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LOC392452 (mitochondrial fission factor pseudogene)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 392452
Atlas_Id 68110
Location Xp11.3  [Link to chromosome band Xp11]
Location_base_pair Starts at 45731088 and ends at 45731757 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC392452  392452  mitochondrial fission factor pseudogene
Aliases
GeneCards (Weizmann)LOC392452
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chrX:45731088-45731757 [Contig_View]  LOC392452 [Vega]
TCGA cBioPortalLOC392452
AceView (NCBI)LOC392452
Genatlas (Paris)LOC392452
WikiGenes392452
SOURCE (Princeton)LOC392452
Genetics Home Reference (NIH)LOC392452
Genomic and cartography
GoldenPath hg38 (UCSC)LOC392452  -     chrX:45731088-45731757 +  Xp11.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC392452  -     Xp11.3   [Description]    (hg19-Feb_2009)
EnsemblLOC392452 - Xp11.3 [CytoView hg19]  LOC392452 - Xp11.3 [CytoView hg38]
Mapping of homologs : NCBILOC392452 [Mapview hg19]  LOC392452 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BI559448 BX098273
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC392452
Cluster EST : UnigeneHs.745266 [ NCBI ]
CGAP (NCI)Hs.745266
Gene ExpressionLOC392452 [ NCBI-GEO ]   LOC392452 [ EBI - ARRAY_EXPRESS ]   LOC392452 [ SEEK ]   LOC392452 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC392452 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)392452
GTEX Portal (Tissue expression)LOC392452
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC392452
DMDM Disease mutations392452
Blocks (Seattle)LOC392452
Protein Interaction databases
BioGRIDLOC392452
STRING (EMBL)LOC392452
ZODIACLOC392452
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease392452
BioCentury BCIQLOC392452
ClinGenLOC392452
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD392452
Clinical trialLOC392452
Miscellaneous
canSAR (ICR)LOC392452 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC392452
EVEXLOC392452
GoPubMedLOC392452
iHOPLOC392452
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Nov 20 19:53:21 CET 2017

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