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MYMX (myomixer, myoblast fusion factor)

Identity

Alias (NCBI)MINION
hMINION
HGNC (Hugo) MYMX
HGNC Alias symbMINION
HGNC Alias namemicroprotein inducer of fusion
 myomerger
LocusID (NCBI) 101929726
Atlas_Id 57049
Location 6p21.1  [Link to chromosome band 6p21]
Location_base_pair Starts at 44216926 and ends at 44218234 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
Note

Non-annotated gene. Preliminary data : if you are an author
who wish to write a full paper/card on this gene, go to  How to contribute



External links

Nomenclature
HGNC (Hugo)MYMX   52391
Cards
Entrez_Gene (NCBI)MYMX  101929726  myomixer, myoblast fusion factor
AliasesMINION; hMINION
GeneCards (Weizmann)MYMX
Ensembl hg19 (Hinxton)ENSG00000262179 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000262179 [Gene_View]  ENSG00000262179 [Sequence]  chr6:44216926-44218234 [Contig_View]  MYMX [Vega]
ICGC DataPortalENSG00000262179
TCGA cBioPortalMYMX
AceView (NCBI)MYMX
Genatlas (Paris)MYMX
WikiGenes101929726
SOURCE (Princeton)MYMX
Genetics Home Reference (NIH)MYMX
Genomic and cartography
GoldenPath hg38 (UCSC)MYMX  -     chr6:44216926-44218234 +  6p21.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)MYMX  -     6p21.1   [Description]    (hg19-Feb_2009)
GoldenPathMYMX - 6p21.1 [CytoView hg19]  MYMX - 6p21.1 [CytoView hg38]
ImmunoBaseENSG00000262179
genome Data Viewer NCBIMYMX [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AA501523 AI286144 BX107578 KY857877
RefSeq transcript (Entrez)NM_001315494 NM_001347931
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)MYMX
Alternative Splicing GalleryENSG00000262179
Gene ExpressionMYMX [ NCBI-GEO ]   MYMX [ EBI - ARRAY_EXPRESS ]   MYMX [ SEEK ]   MYMX [ MEM ]
Gene Expression Viewer (FireBrowse)MYMX [ Firebrowse - Broad ]
GenevisibleExpression of MYMX in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)101929726
GTEX Portal (Tissue expression)MYMX
Human Protein AtlasENSG00000262179-MYMX [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)MYMX
DMDM Disease mutations101929726
Blocks (Seattle)MYMX
Human Protein Atlas [tissue]ENSG00000262179-MYMX [tissue]
Protein Interaction databases
FunCoupENSG00000262179
BioGRIDMYMX
STRING (EMBL)MYMX
ZODIACMYMX
Ontologies - Pathways
Huge Navigator MYMX [HugePedia]
snp3D : Map Gene to Disease101929726
BioCentury BCIQMYMX
ClinGenMYMX
Clinical trials, drugs, therapy
Protein Interactions : CTD101929726
Pharm GKB GenePA166181577
Clinical trialMYMX
Miscellaneous
canSAR (ICR)MYMX (select the gene name)
HarmonizomeMYMX
DataMed IndexMYMX
Probes
Litterature
PubMed5 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineMYMX
EVEXMYMX
GoPubMedMYMX
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 14 14:23:19 CEST 2020

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