UTHEALTH HOME    ABOUT SBMI    A-Z    WEBMAIL    INSIDE THE UNIVERSITY
FusionGDB Logo

Home

Download

Statistics

Examples

Help

Contact

Terms of Use

Center for Computational Systems Medicine level1
leaf

Fusion Gene Summary

leaf

Fusion Gene Sample Information

leaf

Fusion ORF Analysis

leaf

Fusion Amino Acid Sequences

leaf

Fusion Protein Functional Features

leaf

Fusion Protein-Protein Interaction

leaf

Related drugs with this fusion protein

leaf

Related disease with this fusion protein

Fusion Protein:NLK-SLC39A11

Fusion Protein Summary

check button Fusion gene summary
Fusion partner gene informationFusion gene name: NLK-SLC39A11
FusionPDB ID: 59357
FusionGDB2.0 ID: 59357
HgeneTgene
Gene symbol

NLK

SLC39A11

Gene ID

51701

201266

Gene namenemo like kinasesolute carrier family 39 member 11
Synonyms-C17orf26|ZIP-11|ZIP11
Cytomap

17q11.2

17q24.3-q25.1

Type of geneprotein-codingprotein-coding
Descriptionserine/threonine-protein kinase NLKzinc transporter ZIP11Zrt- and Irt-like protein 11solute carrier family 39 (metal ion transporter), member 11
Modification date2020031320200313
UniProtAcc

Q9UBE8

.
Ensembl transtripts involved in fusion geneENST idsENST00000407008, ENST00000582037, 
ENST00000583517, 
ENST00000579732, 
ENST00000579988, ENST00000255559, 
ENST00000542342, 
Fusion gene scores for assessment (based on all fusion genes of FusionGDB 2.0)* DoF score18 X 10 X 9=162024 X 14 X 9=3024
# samples 2029
** MAII scorelog2(20/1620*10)=-3.01792190799726
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(29/3024*10)=-3.38233333420614
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context (manual curation of fusion genes in FusionPDB)

PubMed: NLK [Title/Abstract] AND SLC39A11 [Title/Abstract] AND fusion [Title/Abstract]

Most frequent breakpoint (based on all fusion genes of FusionGDB 2.0)NLK(26449758)-SLC39A11(70944014), # samples:1
Anticipated loss of major functional domain due to fusion event.NLK-SLC39A11 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.
NLK-SLC39A11 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.
NLK-SLC39A11 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.
NLK-SLC39A11 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.
* 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
HgeneNLK

GO:0050821

protein stabilization

25512613


check buttonFusion gene breakpoints across NLK (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 SLC39A11 (3'-gene)
* Click on the image to open the UCSC genome browser with custom track showing this image in a new window.
all structure


Top

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
ChimerDB4Non-Cancer5373NNLKchr17

26449758

+SLC39A11chr17

70944014

-


Top

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)
ENST00000407008NLKchr1726449758+ENST00000255559SLC39A11chr1770944014-364313067182007429
ENST00000407008NLKchr1726449758+ENST00000542342SLC39A11chr1770944014-366313067182028436

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
ENST00000407008ENST00000255559NLKchr1726449758+SLC39A11chr1770944014-0.0249268060.97507316
ENST00000407008ENST00000542342NLKchr1726449758+SLC39A11chr1770944014-0.0350884760.9649115

Top

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

>59357_59357_1_NLK-SLC39A11_NLK_chr17_26449758_ENST00000407008_SLC39A11_chr17_70944014_ENST00000255559_length(amino acids)=429AA_BP=196
MSLCGARANAKMMAAYNGGTSAAAAGHHHHHHHHLPHLPPPHLHHHHHPQHHLHPGSAAAVHPVQQHTSSAAAAAAAAAAAAAMLNPGQQ
QPYFPSPAPGQAPGPAAAAPAQVQAAAAATVKAHHHQHSHHPQQQLDIEPDRPIGYGAFGVVWSVTDPRDGKRVALKKMPNVFQNLVSCK
RVFRELKMLCFFKHDNGAAEDPQTTLALNFGSTLMKKKSDPEGPALLFPESELSIRIDKSENGEAYQRKKAAATGLPEGPAVPVPSRGNL
AQPGGSSWRRIALLILAITIHNVPEGLAVGVGFGAIEKTASATFESARNLAIGIGIQNFPEGLAVSLPLRGAGFSTWRAFWYGQLSGMVE

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

>59357_59357_2_NLK-SLC39A11_NLK_chr17_26449758_ENST00000407008_SLC39A11_chr17_70944014_ENST00000542342_length(amino acids)=436AA_BP=196
MSLCGARANAKMMAAYNGGTSAAAAGHHHHHHHHLPHLPPPHLHHHHHPQHHLHPGSAAAVHPVQQHTSSAAAAAAAAAAAAAMLNPGQQ
QPYFPSPAPGQAPGPAAAAPAQVQAAAAATVKAHHHQHSHHPQQQLDIEPDRPIGYGAFGVVWSVTDPRDGKRVALKKMPNVFQNLVSCK
RVFRELKMLCFFKHDNGAAEDPQTTLALNFGSTLMKKKSDPEGPALLFPESELSIRIGRAGLLSDKSENGEAYQRKKAAATGLPEGPAVP
VPSRGNLAQPGGSSWRRIALLILAITIHNVPEGLAVGVGFGAIEKTASATFESARNLAIGIGIQNFPEGLAVSLPLRGAGFSTWRAFWYG

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

Top

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/chr17:26449758/chr17:70944014)
- 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
NLK

Q9UBE8

.
FUNCTION: Serine/threonine-protein kinase that regulates a number of transcription factors with key roles in cell fate determination. Positive effector of the non-canonical Wnt signaling pathway, acting downstream of WNT5A, MAP3K7/TAK1 and HIPK2. Negative regulator of the canonical Wnt/beta-catenin signaling pathway. Binds to and phosphorylates TCF7L2/TCF4 and LEF1, promoting the dissociation of the TCF7L2/LEF1/beta-catenin complex from DNA, as well as the ubiquitination and subsequent proteolysis of LEF1. Together these effects inhibit the transcriptional activation of canonical Wnt/beta-catenin target genes. Negative regulator of the Notch signaling pathway. Binds to and phosphorylates NOTCH1, thereby preventing the formation of a transcriptionally active ternary complex of NOTCH1, RBPJ/RBPSUH and MAML1. Negative regulator of the MYB family of transcription factors. Phosphorylation of MYB leads to its subsequent proteolysis while phosphorylation of MYBL1 and MYBL2 inhibits their interaction with the coactivator CREBBP. Other transcription factors may also be inhibited by direct phosphorylation of CREBBP itself. Acts downstream of IL6 and MAP3K7/TAK1 to phosphorylate STAT3, which is in turn required for activation of NLK by MAP3K7/TAK1. Upon IL1B stimulus, cooperates with ATF5 to activate the transactivation activity of C/EBP subfamily members. Phosphorylates ATF5 but also stabilizes ATF5 protein levels in a kinase-independent manner (PubMed:25512613). {ECO:0000250|UniProtKB:O54949, ECO:0000269|PubMed:12482967, ECO:0000269|PubMed:14960582, ECO:0000269|PubMed:15004007, ECO:0000269|PubMed:15764709, ECO:0000269|PubMed:20061393, ECO:0000269|PubMed:20118921, ECO:0000269|PubMed:20874444, ECO:0000269|PubMed:21454679, ECO:0000269|PubMed:25512613}.FUNCTION: Might normally function as a transcriptional repressor. EWS-fusion-proteins (EFPS) may play a role in the tumorigenic process. They may disturb gene expression by mimicking, or interfering with the normal function of CTD-POLII within the transcription initiation complex. They may also contribute to an aberrant activation of the fusion protein target genes.

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
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+211106_111196.0528.0Compositional biasNote=Poly-Ala
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+211115_119196.0528.0Compositional biasNote=Poly-Ala
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+21122_25196.0528.0Compositional biasNote=Poly-Ala
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+21127_34196.0528.0Compositional biasNote=Poly-His
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+21142_48196.0528.0Compositional biasNote=Poly-His
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+21171_83196.0528.0Compositional biasNote=Poly-Ala
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+211144_152196.0528.0Nucleotide bindingATP
TgeneSLC39A11chr17:26449758chr17:70944014ENST00000255559310194_214102.0336.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST00000255559310263_285102.0336.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST00000255559310290_307102.0336.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST00000255559310322_342102.0336.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST00000542342310194_214102.0343.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST00000542342310263_285102.0343.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST00000542342310290_307102.0343.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST00000542342310322_342102.0343.0TransmembraneHelical

- Not-retained protein feature among the 13 regional features.
PartnerGeneHbpTbpENSTStrandBPexonTotalExonProtein feature loci*BPlociTotalLenProtein featureProtein feature note
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+211138_427196.0528.0DomainProtein kinase
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+211298_300196.0528.0MotifNote=TQE
HgeneNLKchr17:26449758chr17:70944014ENST00000407008+211428_527196.0528.0RegionRequired for homodimerization and kinase activation and localization to the nucleus
TgeneSLC39A11chr17:26449758chr17:70944014ENST0000025555931012_32102.0336.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST0000025555931044_64102.0336.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST0000025555931072_92102.0336.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST0000054234231012_32102.0343.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST0000054234231044_64102.0343.0TransmembraneHelical
TgeneSLC39A11chr17:26449758chr17:70944014ENST0000054234231072_92102.0343.0TransmembraneHelical


Top

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


check button Protein-protein interactors based on sequence similarity (STRING)
GeneSTRING network
NLK
SLC39A11


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


Top

Related Drugs to NLK-SLC39A11


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

Top

Related Diseases to NLK-SLC39A11


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