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LOC101929902 (uncharacterized LOC101929902)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929902
Atlas_Id 77022
Location 1q42.2  [Link to chromosome band 1q42]
Location_base_pair Starts at 232311492 and ends at 232313111 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)LOC101929902  101929902  uncharacterized LOC101929902
Aliases
GeneCards (Weizmann)LOC101929902
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr1:232311492-232313111 [Contig_View]  LOC101929902 [Vega]
TCGA cBioPortalLOC101929902
AceView (NCBI)LOC101929902
Genatlas (Paris)LOC101929902
WikiGenes101929902
SOURCE (Princeton)LOC101929902
Genetics Home Reference (NIH)LOC101929902
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929902  -     chr1:232311492-232313111 -  1q42.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929902  -     1q42.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101929902 - 1q42.2 [CytoView hg19]  LOC101929902 - 1q42.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929902 [Mapview hg19]  LOC101929902 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC038418
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929902
Cluster EST : UnigeneHs.385722 [ NCBI ]
CGAP (NCI)Hs.385722
Gene ExpressionLOC101929902 [ NCBI-GEO ]   LOC101929902 [ EBI - ARRAY_EXPRESS ]   LOC101929902 [ SEEK ]   LOC101929902 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929902 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929902
GTEX Portal (Tissue expression)LOC101929902
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929902
DMDM Disease mutations101929902
Blocks (Seattle)LOC101929902
Protein Interaction databases
BioGRIDLOC101929902
STRING (EMBL)LOC101929902
ZODIACLOC101929902
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929902
BioCentury BCIQLOC101929902
ClinGenLOC101929902
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929902
Clinical trialLOC101929902
Miscellaneous
canSAR (ICR)LOC101929902 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929902
EVEXLOC101929902
GoPubMedLOC101929902
iHOPLOC101929902
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 19:48:56 CET 2017

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