Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100506358 (uncharacterized LOC100506358)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506358
Atlas_Id 79207
Location 14q24.2  [Link to chromosome band 14q24]
Location_base_pair Starts at 69811777 and ends at 69815967 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)-   -
Cards
Entrez_Gene (NCBI)LOC100506358  100506358  uncharacterized LOC100506358
Aliases
GeneCards (Weizmann)LOC100506358
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr14:69811777-69815967 [Contig_View]  LOC100506358 [Vega]
TCGA cBioPortalLOC100506358
AceView (NCBI)LOC100506358
Genatlas (Paris)LOC100506358
WikiGenes100506358
SOURCE (Princeton)LOC100506358
Genetics Home Reference (NIH)LOC100506358
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506358  -     chr14:69811777-69815967 +  14q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506358  -     14q24.2   [Description]    (hg19-Feb_2009)
EnsemblLOC100506358 - 14q24.2 [CytoView hg19]  LOC100506358 - 14q24.2 [CytoView hg38]
Mapping of homologs : NCBILOC100506358 [Mapview hg19]  LOC100506358 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC041582 BG572285 BX161426
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506358
Gene ExpressionLOC100506358 [ NCBI-GEO ]   LOC100506358 [ EBI - ARRAY_EXPRESS ]   LOC100506358 [ SEEK ]   LOC100506358 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506358 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506358
GTEX Portal (Tissue expression)LOC100506358
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506358
DMDM Disease mutations100506358
Blocks (Seattle)LOC100506358
IPIIPI00103698   
Protein Interaction databases
BioGRIDLOC100506358
STRING (EMBL)LOC100506358
ZODIACLOC100506358
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506358
BioCentury BCIQLOC100506358
ClinGenLOC100506358
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506358
Clinical trialLOC100506358
Miscellaneous
canSAR (ICR)LOC100506358 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506358
EVEXLOC100506358
GoPubMedLOC100506358
iHOPLOC100506358
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 13:48:41 CET 2017

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jlhuret@AtlasGeneticsOncology.org.