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LOC101928844 (uncharacterized LOC101928844)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928844
Atlas_Id 67442
Location 19p13.3  [Link to chromosome band 19p13]
Location_base_pair Starts at 5847467 and ends at 5858239 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)LOC101928844  101928844  uncharacterized LOC101928844
Aliases
GeneCards (Weizmann)LOC101928844
Ensembl hg19 (Hinxton)ENSG00000267709 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000267709 [Gene_View]  chr19:5847467-5858239 [Contig_View]  LOC101928844 [Vega]
ICGC DataPortalENSG00000267709
TCGA cBioPortalLOC101928844
AceView (NCBI)LOC101928844
Genatlas (Paris)LOC101928844
WikiGenes101928844
SOURCE (Princeton)LOC101928844
Genetics Home Reference (NIH)LOC101928844
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928844  -     chr19:5847467-5858239 +  19p13.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928844  -     19p13.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101928844 - 19p13.3 [CytoView hg19]  LOC101928844 - 19p13.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928844 [Mapview hg19]  LOC101928844 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC033124
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928844
Cluster EST : UnigeneHs.434577 [ NCBI ]
CGAP (NCI)Hs.434577
Alternative Splicing GalleryENSG00000267709
Gene ExpressionLOC101928844 [ NCBI-GEO ]   LOC101928844 [ EBI - ARRAY_EXPRESS ]   LOC101928844 [ SEEK ]   LOC101928844 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928844 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928844
GTEX Portal (Tissue expression)LOC101928844
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928844
DMDM Disease mutations101928844
Blocks (Seattle)LOC101928844
Human Protein AtlasENSG00000267709
Protein Interaction databases
FunCoupENSG00000267709
BioGRIDLOC101928844
STRING (EMBL)LOC101928844
ZODIACLOC101928844
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928844
BioCentury BCIQLOC101928844
ClinGenLOC101928844
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928844
Clinical trialLOC101928844
Miscellaneous
canSAR (ICR)LOC101928844 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928844
EVEXLOC101928844
GoPubMedLOC101928844
iHOPLOC101928844
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 : Wed Jun 7 16:05:46 CEST 2017

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