000382041-430182_21788.333333333333332091.0DomainEF-hand 3
HgeneNINchr14:51273455chr14:50292673ENST00000382041-430219_25288.333333333333332091.0DomainEF-hand 4
HgeneNINchr14:51273455chr14:50292673ENST00000382041-430317_35288.333333333333332091.0DomainEF-hand 5
HgeneNINchr14:51273455chr14:50292673ENST00000382043-328182_21788.333333333333331378.0DomainEF-hand 3
HgeneNINchr14:51273455chr14:50292673ENST00000382043-328219_25288.333333333333331378.0DomainEF-hand 4
HgeneNINchr14:51273455chr14:50292673ENST00000382043-328317_35288.333333333333331378.0DomainEF-hand 5
HgeneNINchr14:51273455chr14:50292673ENST00000530997-229182_21788.333333333333332134.0DomainEF-hand 3
HgeneNINchr14:51273455chr14:50292673ENST00000530997-229219_25288.333333333333332134.0DomainEF-hand 4
HgeneNINchr14:51273455chr14:50292673ENST00000530997-229317_35288.333333333333332134.0DomainEF-hand 5
HgeneNINchr14:51273455chr14:50292673ENST00000245441-431245_25288.333333333333332134.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000245441-431300_30488.333333333333332134.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000245441-431420_42388.333333333333332134.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000382041-430245_25288.333333333333332091.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000382041-430300_30488.333333333333332091.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000382041-430420_42388.333333333333332091.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000382043-328245_25288.333333333333331378.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000382043-328300_30488.333333333333331378.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000382043-328420_42388.333333333333331378.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000530997-229245_25288.333333333333332134.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000530997-229300_30488.333333333333332134.0Nucleotide bindingGTP
HgeneNINchr14:51273455chr14:50292673ENST00000530997-229420_42388.333333333333332134.0Nucleotide bindingGTP
TgeneNEMFchr14:51273455chr14:50292673ENST000002983101433296_359496.01077.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST000002983101433483_514496.01077.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST000005457731332296_359454.01035.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST000005460461432296_359496.01056.0Coiled coilOntology_term=ECO:0000255
TgeneNEMFchr14:51273455chr14:50292673ENST000005460461432483_514496.01056.0Coiled coilOntology_term=ECO:0000255


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Fusion Protein-Protein Interaction


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 from validated records (BIOGRID-3.4.160)
GenePPI interactors
NINNIN, PRKACA, AURKA, GSK3B, AMOT, ELAVL1, LATS2, CEP170, CCDC68, TMOD1, CASQ2, C17orf59, CEP63, MED4, HERC2, OFD1, CEP128, CNTRL, ACTR1A, ANLN, AP3D1, CEP131, BAIAP2, CAMK2D, CC2D1A, CCDC138, CCNB1, CCNB2, CENPE, CEP164, CEP350, CKAP2, CLASP1, CLASP2, CSPP1, DBT, DCTN1, DCTN2, DHX35, DIAPH3, DYNC1H1, DYNC1I2, DYNC1LI1, DYNC1LI2, ECH1, EIF4ENIF1, ERC1, FAM83B, FGFR1OP, GPATCH1, HAUS1, HAUS3, HAUS4, HAUS5, HAUS6, HAUS7, HAUS8, HECTD1, HMMR, IQCB1, KIAA1671, KIF14, LUZP1, MAP7D3, MGA, NCKAP5L, NEDD1, NME7, PALLD, PCM1, PLK1, RASSF8, RLTPR, SAMD4B, SDCCAG3, SPC24, SVIL, TJP1, TNRC6B, TP53, TP53BP2, TTC28, TTF2, TTK, TXLNA, UNC45A, UPF1, WDR83, ACTR2, AHCY, ARPC3, CEP192, CSNK1A1, HMGN3, ISOC1, PIBF1, PMPCB, RAB2A, SSX2IP, TCHP, YWHAH, POC5, KIAA1244, NHP2L1, BAX, MYH13, DOT1L, Cep131, Wdr61, Fus, CDC14A, SYCE3, TCP10L, ZNF331, COG5, EGLN3, RBM10, GTSE1, YWHAE, KLC1, KIAA1429, DYNC1I1, APRT, DSG2, EIF6, ERLIN1, FLOT2, GANAB, GCAT, GNAI3, GSK3A, HUS1, LIPA, MCU, MEN1, MIA3, MRPL41, MSTO1, PCID2, PKP4, PRIM1, PUS1, RAB3B, RFC5, RPL35, SENP1, SLC25A15, STXBP3, TIMM44, TMEM165, TUBA1C, ATP6V1H, ANXA2, IQGAP1, ESYT2, ATP1A1, NUP93, NUP205, SLC25A4, CEP55, WDR3, MYO1D, DNAJB6, LMNB1, PLOD1, AGRN, RPL7, KRT5, NOMO2, GFPT1, ARHGEF2, PRDX4, ACOT9, MCM3, TAF2, LONP1, PFKM, DHX40, FLOT1, MTPAP, PPM1F, RBM14, TUBB6, ARCN1, DNAJA3, LTBP4, TUBB4A, AASS, XIAP, TSFM, ETFA, GTPBP1, GCLM, BICD1, ACTR10, C1orf198, C2CD3, C5orf42, CCDC14, CCDC22, CCDC57, CCDC66, CCDC77, CCDC85C, CCHCR1, CENPJ, CEP135, CEP152, CEP162, CEP170B, CEP250, CEP290, CEP295, CEP85L, CEP95, CGNL1, CIAPIN1, DCTN3, DCTN4, EIF4E2, FAM184A, FAM83G, FOPNL, GRN, ICK, IFFO2, KIF7, KIZ, LATS1, LCA5, LRRCC1, C17orf104, MZT2B, NDE1, ODF2, PDZRN3, PLEKHG1, PPP1R13B, PPP2R3A, PROSER3, PXN, RNF135, RPGRIP1L, SASS6, SCLT1, SPATA2, STIL, TBC1D5, TBKBP1, TEX9, TTC30A, TTLL5, TUBGCP2, TXLNG, WRAP73, YTHDF2, ALMS1, PCNT, SIPA1L3, CYLD, ANKRD26, TBC1D31, FAM83H, USP54, SPAG5, IFT81, LIMD1, CAMSAP1, BACH2, SIPA1L2, CKAP5, INA, GIGYF2, TANC1, CEP97, CTTN, CAMSAP3, HAUS2, ARHGAP21, CAPZB, CAMSAP2, VCPIP1, TTC26, XRN1, EIF4G2, SMG7, RINT1, APC, IFT74, TNRC6A, MIB1, ANKHD1-EIF4EBP3, TBK1, SIPA1L1, NDC80, BRCA2, IFT46, PRKACB, EXOC4, KRT8, L3MBTL2, TRIO, KNSTRN, DPYSL2, PSMC2, KRT19, BICD2, KIAA1217, ZNF598, CAPZA1, nsp13, C14orf166, AUNIP, HIST1H1A, CIT, KIF23, TRIM33, nsp13ab, ORF6, DNAJB5, KDM1A, KRT18, MLLT4, SEPT10, SYNE3, VPS33A, VPS33B, CEP170P1, C15orf59, PIP, ARSE, CCDC96, NUP62, KXD1, WHAMMP3, SNRPC, MBD3L2, PTP4A3, KRT38, SGCA, SERINC2, RNF185, MRPL38, SKA3, APLNR, CCDC51, SNW1, PRPF6, UTP14A,


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
NINall structure
NEMF


check button - Retained interactions in fusion protein (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenStill interaction with


check button - Lost interactions due to fusion (protein functional feature from UniProt).
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenInteraction lost with


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Related Drugs to NIN-NEMF


check button Drugs used for this fusion-positive patient.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDrugSourcePMID

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Related Diseases to NIN-NEMF


check button Diseases that have this fusion gene.
(Manual curation of PubMed, 04-30-2022 + MyCancerGenome)
HgeneTgeneDiseaseSourcePMID

check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneNINC3553870SECKEL SYNDROME 72GENOMICS_ENGLAND;ORPHANET;UNIPROT