Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929073 (uncharacterized LOC101929073)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929073
Atlas_Id 67484
Location 10p12.1  [Link to chromosome band 10p12]
Location_base_pair Starts at 25924378 and ends at 25933710 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)LOC101929073  101929073  uncharacterized LOC101929073
Aliases
GeneCards (Weizmann)LOC101929073
Ensembl hg19 (Hinxton)ENSG00000226304 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000226304 [Gene_View]  chr10:25924378-25933710 [Contig_View]  LOC101929073 [Vega]
ICGC DataPortalENSG00000226304
TCGA cBioPortalLOC101929073
AceView (NCBI)LOC101929073
Genatlas (Paris)LOC101929073
WikiGenes101929073
SOURCE (Princeton)LOC101929073
Genetics Home Reference (NIH)LOC101929073
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929073  -     chr10:25924378-25933710 -  10p12.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929073  -     10p12.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929073 - 10p12.1 [CytoView hg19]  LOC101929073 - 10p12.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929073 [Mapview hg19]  LOC101929073 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI806694 AL137590
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929073
Cluster EST : UnigeneHs.734823 [ NCBI ]
CGAP (NCI)Hs.734823
Alternative Splicing GalleryENSG00000226304
Gene ExpressionLOC101929073 [ NCBI-GEO ]   LOC101929073 [ EBI - ARRAY_EXPRESS ]   LOC101929073 [ SEEK ]   LOC101929073 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929073 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929073
GTEX Portal (Tissue expression)LOC101929073
Human Protein AtlasENSG00000226304-LOC101929073 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929073
DMDM Disease mutations101929073
Blocks (Seattle)LOC101929073
Human Protein Atlas [tissue]ENSG00000226304-LOC101929073 [tissue]
Protein Interaction databases
FunCoupENSG00000226304
BioGRIDLOC101929073
STRING (EMBL)LOC101929073
ZODIACLOC101929073
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929073
BioCentury BCIQLOC101929073
ClinGenLOC101929073
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929073
Clinical trialLOC101929073
Miscellaneous
canSAR (ICR)LOC101929073 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929073
EVEXLOC101929073
GoPubMedLOC101929073
iHOPLOC101929073
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 : Mon Nov 20 19:48:13 CET 2017

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