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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: 9216

FusionGeneSummary for D2HGDH_MLPH

check button Fusion gene summary
Fusion gene informationFusion gene name: D2HGDH_MLPH
Fusion gene ID: 9216
HgeneTgene
Gene symbol

D2HGDH

MLPH

Gene ID

728294

79083

Gene nameD-2-hydroxyglutarate dehydrogenasemelanophilin
SynonymsD2HGDSLAC2-A
Cytomap

2q37.3

2q37.3

Type of geneprotein-codingprotein-coding
DescriptionD-2-hydroxyglutarate dehydrogenase, mitochondrialmelanophilinexophilin-3slp homolog lacking C2 domains asynaptotagmin-like protein 2a
Modification date2018052320180523
UniProtAcc

Q8N465

Q9BV36

Ensembl transtripts involved in fusion geneENST00000537090, ENST00000321264, 
ENST00000403782, ENST00000342518, 
ENST00000486953, 
ENST00000410032, 
ENST00000264605, ENST00000445024, 
ENST00000468178, ENST00000338530, 
ENST00000409373, 
Fusion gene scores* DoF score3 X 3 X 3=276 X 6 X 4=144
# samples 36
** MAII scorelog2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
log2(6/144*10)=-1.26303440583379
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
Context

PubMed: D2HGDH [Title/Abstract] AND MLPH [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
TCGALDESCATCGA-2H-A9GR-01AD2HGDHchr2

242684359

+MLPHchr2

238463348

+
* 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
intron-intronENST00000537090ENST00000410032D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-3UTRENST00000537090ENST00000264605D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000537090ENST00000445024D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000537090ENST00000468178D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000537090ENST00000338530D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000537090ENST00000409373D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000321264ENST00000410032D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-3UTRENST00000321264ENST00000264605D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000321264ENST00000445024D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000321264ENST00000468178D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000321264ENST00000338530D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000321264ENST00000409373D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000403782ENST00000410032D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-3UTRENST00000403782ENST00000264605D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000403782ENST00000445024D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000403782ENST00000468178D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000403782ENST00000338530D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000403782ENST00000409373D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000342518ENST00000410032D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-3UTRENST00000342518ENST00000264605D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000342518ENST00000445024D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000342518ENST00000468178D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000342518ENST00000338530D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000342518ENST00000409373D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000486953ENST00000410032D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-3UTRENST00000486953ENST00000264605D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000486953ENST00000445024D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000486953ENST00000468178D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000486953ENST00000338530D2HGDHchr2

242684359

+MLPHchr2

238463348

+
intron-intronENST00000486953ENST00000409373D2HGDHchr2

242684359

+MLPHchr2

238463348

+

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FusionProtFeatures for D2HGDH_MLPH


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
D2HGDH

Q8N465

MLPH

Q9BV36

Catalyzes the oxidation of D-2-hydroxyglutarate toalpha-ketoglutarate. {ECO:0000269|PubMed:15070399}. Rab effector protein involved in melanosome transport.Serves as link between melanosome-bound RAB27A and the motorprotein MYO5A. {ECO:0000269|PubMed:12062444}.

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 D2HGDH_MLPH


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 D2HGDH_MLPH


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
D2HGDHDHRS4L2, TBCB, STK11, ZNF462, RAB30, SDHB, SLAMF1, TRMT1, YBEY, P2RX2, CD79B, GATCMLPHRAB27A, MYO5A, ACTA1, RAB27B, RAB10, CUL2, 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 D2HGDH_MLPH


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 D2HGDH_MLPH


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneD2HGDHC3152055D-2-HYDROXYGLUTARIC ACIDURIA 13ORPHANET;UNIPROT
HgeneD2HGDHC0002514Amino Acid Metabolism, Inborn Errors1CTD_human
TgeneMLPHC1836573GRISCELLI SYNDROME, TYPE 31CTD_human;ORPHANET;UNIPROT