Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927322 (uncharacterized LOC101927322)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927322
Atlas_Id 67111
Location 18q21.32  [Link to chromosome band 18q21]
Location_base_pair Starts at 58670009 and ends at 58671873 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)LOC101927322  101927322  uncharacterized LOC101927322
Aliases
GeneCards (Weizmann)LOC101927322
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr18:58670009-58671873 [Contig_View]  LOC101927322 [Vega]
TCGA cBioPortalLOC101927322
AceView (NCBI)LOC101927322
Genatlas (Paris)LOC101927322
WikiGenes101927322
SOURCE (Princeton)LOC101927322
Genetics Home Reference (NIH)LOC101927322
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927322  -     chr18:58670009-58671873 -  18q21.32   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927322  -     18q21.32   [Description]    (hg19-Feb_2009)
EnsemblLOC101927322 - 18q21.32 [CytoView hg19]  LOC101927322 - 18q21.32 [CytoView hg38]
Mapping of homologs : NCBILOC101927322 [Mapview hg19]  LOC101927322 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA731738 BG723250 HY023467
RefSeq transcript (Entrez)NM_001289967
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927322
Cluster EST : UnigeneHs.644875 [ NCBI ]
CGAP (NCI)Hs.644875
Gene ExpressionLOC101927322 [ NCBI-GEO ]   LOC101927322 [ EBI - ARRAY_EXPRESS ]   LOC101927322 [ SEEK ]   LOC101927322 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927322 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927322
GTEX Portal (Tissue expression)LOC101927322
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927322
DMDM Disease mutations101927322
Blocks (Seattle)LOC101927322
Protein Interaction databases
BioGRIDLOC101927322
STRING (EMBL)LOC101927322
ZODIACLOC101927322
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927322
BioCentury BCIQLOC101927322
ClinGenLOC101927322
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927322
Clinical trialLOC101927322
Miscellaneous
canSAR (ICR)LOC101927322 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927322
EVEXLOC101927322
GoPubMedLOC101927322
iHOPLOC101927322
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 12:03:08 CET 2017

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