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LOC100505727 (uncharacterized LOC100505727)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100505727
Atlas_Id 77408
Location 21q22.3  [Link to chromosome band 21q22]
Location_base_pair Starts at 44485571 and ends at 44491139 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100505727  100505727  uncharacterized LOC100505727
Aliases
GeneCards (Weizmann)LOC100505727
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr21:44485571-44491139 [Contig_View]  LOC100505727 [Vega]
TCGA cBioPortalLOC100505727
AceView (NCBI)LOC100505727
Genatlas (Paris)LOC100505727
WikiGenes100505727
SOURCE (Princeton)LOC100505727
Genetics Home Reference (NIH)LOC100505727
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100505727  -     chr21:44485571-44491139 +  21q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100505727  -     21q22.3   [Description]    (hg19-Feb_2009)
EnsemblLOC100505727 - 21q22.3 [CytoView hg19]  LOC100505727 - 21q22.3 [CytoView hg38]
Mapping of homologs : NCBILOC100505727 [Mapview hg19]  LOC100505727 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK057525
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100505727
Cluster EST : UnigeneHs.572852 [ NCBI ]
CGAP (NCI)Hs.572852
Gene ExpressionLOC100505727 [ NCBI-GEO ]   LOC100505727 [ EBI - ARRAY_EXPRESS ]   LOC100505727 [ SEEK ]   LOC100505727 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100505727 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505727
GTEX Portal (Tissue expression)LOC100505727
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100505727
DMDM Disease mutations100505727
Blocks (Seattle)LOC100505727
Protein Interaction databases
BioGRIDLOC100505727
STRING (EMBL)LOC100505727
ZODIACLOC100505727
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100505727
BioCentury BCIQLOC100505727
ClinGenLOC100505727
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505727
Clinical trialLOC100505727
Miscellaneous
canSAR (ICR)LOC100505727 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100505727
EVEXLOC100505727
GoPubMedLOC100505727
iHOPLOC100505727
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 12:01:41 CET 2017

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