Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929172 (uncharacterized LOC101929172)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929172
Atlas_Id 67507
Location 8p21.3  [Link to chromosome band 8p21]
Location_base_pair Starts at 21298239 and ends at 21309449 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)LOC101929172  101929172  uncharacterized LOC101929172
Aliases
GeneCards (Weizmann)LOC101929172
Ensembl hg19 (Hinxton)ENSG00000254334 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000254334 [Gene_View]  chr8:21298239-21309449 [Contig_View]  LOC101929172 [Vega]
ICGC DataPortalENSG00000254334
TCGA cBioPortalLOC101929172
AceView (NCBI)LOC101929172
Genatlas (Paris)LOC101929172
WikiGenes101929172
SOURCE (Princeton)LOC101929172
Genetics Home Reference (NIH)LOC101929172
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929172  -     chr8:21298239-21309449 +  8p21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929172  -     8p21.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101929172 - 8p21.3 [CytoView hg19]  LOC101929172 - 8p21.3 [CytoView hg38]
Mapping of homologs : NCBILOC101929172 [Mapview hg19]  LOC101929172 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK057515
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929172
Cluster EST : UnigeneHs.128668 [ NCBI ]
CGAP (NCI)Hs.128668
Alternative Splicing GalleryENSG00000254334
Gene ExpressionLOC101929172 [ NCBI-GEO ]   LOC101929172 [ EBI - ARRAY_EXPRESS ]   LOC101929172 [ SEEK ]   LOC101929172 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929172 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929172
GTEX Portal (Tissue expression)LOC101929172
Human Protein AtlasENSG00000254334-LOC101929172 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929172
DMDM Disease mutations101929172
Blocks (Seattle)LOC101929172
Human Protein Atlas [tissue]ENSG00000254334-LOC101929172 [tissue]
Protein Interaction databases
FunCoupENSG00000254334
BioGRIDLOC101929172
STRING (EMBL)LOC101929172
ZODIACLOC101929172
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929172
BioCentury BCIQLOC101929172
ClinGenLOC101929172
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929172
Clinical trialLOC101929172
Miscellaneous
canSAR (ICR)LOC101929172 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929172
EVEXLOC101929172
GoPubMedLOC101929172
iHOPLOC101929172
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 : Thu Nov 9 12:05:05 CET 2017

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