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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: 32601

FusionGeneSummary for SAMD9_GCLM

check button Fusion gene summary
Fusion gene informationFusion gene name: SAMD9_GCLM
Fusion gene ID: 32601
HgeneTgene
Gene symbol

SAMD9

GCLM

Gene ID

54809

2730

Gene namesterile alpha motif domain containing 9glutamate-cysteine ligase modifier subunit
SynonymsC7orf5|DRIF1|MIRAGE|NFTC|OEF1|OEF2GLCLR
Cytomap

7q21.2

1p22.1

Type of geneprotein-codingprotein-coding
Descriptionsterile alpha motif domain-containing protein 9SAM domain-containing protein 9expressed in aggressive fibromatosisglutamate--cysteine ligase regulatory subunitGCS light chainGSC light chaingamma-ECS regulatory subunitgamma-glutamylcysteine synthetase regulatory subunitglutamate-cysteine ligase (gamma-glutamylcysteine synthetase), regulatory (30.8kD)glutamate-cy
Modification date2018052320180523
UniProtAcc

Q5K651

P48507

Ensembl transtripts involved in fusion geneENST00000379958, ENST00000370238, 
ENST00000467772, 
Fusion gene scores* DoF score2 X 2 X 2=83 X 3 X 2=18
# samples 23
** MAII scorelog2(2/8*10)=1.32192809488736log2(3/18*10)=0.736965594166206
effective Gene in Pan-Cancer Fusion Genes (eGinPCFGs).
DoF>8 and MAII>0
Context

PubMed: SAMD9 [Title/Abstract] AND GCLM [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
HgeneSAMD9

GO:0034058

endosomal vesicle fusion

24029230

TgeneGCLM

GO:0006536

glutamate metabolic process

9841880|9895302

TgeneGCLM

GO:0006750

glutathione biosynthetic process

10395918

TgeneGCLM

GO:0006979

response to oxidative stress

10395918

TgeneGCLM

GO:0042493

response to drug

9895302


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
ChiTaRS3.1AI133413SAMD9chr7

92730629

+GCLMchr1

94354110

-
* 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-3UTRENST00000379958ENST00000370238SAMD9chr7

92730629

+GCLMchr1

94354110

-
intron-intronENST00000379958ENST00000467772SAMD9chr7

92730629

+GCLMchr1

94354110

-

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FusionProtFeatures for SAMD9_GCLM


check buttonMain function of each fusion partner protein. (from UniProt)
HgeneTgene
SAMD9

Q5K651

GCLM

P48507

May play a role in the inflammatory response to tissueinjury and the control of extra-osseous calcification, acting as adownstream target of TNF-alpha signaling. Involved in theregulation of EGR1, in coordination with RGL2. May be involved inendosome fusion. {ECO:0000269|PubMed:16960814,ECO:0000269|PubMed:18094730, ECO:0000269|PubMed:21160498,ECO:0000269|PubMed:24029230}.

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 SAMD9_GCLM


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 SAMD9_GCLM


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 SAMD9_GCLM


check button Drugs targeting genes involved in this fusion gene.
(DrugBank Version 5.1.0 2018-04-02)
PartnerGeneUniProtAccDrugBank IDDrug nameDrug activityDrug typeDrug status
TgeneGCLMP48507DB00142Glutamic AcidGlutamate--cysteine ligase regulatory subunitsmall moleculeapproved|nutraceutical

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RelatedDiseases for SAMD9_GCLM


check button Diseases associated with fusion partners.
(DisGeNet 4.0)
PartnerGeneDisease IDDisease name# pubmedsSource
HgeneSAMD9C0015934Fetal Growth Retardation1CTD_human
HgeneSAMD9C0021400Influenza1CTD_human
HgeneSAMD9C0021831Intestinal Diseases1CTD_human
HgeneSAMD9C0042063Urogenital Abnormalities1CTD_human
HgeneSAMD9C0220766Congenital hypoplasia of adrenal gland1CTD_human
HgeneSAMD9C1864861Tumoral Calcinosis, Normophosphatemic, Familial1CTD_human;ORPHANET;UNIPROT
HgeneSAMD9C3463824MYELODYSPLASTIC SYNDROME1CTD_human
HgeneSAMD9C3714514Infection1CTD_human
TgeneGCLMC0036341Schizophrenia3PSYGENET
TgeneGCLMC0027051Myocardial Infarction2CTD_human
TgeneGCLMC0005138Berylliosis1CTD_human
TgeneGCLMC0033937Psychoses, Drug1PSYGENET
TgeneGCLMC0036351Residual schizophrenia1PSYGENET
TgeneGCLMC0036939Shared Paranoid Disorder1PSYGENET