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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: 22057

FusionGeneSummary for MITF_MORC1

check button Fusion gene summary
Fusion gene informationFusion gene name: MITF_MORC1
Fusion gene ID: 22057
HgeneTgene
Gene symbol

MITF

MORC1

Gene ID

4286

27136

Gene namemelanogenesis associated transcription factorMORC family CW-type zinc finger 1
SynonymsCMM8|COMMAD|MI|WS2|WS2A|bHLHe32CT33|MORC|ZCW6
Cytomap

3p13

3q13.13

Type of geneprotein-codingprotein-coding
Descriptionmicrophthalmia-associated transcription factorclass E basic helix-loop-helix protein 32microphtalmia-associated transcription factorMORC family CW-type zinc finger protein 1cancer/testis antigen 33microrchidia, mouse, homolog of
Modification date2018052720180523
UniProtAcc

O75030

Q86VD1

Ensembl transtripts involved in fusion geneENST00000352241, ENST00000448226, 
ENST00000472437, ENST00000328528, 
ENST00000314589, ENST00000394355, 
ENST00000314557, ENST00000394351, 
ENST00000531774, ENST00000394348, 
ENST00000232603, ENST00000483760, 
Fusion gene scores* DoF score7 X 3 X 3=633 X 3 X 3=27
# samples 53
** MAII scorelog2(5/63*10)=-0.333423733725192
possibly effective Gene in Pan-Cancer Fusion Genes (peGinPCFGs).
DoF>8 and MAII<0
log2(3/27*10)=0.15200309344505
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: MITF [Title/Abstract] AND MORC1 [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
HgeneMITF

GO:0010628

positive regulation of gene expression

22234890

HgeneMITF

GO:0045893

positive regulation of transcription, DNA-templated

9647758

HgeneMITF

GO:0045944

positive regulation of transcription by RNA polymerase II

20530484|21209915

HgeneMITF

GO:0065003

protein-containing complex assembly

20530484

HgeneMITF

GO:2000144

positive regulation of DNA-templated transcription, initiation

8995290|12204775

HgeneMITF

GO:2001141

regulation of RNA biosynthetic process

16411896


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
TCGALDSKCMTCGA-WE-A8ZX-06AMITFchr3

69928534

+MORC1chr3

108788604

-
* 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
Frame-shitENST00000352241ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000352241ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000448226ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000448226ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000472437ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000472437ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000328528ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000328528ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000314589ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000314589ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000394355ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
Frame-shitENST00000394355ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-
intron-3CDSENST00000314557ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
intron-3CDSENST00000314557ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-
intron-3CDSENST00000394351ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
intron-3CDSENST00000394351ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-
intron-3CDSENST00000531774ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
intron-3CDSENST00000531774ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-
intron-3CDSENST00000394348ENST00000232603MITFchr3

69928534

+MORC1chr3

108788604

-
intron-3CDSENST00000394348ENST00000483760MITFchr3

69928534

+MORC1chr3

108788604

-

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FusionProtFeatures for MITF_MORC1


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

O75030

MORC1

Q86VD1

Required for spermatogenesis.{ECO:0000250|UniProtKB:Q9WVL5}.

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 MITF_MORC1


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 MITF_MORC1


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
MITFLEF1, PIAS3, PATZ1, UBE2I, TFE3, FOS, SPI1, PAX6, TFEC, SUMO1, PIAS1, PIAS2, PSMD14, MARK3, CDK2, ELAVL1, HINT1, APP, EPAS1, STUB1, HK3, EBP, EP300, XPO1, TFEB, RBM6, KLHL20, TRIM25MORC1MORC2, RNF40, HERC1, PJA1, GMEB1


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 MITF_MORC1


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 MITF_MORC1


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneMITFC3152204MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 82CTD_human;ORPHANET;UNIPROT
HgeneMITFC0007134Renal Cell Carcinoma1CTD_human
HgeneMITFC0007621Neoplastic Cell Transformation1CTD_human
HgeneMITFC0011053Deafness1CTD_human
HgeneMITFC0025202melanoma1CTD_human;HPO
HgeneMITFC0078918Albinism, Oculocutaneous1CTD_human
HgeneMITFC0151779Cutaneous Melanoma1CTD_human
HgeneMITFC0391816Tietz syndrome1CTD_human;ORPHANET;UNIPROT
HgeneMITFC0549567Pigmentation Disorders1CTD_human
HgeneMITFC1860339WAARDENBURG SYNDROME, TYPE IIA1CTD_human;UNIPROT
HgeneMITFC2700265Waardenburg Syndrome Type 21CTD_human;ORPHANET
TgeneMORC1C0041696Unipolar Depression1PSYGENET
TgeneMORC1C1269683Major Depressive Disorder1PSYGENET