Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929054 (uncharacterized LOC101929054)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929054
Atlas_Id 77444
Location 3p21.2  [Link to chromosome band 3p21]
Location_base_pair Starts at 52239238 and ends at 52241097 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 t(is gEne- go to  How to contribute

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC101929054  101929054  uncharacterized LOC101929054
Aliases
GeneCards (Weizmann)LOC101929054
Ensembl hg19 (Hinxton)ENSG00000243224 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000243224 [Gene_View]  chr3:52239238-52241097 [Contig_View]  LOC101929054 [Vega]
ICGC DataPortalENSG00000243224
TCGA cBioPortalLOC101929054
AceView (NCBI)LOC101929054
Genatlas (Paris)LOC101929054
WikiGenes101929054
SOURCE (Princeton)LOC101929054
Genetics Home Reference (NIH)LOC101929054
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929054  -     chr3:52239238-52241097 +  3p21.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929054  -     3p21.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101929054 - 3p21.2 [CytoView hg19]  LOC101929054 - 3p21.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929054 [Mapview hg19]  LOC101929054 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC039681 HY101534
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929054
Cluster EST : UnigeneHs.281931 [ NCBI ]
CGAP (NCI)Hs.281931
Alternative Splicing GalleryENSG00000243224
Gene ExpressionLOC101929054 [ NCBI-GEO ]   LOC101929054 [ EBI - ARRAY_EXPRESS ]   LOC101929054 [ SEEK ]   LOC101929054 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929054 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929054
GTEX Portal (Tissue expression)LOC101929054
Human Protein AtlasENSG00000243224-LOC101929054 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929054
DMDM Disease mutations101929054
Blocks (Seattle)LOC101929054
Human Protein Atlas [tissue]ENSG00000243224-LOC101929054 [tissue]
Protein Interaction databases
FunCoupENSG00000243224
BioGRIDLOC101929054
STRING (EMBL)LOC101929054
ZODIACLOC101929054
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929054
BioCentury BCIQLOC101929054
ClinGenLOC101929054
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929054
Clinical trialLOC101929054
Miscellaneous
canSAR (ICR)LOC101929054 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929054
EVEXLOC101929054
GoPubMedLOC101929054
iHOPLOC101929054
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 : Tue Nov 21 13:51:47 CET 2017

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