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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: 22161

FusionGeneSummary for MLLT1_PRLR

check button Fusion gene summary
Fusion gene informationFusion gene name: MLLT1_PRLR
Fusion gene ID: 22161
HgeneTgene
Gene symbol

MLLT1

PRLR

Gene ID

4298

5618

Gene nameMLLT1, super elongation complex subunitprolactin receptor
SynonymsENL|LTG19|YEATS1HPRL|MFAB|RI-PRLR|hPRLrI
Cytomap

19p13.3

5p13.2

Type of geneprotein-codingprotein-coding
Descriptionprotein ENLCTC-503J8.6ENL/MLL fusionMLL/ENL fusion proteinMLLT1/MLL fusionYEATS domain-containing protein 1myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog); translocated to, 1myeloid/lymphoid or mixed-lineage leukemia (trithorax homolprolactin receptorhPRL receptorsecreted prolactin binding protein
Modification date2018051920180523
UniProtAcc

Q03111

P16471

Ensembl transtripts involved in fusion geneENST00000252674, ENST00000585588, 
ENST00000342362, ENST00000382002, 
ENST00000231423, ENST00000513753, 
ENST00000397391, ENST00000348262, 
ENST00000542609, ENST00000310101, 
ENST00000511486, ENST00000509934, 
Fusion gene scores* DoF score6 X 8 X 4=1926 X 5 X 4=120
# samples 96
** MAII scorelog2(9/192*10)=-1.09310940439148
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(6/120*10)=-1
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: MLLT1 [Title/Abstract] AND PRLR [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
TgenePRLR

GO:0007171

activation of transmembrane receptor protein tyrosine kinase activity

10585417


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
TCGARVACCTCGA-OR-A5K9-01AMLLT1chr19

6270590

-PRLRchr5

35118224

-
* 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
5CDS-5UTRENST00000252674ENST00000342362MLLT1chr19

6270590

-PRLRchr5

35118224

-
5CDS-5UTRENST00000252674ENST00000382002MLLT1chr19

6270590

-PRLRchr5

35118224

-
5CDS-intronENST00000252674ENST00000231423MLLT1chr19

6270590

-PRLRchr5

35118224

-
5CDS-intronENST00000252674ENST00000513753MLLT1chr19

6270590

-PRLRchr5

35118224

-
5CDS-intronENST00000252674ENST00000397391MLLT1chr19

6270590

-PRLRchr5

35118224

-
5CDS-intronENST00000252674ENST00000348262MLLT1chr19

6270590

-PRLRchr5

35118224

-
5CDS-intronENST00000252674ENST00000542609MLLT1chr19

6270590

-PRLRchr5

35118224

-
5CDS-intronENST00000252674ENST00000310101MLLT1chr19

6270590

-PRLRchr5

35118224

-
5CDS-intronENST00000252674ENST00000511486MLLT1chr19

6270590

-PRLRchr5

35118224

-
5CDS-intronENST00000252674ENST00000509934MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-5UTRENST00000585588ENST00000342362MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-5UTRENST00000585588ENST00000382002MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-intronENST00000585588ENST00000231423MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-intronENST00000585588ENST00000513753MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-intronENST00000585588ENST00000397391MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-intronENST00000585588ENST00000348262MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-intronENST00000585588ENST00000542609MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-intronENST00000585588ENST00000310101MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-intronENST00000585588ENST00000511486MLLT1chr19

6270590

-PRLRchr5

35118224

-
intron-intronENST00000585588ENST00000509934MLLT1chr19

6270590

-PRLRchr5

35118224

-

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FusionProtFeatures for MLLT1_PRLR


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
MLLT1

Q03111

PRLR

P16471

Component of the super elongation complex (SEC), acomplex required to increase the catalytic rate of RNA polymeraseII transcription by suppressing transient pausing by thepolymerase at multiple sites along the DNA.{ECO:0000269|PubMed:20159561, ECO:0000269|PubMed:20471948}.

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 MLLT1_PRLR


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 MLLT1_PRLR


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
MLLT1CBX8, AFF1, CDK9, WDR5, DOT1L, MLLT3, RFX5, AFF4, CSNK2A1, BCOR, RFXAP, MLLT10, ACACA, CHD1, ELL, SIRT1, MLLT6, CCNT1, KMT2A, BRD4, ELL2, PAF1, POLR2A, MED26, HIST3H3, HIST1H1B, EAF1, ELL3, RNF2, RPL12, MRPL12, HIST2H2AC, H2AFX, HIST2H2BE, HIST4H4, BMI1, PIP4K2A, EPB41L2, CAMKV, BPIFB1, YAF2, RYBP, DENND2D, ARRB2, TRIM25PRLRPPIA, SOCS3, TEC, VAV1, SOCS2, JAK2, PTPN11, GTF3A, FBXW11, CREBBP, PRLR, STAT5B, BTRC


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 MLLT1_PRLR


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgenePRLRP16471DB01185FluoxymesteroneProlactin receptorsmall moleculeapproved|illicit
TgenePRLRP16471DB00052SomatotropinProlactin receptorbiotechapproved|investigational

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RelatedDiseases for MLLT1_PRLR


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
TgenePRLRC0024667Animal Mammary Neoplasms2CTD_human
TgenePRLRC0000786Spontaneous abortion1CTD_human
TgenePRLRC0004352Autistic Disorder1CTD_human
TgenePRLRC0014175Endometriosis1CTD_human
TgenePRLRC0020514Hyperprolactinemia1HPO;ORPHANET;UNIPROT
TgenePRLRC0023893Liver Cirrhosis, Experimental1CTD_human
TgenePRLRC0024668Mammary Neoplasms, Experimental1CTD_human
TgenePRLRC3809918MULTIPLE FIBROADENOMAS OF THE BREAST1ORPHANET;UNIPROT