Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100131655 (uncharacterized LOC100131655)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100131655
Atlas_Id 66501
Location 18q23  [Link to chromosome band 18q23]
Location_base_pair Starts at 76794732 and ends at 76822295 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)LOC100131655  100131655  uncharacterized LOC100131655
Aliases
GeneCards (Weizmann)LOC100131655
Ensembl hg19 (Hinxton)ENSG00000264278 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000264278 [Gene_View]  chr18:76794732-76822295 [Contig_View]  LOC100131655 [Vega]
ICGC DataPortalENSG00000264278
TCGA cBioPortalLOC100131655
AceView (NCBI)LOC100131655
Genatlas (Paris)LOC100131655
WikiGenes100131655
SOURCE (Princeton)LOC100131655
Genetics Home Reference (NIH)LOC100131655
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100131655  -     chr18:76794732-76822295 -  18q23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100131655  -     18q23   [Description]    (hg19-Feb_2009)
EnsemblLOC100131655 - 18q23 [CytoView hg19]  LOC100131655 - 18q23 [CytoView hg38]
Mapping of homologs : NCBILOC100131655 [Mapview hg19]  LOC100131655 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC032908
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100131655
Cluster EST : UnigeneHs.385806 [ NCBI ]
CGAP (NCI)Hs.385806
Alternative Splicing GalleryENSG00000264278
Gene ExpressionLOC100131655 [ NCBI-GEO ]   LOC100131655 [ EBI - ARRAY_EXPRESS ]   LOC100131655 [ SEEK ]   LOC100131655 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100131655 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100131655
GTEX Portal (Tissue expression)LOC100131655
Human Protein AtlasENSG00000264278-LOC100131655 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100131655
DMDM Disease mutations100131655
Blocks (Seattle)LOC100131655
Human Protein Atlas [tissue]ENSG00000264278-LOC100131655 [tissue]
Protein Interaction databases
FunCoupENSG00000264278
BioGRIDLOC100131655
STRING (EMBL)LOC100131655
ZODIACLOC100131655
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100131655
BioCentury BCIQLOC100131655
ClinGenLOC100131655
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100131655
Clinical trialLOC100131655
Miscellaneous
canSAR (ICR)LOC100131655 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100131655
EVEXLOC100131655
GoPubMedLOC100131655
iHOPLOC100131655
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 12:00:43 CET 2017

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