Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929551 (uncharacterized LOC101929551)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929551
Atlas_Id 67582
Location 2p25.1  [Link to chromosome band 2p25]
Location_base_pair Starts at 7886767 and ends at 7899655 bp from pter ( according to hg38-Dec_2013)

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)LOC101929551  101929551  uncharacterized LOC101929551
Aliases
GeneCards (Weizmann)LOC101929551
Ensembl hg19 (Hinxton)ENSG00000226506 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000226506 [Gene_View]  chr2:7886767-7899655 [Contig_View]  LOC101929551 [Vega]
ICGC DataPortalENSG00000226506
TCGA cBioPortalLOC101929551
AceView (NCBI)LOC101929551
Genatlas (Paris)LOC101929551
WikiGenes101929551
SOURCE (Princeton)LOC101929551
Genetics Home Reference (NIH)LOC101929551
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929551  -     chr2:7886767-7899655 -  2p25.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929551  -     2p25.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929551 - 2p25.1 [CytoView hg19]  LOC101929551 - 2p25.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929551 [Mapview hg19]  LOC101929551 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX093487
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929551
Cluster EST : UnigeneHs.116006 [ NCBI ]
CGAP (NCI)Hs.116006
Alternative Splicing GalleryENSG00000226506
Gene ExpressionLOC101929551 [ NCBI-GEO ]   LOC101929551 [ EBI - ARRAY_EXPRESS ]   LOC101929551 [ SEEK ]   LOC101929551 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929551 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929551
GTEX Portal (Tissue expression)LOC101929551
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929551
DMDM Disease mutations101929551
Blocks (Seattle)LOC101929551
Human Protein AtlasENSG00000226506
Protein Interaction databases
FunCoupENSG00000226506
BioGRIDLOC101929551
STRING (EMBL)LOC101929551
ZODIACLOC101929551
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929551
BioCentury BCIQLOC101929551
ClinGenLOC101929551
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929551
Clinical trialLOC101929551
Miscellaneous
canSAR (ICR)LOC101929551 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929551
EVEXLOC101929551
GoPubMedLOC101929551
iHOPLOC101929551
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Wed Jun 7 16:06:30 CEST 2017

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