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LOC100507002 (uncharacterized LOC100507002)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100507002
Atlas_Id 66862
Location 17q24.1  [Link to chromosome band 17q24]
Location_base_pair Starts at 65100812 and ends at 65111094 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)LOC100507002  100507002  uncharacterized LOC100507002
Aliases
GeneCards (Weizmann)LOC100507002
Ensembl hg19 (Hinxton)ENSG00000263470 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263470 [Gene_View]  chr17:65100812-65111094 [Contig_View]  LOC100507002 [Vega]
ICGC DataPortalENSG00000263470
TCGA cBioPortalLOC100507002
AceView (NCBI)LOC100507002
Genatlas (Paris)LOC100507002
WikiGenes100507002
SOURCE (Princeton)LOC100507002
Genetics Home Reference (NIH)LOC100507002
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100507002  -     chr17:65100812-65111094 +  17q24.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100507002  -     17q24.1   [Description]    (hg19-Feb_2009)
EnsemblLOC100507002 - 17q24.1 [CytoView hg19]  LOC100507002 - 17q24.1 [CytoView hg38]
Mapping of homologs : NCBILOC100507002 [Mapview hg19]  LOC100507002 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DA745846
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100507002
Cluster EST : UnigeneHs.729924 [ NCBI ]
CGAP (NCI)Hs.729924
Alternative Splicing GalleryENSG00000263470
Gene ExpressionLOC100507002 [ NCBI-GEO ]   LOC100507002 [ EBI - ARRAY_EXPRESS ]   LOC100507002 [ SEEK ]   LOC100507002 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100507002 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507002
GTEX Portal (Tissue expression)LOC100507002
Human Protein AtlasENSG00000263470-LOC100507002 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100507002
DMDM Disease mutations100507002
Blocks (Seattle)LOC100507002
Human Protein Atlas [tissue]ENSG00000263470-LOC100507002 [tissue]
Protein Interaction databases
FunCoupENSG00000263470
BioGRIDLOC100507002
STRING (EMBL)LOC100507002
ZODIACLOC100507002
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100507002
BioCentury BCIQLOC100507002
ClinGenLOC100507002
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507002
Clinical trialLOC100507002
Miscellaneous
canSAR (ICR)LOC100507002 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100507002
EVEXLOC100507002
GoPubMedLOC100507002
iHOPLOC100507002
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 13:48:55 CET 2017

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