Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927391 (uncharacterized LOC101927391)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927391
Atlas_Id 67124
Location 7p21.3  [Link to chromosome band 7p21]
Location_base_pair Starts at 7550104 and ends at 7566065 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)LOC101927391  101927391  uncharacterized LOC101927391
Aliases
GeneCards (Weizmann)LOC101927391
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr7:7550104-7566065 [Contig_View]  LOC101927391 [Vega]
TCGA cBioPortalLOC101927391
AceView (NCBI)LOC101927391
Genatlas (Paris)LOC101927391
WikiGenes101927391
SOURCE (Princeton)LOC101927391
Genetics Home Reference (NIH)LOC101927391
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927391  -     chr7:7550104-7566065 -  7p21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927391  -     7p21.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101927391 - 7p21.3 [CytoView hg19]  LOC101927391 - 7p21.3 [CytoView hg38]
Mapping of homologs : NCBILOC101927391 [Mapview hg19]  LOC101927391 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BQ370223 BU607350 BX091963 DA832074
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927391
Cluster EST : UnigeneHs.738913 [ NCBI ]
CGAP (NCI)Hs.738913
Gene ExpressionLOC101927391 [ NCBI-GEO ]   LOC101927391 [ EBI - ARRAY_EXPRESS ]   LOC101927391 [ SEEK ]   LOC101927391 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927391 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927391
GTEX Portal (Tissue expression)LOC101927391
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927391
DMDM Disease mutations101927391
Blocks (Seattle)LOC101927391
Protein Interaction databases
BioGRIDLOC101927391
STRING (EMBL)LOC101927391
ZODIACLOC101927391
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927391
BioCentury BCIQLOC101927391
ClinGenLOC101927391
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927391
Clinical trialLOC101927391
Miscellaneous
canSAR (ICR)LOC101927391 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927391
EVEXLOC101927391
GoPubMedLOC101927391
iHOPLOC101927391
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 19:46:23 CET 2017

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