Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100505851 (uncharacterized LOC100505851)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100505851
Atlas_Id 66759
Location 19p12  [Link to chromosome band 19p12]
Location_base_pair Starts at 23919081 and ends at 23957930 bp from pter ( according to hg38-Dec_2013)
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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100505851  100505851  uncharacterized LOC100505851
Aliases
GeneCards (Weizmann)LOC100505851
Ensembl hg19 (Hinxton)ENSG00000269289 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000269289 [Gene_View]  chr19:23919081-23957930 [Contig_View]  LOC100505851 [Vega]
ICGC DataPortalENSG00000269289
TCGA cBioPortalLOC100505851
AceView (NCBI)LOC100505851
Genatlas (Paris)LOC100505851
WikiGenes100505851
SOURCE (Princeton)LOC100505851
Genetics Home Reference (NIH)LOC100505851
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100505851  -     chr19:23919081-23957930 -  19p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100505851  -     19p12   [Description]    (hg19-Feb_2009)
EnsemblLOC100505851 - 19p12 [CytoView hg19]  LOC100505851 - 19p12 [CytoView hg38]
Mapping of homologs : NCBILOC100505851 [Mapview hg19]  LOC100505851 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK125686 BC015383
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100505851
Cluster EST : UnigeneHs.190888 [ NCBI ]
CGAP (NCI)Hs.190888
Alternative Splicing GalleryENSG00000269289
Gene ExpressionLOC100505851 [ NCBI-GEO ]   LOC100505851 [ EBI - ARRAY_EXPRESS ]   LOC100505851 [ SEEK ]   LOC100505851 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100505851 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505851
GTEX Portal (Tissue expression)LOC100505851
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100505851
DMDM Disease mutations100505851
Blocks (Seattle)LOC100505851
Human Protein AtlasENSG00000269289
Protein Interaction databases
FunCoupENSG00000269289
BioGRIDLOC100505851
STRING (EMBL)LOC100505851
ZODIACLOC100505851
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100505851
BioCentury BCIQLOC100505851
ClinGenLOC100505851
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505851
Clinical trialLOC100505851
Miscellaneous
canSAR (ICR)LOC100505851 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100505851
EVEXLOC100505851
GoPubMedLOC100505851
iHOPLOC100505851
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 : Wed Jun 7 16:02:24 CEST 2017

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