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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: 15812

FusionGeneSummary for HADH_MEIS1

check button Fusion gene summary
Fusion gene informationFusion gene name: HADH_MEIS1
Fusion gene ID: 15812
HgeneTgene
Gene symbol

HADH

MEIS1

Gene ID

3033

4211

Gene namehydroxyacyl-CoA dehydrogenaseMeis homeobox 1
SynonymsHAD|HADH1|HADHSC|HCDH|HHF4|MSCHAD|SCHAD-
Cytomap

4q25

2p14

Type of geneprotein-codingprotein-coding
Descriptionhydroxyacyl-coenzyme A dehydrogenase, mitochondrialL-3-hydroxyacyl-Coenzyme A dehydrogenase, short chainmedium and short-chain L-3-hydroxyacyl-coenzyme A dehydrogenaseshort-chain 3-hydroxyacyl-CoA dehydrogenasetestis secretory sperm-binding protein Lihomeobox protein Meis1Meis1, myeloid ecotropic viral integration site 1 homologWUGSC:H_NH0444B04.1leukemogenic homolog protein
Modification date2018051920180523
UniProtAcc

Q16836

O00470

Ensembl transtripts involved in fusion geneENST00000603302, ENST00000403312, 
ENST00000309522, ENST00000505878, 
ENST00000454409, ENST00000510728, 
ENST00000560281, ENST00000407092, 
ENST00000272369, ENST00000488550, 
ENST00000398506, ENST00000444274, 
ENST00000495021, ENST00000409517, 
Fusion gene scores* DoF score6 X 5 X 3=903 X 3 X 2=18
# samples 73
** MAII scorelog2(7/90*10)=-0.362570079384708
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: HADH [Title/Abstract] AND MEIS1 [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
ChiTaRS3.1BM504479HADHchr4

108935744

+MEIS1chr2

66784099

+
* 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-intronENST00000603302ENST00000560281HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000603302ENST00000407092HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000603302ENST00000272369HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000603302ENST00000488550HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000603302ENST00000398506HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000603302ENST00000444274HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000603302ENST00000495021HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000603302ENST00000409517HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000403312ENST00000560281HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000403312ENST00000407092HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000403312ENST00000272369HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000403312ENST00000488550HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000403312ENST00000398506HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000403312ENST00000444274HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000403312ENST00000495021HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000403312ENST00000409517HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000309522ENST00000560281HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000309522ENST00000407092HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000309522ENST00000272369HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000309522ENST00000488550HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000309522ENST00000398506HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000309522ENST00000444274HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000309522ENST00000495021HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000309522ENST00000409517HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000505878ENST00000560281HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000505878ENST00000407092HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000505878ENST00000272369HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000505878ENST00000488550HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000505878ENST00000398506HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000505878ENST00000444274HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000505878ENST00000495021HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000505878ENST00000409517HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000454409ENST00000560281HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000454409ENST00000407092HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000454409ENST00000272369HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000454409ENST00000488550HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000454409ENST00000398506HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000454409ENST00000444274HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000454409ENST00000495021HADHchr4

108935744

+MEIS1chr2

66784099

+
5CDS-intronENST00000454409ENST00000409517HADHchr4

108935744

+MEIS1chr2

66784099

+
intron-intronENST00000510728ENST00000560281HADHchr4

108935744

+MEIS1chr2

66784099

+
intron-intronENST00000510728ENST00000407092HADHchr4

108935744

+MEIS1chr2

66784099

+
intron-intronENST00000510728ENST00000272369HADHchr4

108935744

+MEIS1chr2

66784099

+
intron-intronENST00000510728ENST00000488550HADHchr4

108935744

+MEIS1chr2

66784099

+
intron-intronENST00000510728ENST00000398506HADHchr4

108935744

+MEIS1chr2

66784099

+
intron-intronENST00000510728ENST00000444274HADHchr4

108935744

+MEIS1chr2

66784099

+
intron-intronENST00000510728ENST00000495021HADHchr4

108935744

+MEIS1chr2

66784099

+
intron-intronENST00000510728ENST00000409517HADHchr4

108935744

+MEIS1chr2

66784099

+

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FusionProtFeatures for HADH_MEIS1


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

Q16836

MEIS1

O00470

Plays an essential role in the mitochondrial beta-oxidation of short chain fatty acids. Exerts it highest activitytoward 3-hydroxybutyryl-CoA. Acts as a transcriptional regulator of PAX6. Acts as atranscriptional activator of PF4 in complex with PBX1 or PBX2.Required for hematopoiesis, megakaryocyte lineage development andvascular patterning. May function as a cofactor for HOXA7 andHOXA9 in the induction of myeloid leukemias.{ECO:0000269|PubMed:12609849}.

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 HADH_MEIS1


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 HADH_MEIS1


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


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 HADH_MEIS1


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 HADH_MEIS1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneHADHC0028754Obesity1CTD_human
HgeneHADHC0032927Precancerous Conditions1CTD_human
HgeneHADHC1864948Hyperinsulinemic Hypoglycemia, Familial, 41CTD_human;ORPHANET;UNIPROT
TgeneMEIS1C0035258Restless Legs Syndrome1CTD_human
TgeneMEIS1C1458155Mammary Neoplasms1CTD_human