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LOC101929770 (uncharacterized LOC101929770)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929770
Atlas_Id 77662
Location 6p21.1  [Link to chromosome band 6p21]
Location_base_pair Starts at 44731118 and ends at 44737356 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC101929770  101929770  uncharacterized LOC101929770
Aliases
GeneCards (Weizmann)LOC101929770
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr6:44731118-44737356 [Contig_View]  LOC101929770 [Vega]
TCGA cBioPortalLOC101929770
AceView (NCBI)LOC101929770
Genatlas (Paris)LOC101929770
WikiGenes101929770
SOURCE (Princeton)LOC101929770
Genetics Home Reference (NIH)LOC101929770
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929770  -     chr6:44731118-44737356 +  6p21.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929770  -     6p21.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929770 - 6p21.1 [CytoView hg19]  LOC101929770 - 6p21.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929770 [Mapview hg19]  LOC101929770 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX647715
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929770
Cluster EST : UnigeneHs.628573 [ NCBI ]
CGAP (NCI)Hs.628573
Gene ExpressionLOC101929770 [ NCBI-GEO ]   LOC101929770 [ EBI - ARRAY_EXPRESS ]   LOC101929770 [ SEEK ]   LOC101929770 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929770 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929770
GTEX Portal (Tissue expression)LOC101929770
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929770
DMDM Disease mutations101929770
Blocks (Seattle)LOC101929770
Protein Interaction databases
BioGRIDLOC101929770
STRING (EMBL)LOC101929770
ZODIACLOC101929770
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929770
BioCentury BCIQLOC101929770
ClinGenLOC101929770
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929770
Clinical trialLOC101929770
Miscellaneous
canSAR (ICR)LOC101929770 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929770
EVEXLOC101929770
GoPubMedLOC101929770
iHOPLOC101929770
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 Jul 30 14:04:49 CEST 2018

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