Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101241902 (chromosome 4 open reading frame 46 pseudogene)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101241902
Atlas_Id 66997
Location 8q21.13  [Link to chromosome band 8q21]
Location_base_pair Starts at 78722848 and ends at 78724374 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)LOC101241902  101241902  chromosome 4 open reading frame 46 pseudogene
Aliases
GeneCards (Weizmann)LOC101241902
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr8:78722848-78724374 [Contig_View]  LOC101241902 [Vega]
TCGA cBioPortalLOC101241902
AceView (NCBI)LOC101241902
Genatlas (Paris)LOC101241902
WikiGenes101241902
SOURCE (Princeton)LOC101241902
Genetics Home Reference (NIH)LOC101241902
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101241902  -     chr8:78722848-78724374 -  8q21.13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101241902  -     8q21.13   [Description]    (hg19-Feb_2009)
EnsemblLOC101241902 - 8q21.13 [CytoView hg19]  LOC101241902 - 8q21.13 [CytoView hg38]
Mapping of homologs : NCBILOC101241902 [Mapview hg19]  LOC101241902 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC072451
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101241902
Cluster EST : UnigeneHs.388511 [ NCBI ]
CGAP (NCI)Hs.388511
Gene ExpressionLOC101241902 [ NCBI-GEO ]   LOC101241902 [ EBI - ARRAY_EXPRESS ]   LOC101241902 [ SEEK ]   LOC101241902 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101241902 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101241902
GTEX Portal (Tissue expression)LOC101241902
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101241902
DMDM Disease mutations101241902
Blocks (Seattle)LOC101241902
Protein Interaction databases
BioGRIDLOC101241902
STRING (EMBL)LOC101241902
ZODIACLOC101241902
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101241902
BioCentury BCIQLOC101241902
ClinGenLOC101241902
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101241902
Clinical trialLOC101241902
Miscellaneous
canSAR (ICR)LOC101241902 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101241902
EVEXLOC101241902
GoPubMedLOC101241902
iHOPLOC101241902
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 : Tue Nov 21 13:49:28 CET 2017

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