Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

LOC101927588 (uncharacterized LOC101927588)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927588
Atlas_Id 67173
Location 8q24.13  [Link to chromosome band 8q24]
Location_base_pair Starts at 124192691 and ends at 124247398 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)LOC101927588  101927588  uncharacterized LOC101927588
Aliases
GeneCards (Weizmann)LOC101927588
Ensembl hg19 (Hinxton)ENSG00000214803 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000214803 [Gene_View]  chr8:124192691-124247398 [Contig_View]  LOC101927588 [Vega]
ICGC DataPortalENSG00000214803
TCGA cBioPortalLOC101927588
AceView (NCBI)LOC101927588
Genatlas (Paris)LOC101927588
WikiGenes101927588
SOURCE (Princeton)LOC101927588
Genetics Home Reference (NIH)LOC101927588
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927588  -     chr8:124192691-124247398 -  8q24.13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927588  -     8q24.13   [Description]    (hg19-Feb_2009)
EnsemblLOC101927588 - 8q24.13 [CytoView hg19]  LOC101927588 - 8q24.13 [CytoView hg38]
Mapping of homologs : NCBILOC101927588 [Mapview hg19]  LOC101927588 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC015129
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927588
Cluster EST : UnigeneHs.617072 [ NCBI ]
CGAP (NCI)Hs.617072
Alternative Splicing GalleryENSG00000214803
Gene ExpressionLOC101927588 [ NCBI-GEO ]   LOC101927588 [ EBI - ARRAY_EXPRESS ]   LOC101927588 [ SEEK ]   LOC101927588 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927588 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927588
GTEX Portal (Tissue expression)LOC101927588
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927588
DMDM Disease mutations101927588
Blocks (Seattle)LOC101927588
Human Protein AtlasENSG00000214803
Protein Interaction databases
FunCoupENSG00000214803
BioGRIDLOC101927588
STRING (EMBL)LOC101927588
ZODIACLOC101927588
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927588
BioCentury BCIQLOC101927588
ClinGenLOC101927588
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927588
Clinical trialLOC101927588
Miscellaneous
canSAR (ICR)LOC101927588 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927588
EVEXLOC101927588
GoPubMedLOC101927588
iHOPLOC101927588
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 : Mon Sep 18 13:20:09 CEST 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.