Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100506551 (uncharacterized LOC100506551)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506551
Atlas_Id 66831
Location 12q24.22  [Link to chromosome band 12q24]
Location_base_pair Starts at 116977440 and ends at 116987337 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)LOC100506551  100506551  uncharacterized LOC100506551
Aliases
GeneCards (Weizmann)LOC100506551
Ensembl hg19 (Hinxton)ENSG00000257279 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000257279 [Gene_View]  chr12:116977440-116987337 [Contig_View]  LOC100506551 [Vega]
ICGC DataPortalENSG00000257279
TCGA cBioPortalLOC100506551
AceView (NCBI)LOC100506551
Genatlas (Paris)LOC100506551
WikiGenes100506551
SOURCE (Princeton)LOC100506551
Genetics Home Reference (NIH)LOC100506551
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506551  -     chr12:116977440-116987337 -  12q24.22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506551  -     12q24.22   [Description]    (hg19-Feb_2009)
EnsemblLOC100506551 - 12q24.22 [CytoView hg19]  LOC100506551 - 12q24.22 [CytoView hg38]
Mapping of homologs : NCBINOS100506551 [Mapview hg19]  LOC100506551 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK127077 DB511872
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506551
Cluster EST : UnigeneHs.657861 [ NCBI ]
CGAP (NCI)Hs.657861
Alternative Splicing GalleryENSG00000257279
Gene ExpressionLOC100506551 [ NCBI-GEO ]   LOC100506551 [ EBI - ARRAY_EXPRESS ]   LOC100506551 [ SEEK ]   LOC100506551 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506551 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506551
GTEX Portal (Tissue expression)LOC100506551
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506551
DMDM Disease mutations100506551
Blocks (Seattle)LOC100506551
Human Protein AtlasENSG00000257279
Protein Interaction databases
FunCoupENSG00000257279
BioGRIDLOC100506551
STRING (EMBL)LOC100506551
ZODIACLOC100506551
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506551
BioCentury BCIQLOC100506551
ClinGenLOC100506551
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506551
Clinical trialLOC100506551
Miscellaneous
canSAR (ICR)LOC100506551 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506551
EVEXLOC100506551
GoPubMedLOC100506551
iHOPLOC100506551
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 13:18:56 CEST 2017

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