Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101805491 (uncharacterized LOC101805491)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101805491
Atlas_Id 67003
Location 2p21  [Link to chromosome band 2p21]
Location_base_pair Starts at 46429190 and ends at 46441833 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)LOC101805491  101805491  uncharacterized LOC101805491
Aliases
GeneCards (Weizmann)LOC101805491
Ensembl hg19 (Hinxton)ENSG00000187600 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000187600 [Gene_View]  chr2:46429190-46441833 [Contig_View]  LOC101805491 [Vega]
ICGC DataPortalENSG00000187600
TCGA cBioPortalLOC101805491
AceView (NCBI)LOC101805491
Genatlas (Paris)LOC101805491
WikiGenes101805491
SOURCE (Princeton)LOC101805491
Genetics Home Reference (NIH)LOC101805491
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101805491  -     chr2:46429190-46441833 +  2p21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101805491  -     2p21   [Description]    (hg19-Feb_2009)
EnsemblLOC101805491 - 2p21 [CytoView hg19]  LOC101805491 - 2p21 [CytoView hg38]
Mapping of homologs : NCBILOC101805491 [Mapview hg19]  LOC101805491 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC031304 BG181886 BI461479
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101805491
Cluster EST : UnigeneHs.304781 [ NCBI ]
CGAP (NCI)Hs.304781
Alternative Splicing GalleryENSG00000187600
Gene ExpressionLOC101805491 [ NCBI-GEO ]   LOC101805491 [ EBI - ARRAY_EXPRESS ]   LOC101805491 [ SEEK ]   LOC101805491 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101805491 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101805491
GTEX Portal (Tissue expression)LOC101805491
Human Protein AtlasENSG00000187600-LOC101805491 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101805491
DMDM Disease mutations101805491
Blocks (Seattle)LOC101805491
Human Protein Atlas [tissue]ENSG00000187600-LOC101805491 [tissue]
Protein Interaction databases
FunCoupENSG00000187600
BioGRIDLOC101805491
STRING (EMBL)LOC101805491
ZODIACLOC101805491
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101805491
BioCentury BCIQLOC101805491
ClinGenLOC101805491
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101805491
Clinical trialLOC101805491
Miscellaneous
canSAR (ICR)LOC101805491 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101805491
EVEXLOC101805491
GoPubMedLOC101805491
iHOPLOC101805491
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 19:45:51 CET 2017

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