Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC102724357 (uncharacterized LOC102724357)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 102724357
Atlas_Id 78043
Location 6q27  [Link to chromosome band 6q27]
Location_base_pair Starts at 169067786 and ends at 169069424 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)LOC102724357  102724357  uncharacterized LOC102724357
Aliases
GeneCards (Weizmann)LOC102724357
Ensembl hg19 (Hinxton)ENSG00000234519 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000234519 [Gene_View]  ENSG00000234519 [Sequence]  chr6:169067786-169069424 [Contig_View]  LOC102724357 [Vega]
ICGC DataPortalENSG00000234519
TCGA cBioPortalLOC102724357
AceView (NCBI)LOC102724357
Genatlas (Paris)LOC102724357
WikiGenes102724357
SOURCE (Princeton)LOC102724357
Genetics Home Reference (NIH)LOC102724357
Genomic and cartography
GoldenPath hg38 (UCSC)LOC102724357  -     chr6:169067786-169069424 +  6q27   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC102724357  -     6q27   [Description]    (hg19-Feb_2009)
EnsemblLOC102724357 - 6q27 [CytoView hg19]  LOC102724357 - 6q27 [CytoView hg38]
Mapping of homologs : NCBILOC102724357 [Mapview hg19]  LOC102724357 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA992013 BX096530
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC102724357
Cluster EST : UnigeneHs.129310 [ NCBI ]
CGAP (NCI)Hs.129310
Alternative Splicing GalleryENSG00000234519
Gene ExpressionLOC102724357 [ NCBI-GEO ]   LOC102724357 [ EBI - ARRAY_EXPRESS ]   LOC102724357 [ SEEK ]   LOC102724357 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC102724357 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102724357
GTEX Portal (Tissue expression)LOC102724357
Human Protein AtlasENSG00000234519-LOC102724357 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC102724357
DMDM Disease mutations102724357
Blocks (Seattle)LOC102724357
Human Protein Atlas [tissue]ENSG00000234519-LOC102724357 [tissue]
Protein Interaction databases
FunCoupENSG00000234519
BioGRIDLOC102724357
STRING (EMBL)LOC102724357
ZODIACLOC102724357
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease102724357
BioCentury BCIQLOC102724357
ClinGenLOC102724357
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102724357
Clinical trialLOC102724357
Miscellaneous
canSAR (ICR)LOC102724357 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC102724357
EVEXLOC102724357
GoPubMedLOC102724357
iHOPLOC102724357
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 Jul 30 14:05:28 CEST 2018

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