Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927523 (uncharacterized LOC101927523)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927523
Atlas_Id 67157
Location 10q25.1  [Link to chromosome band 10q25]
Location_base_pair Starts at 104474940 and ends at 104480275 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)LOC101927523  101927523  uncharacterized LOC101927523
Aliases
GeneCards (Weizmann)LOC101927523
Ensembl hg19 (Hinxton)ENSG00000225768 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000225768 [Gene_View]  chr10:104474940-104480275 [Contig_View]  LOC101927523 [Vega]
ICGC DataPortalENSG00000225768
TCGA cBioPortalLOC101927523
AceView (NCBI)LOC101927523
Genatlas (Paris)LOC101927523
WikiGenes101927523
SOURCE (Princeton)LOC101927523
Genetics Home Reference (NIH)LOC101927523
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927523  -     chr10:104474940-104480275 -  10q25.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927523  -     10q25.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101927523 - 10q25.1 [CytoView hg19]  LOC101927523 - 10q25.1 [CytoView hg38]
Mapping of homologs : NCBILOC101927523 [Mapview hg19]  LOC101927523 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC039476
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927523
Cluster EST : UnigeneHs.407539 [ NCBI ]
CGAP (NCI)Hs.407539
Alternative Splicing GalleryENSG00000225768
Gene ExpressionLOC101927523 [ NCBI-GEO ]   LOC101927523 [ EBI - ARRAY_EXPRESS ]   LOC101927523 [ SEEK ]   LOC101927523 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927523 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927523
GTEX Portal (Tissue expression)LOC101927523
Human Protein AtlasENSG00000225768-LOC101927523 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927523
DMDM Disease mutations101927523
Blocks (Seattle)LOC101927523
Human Protein Atlas [tissue]ENSG00000225768-LOC101927523 [tissue]
Protein Interaction databases
FunCoupENSG00000225768
BioGRIDLOC101927523
STRING (EMBL)LOC101927523
ZODIACLOC101927523
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927523
BioCentury BCIQLOC101927523
ClinGenLOC101927523
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927523
Clinical trialLOC101927523
Miscellaneous
canSAR (ICR)LOC101927523 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927523
EVEXLOC101927523
GoPubMedLOC101927523
iHOPLOC101927523
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 : Mon Nov 20 19:46:32 CET 2017

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