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LOC102724908 (uncharacterized LOC102724908)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 102724908
Atlas_Id 78458
Location 19q12  [Link to chromosome band 19q12]
Location_base_pair Starts at 28606688 and ends at 28615229 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)LOC102724908  102724908  uncharacterized LOC102724908
Aliases
GeneCards (Weizmann)LOC102724908
Ensembl hg19 (Hinxton)ENSG00000266976 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266976 [Gene_View]  chr19:28606688-28615229 [Contig_View]  LOC102724908 [Vega]
ICGC DataPortalENSG00000266976
TCGA cBioPortalLOC102724908
AceView (NCBI)LOC102724908
Genatlas (Paris)LOC102724908
WikiGenes102724908
SOURCE (Princeton)LOC102724908
Genetics Home Reference (NIH)LOC102724908
Genomic and cartography
GoldenPath hg38 (UCSC)LOC102724908  -     chr19:28606688-28615229 +  19q12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC102724908  -     19q12   [Description]    (hg19-Feb_2009)
EnsemblLOC102724908 - 19q12 [CytoView hg19]  LOC102724908 - 19q12 [CytoView hg38]
Mapping of homologs : NCBILOC102724908 [Mapview hg19]  LOC102724908 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC102724908
Alternative Splicing GalleryENSG00000266976
Gene ExpressionLOC102724908 [ NCBI-GEO ]   LOC102724908 [ EBI - ARRAY_EXPRESS ]   LOC102724908 [ SEEK ]   LOC102724908 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC102724908 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102724908
GTEX Portal (Tissue expression)LOC102724908
Human Protein AtlasENSG00000266976-LOC102724908 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC102724908
DMDM Disease mutations102724908
Blocks (Seattle)LOC102724908
Human Protein Atlas [tissue]ENSG00000266976-LOC102724908 [tissue]
Protein Interaction databases
FunCoupENSG00000266976
BioGRIDLOC102724908
STRING (EMBL)LOC102724908
ZODIACLOC102724908
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease102724908
BioCentury BCIQLOC102724908
ClinGenLOC102724908
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102724908
Clinical trialLOC102724908
Miscellaneous
canSAR (ICR)LOC102724908 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC102724908
EVEXLOC102724908
GoPubMedLOC102724908
iHOPLOC102724908
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 : Thu Nov 9 12:06:25 CET 2017

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