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LOC102723895 (uncharacterized LOC102723895)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 102723895
Atlas_Id 67711
Location 11q22.3  [Link to chromosome band 11q22]
Location_base_pair Starts at 104568489 and ends at 104609302 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC102723895  102723895  uncharacterized LOC102723895
Aliases
GeneCards (Weizmann)LOC102723895
Ensembl hg19 (Hinxton)ENSG00000256422 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000256422 [Gene_View]  chr11:104568489-104609302 [Contig_View]  LOC102723895 [Vega]
ICGC DataPortalENSG00000256422
TCGA cBioPortalLOC102723895
AceView (NCBI)LOC102723895
Genatlas (Paris)LOC102723895
WikiGenes102723895
SOURCE (Princeton)LOC102723895
Genetics Home Reference (NIH)LOC102723895
Genomic and cartography
GoldenPath hg38 (UCSC)LOC102723895  -     chr11:104568489-104609302 -  11q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC102723895  -     11q22.3   [Description]    (hg19-Feb_2009)
EnsemblLOC102723895 - 11q22.3 [CytoView hg19]  LOC102723895 - 11q22.3 [CytoView hg38]
Mapping of homologs : NCBILOC102723895 [Mapview hg19]  LOC102723895 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DA109127 N63497
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC102723895
Cluster EST : UnigeneHs.48803 [ NCBI ]
CGAP (NCI)Hs.48803
Alternative Splicing GalleryENSG00000256422
Gene ExpressionLOC102723895 [ NCBI-GEO ]   LOC102723895 [ EBI - ARRAY_EXPRESS ]   LOC102723895 [ SEEK ]   LOC102723895 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC102723895 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102723895
GTEX Portal (Tissue expression)LOC102723895
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC102723895
DMDM Disease mutations102723895
Blocks (Seattle)LOC102723895
Human Protein AtlasENSG00000256422
Protein Interaction databases
FunCoupENSG00000256422
BioGRIDLOC102723895
STRING (EMBL)LOC102723895
ZODIACLOC102723895
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease102723895
BioCentury BCIQLOC102723895
ClinGenLOC102723895
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102723895
Clinical trialLOC102723895
Miscellaneous
canSAR (ICR)LOC102723895 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC102723895
EVEXLOC102723895
GoPubMedLOC102723895
iHOPLOC102723895
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed May 31 15:18:20 CEST 2017

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