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LOC102546229 (uncharacterized LOC102546229)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 102546229
Atlas_Id 67664
Location 5q31.1  [Link to chromosome band 5q31]
Location_base_pair Starts at 134429051 and ends at 134435047 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)LOC102546229  102546229  uncharacterized LOC102546229
Aliases
GeneCards (Weizmann)LOC102546229
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr5:134429051-134435047 [Contig_View]  LOC102546229 [Vega]
TCGA cBioPortalLOC102546229
AceView (NCBI)LOC102546229
Genatlas (Paris)LOC102546229
WikiGenes102546229
SOURCE (Princeton)LOC102546229
Genetics Home Reference (NIH)LOC102546229
Genomic and cartography
GoldenPath hg38 (UCSC)LOC102546229  -     chr5:134429051-134435047 -  5q31.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC102546229  -     5q31.1   [Description]    (hg19-Feb_2009)
EnsemblLOC102546229 - 5q31.1 [CytoView hg19]  LOC102546229 - 5q31.1 [CytoView hg38]
Mapping of homologs : NCBILOC102546229 [Mapview hg19]  LOC102546229 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BU621598 CV379430
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC102546229
Gene ExpressionLOC102546229 [ NCBI-GEO ]   LOC102546229 [ EBI - ARRAY_EXPRESS ]   LOC102546229 [ SEEK ]   LOC102546229 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC102546229 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102546229
GTEX Portal (Tissue expression)LOC102546229
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC102546229
DMDM Disease mutations102546229
Blocks (Seattle)LOC102546229
Protein Interaction databases
BioGRIDLOC102546229
STRING (EMBL)LOC102546229
ZODIACLOC102546229
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease102546229
BioCentury BCIQLOC102546229
ClinGenLOC102546229
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102546229
Clinical trialLOC102546229
Miscellaneous
canSAR (ICR)LOC102546229 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC102546229
EVEXLOC102546229
GoPubMedLOC102546229
iHOPLOC102546229
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 13:52:40 CET 2017

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