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LOC100506639 (uncharacterized LOC100506639)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506639
Atlas_Id 66836
Location 5p12  [Link to chromosome band 5p12]
Location_base_pair Starts at 43067125 and ends at 43093660 bp from pter ( according to hg19-Feb_2009)

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)LOC100506639  100506639  uncharacterized LOC100506639
Aliases
GeneCards (Weizmann)LOC100506639
Ensembl hg19 (Hinxton) [Gene_View]  chr5:43067125-43093660 [Contig_View]  LOC100506639 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr5:43067125-43093660 [Contig_View]  LOC100506639 [Vega]
TCGA cBioPortalLOC100506639
AceView (NCBI)LOC100506639
Genatlas (Paris)LOC100506639
WikiGenes100506639
SOURCE (Princeton)LOC100506639
Genetics Home Reference (NIH)LOC100506639
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100506639  -     chr5:43067125-43093660 +  5p12   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100506639  -     5p12   [Description]    (hg38-Dec_2013)
EnsemblLOC100506639 - 5p12 [CytoView hg19]  LOC100506639 - 5p12 [CytoView hg38]
Mapping of homologs : NCBILOC100506639 [Mapview hg19]  LOC100506639 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF131822 AK311398 BE545768 BG000146 CN309143
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000005 NC_018916 NT_006576 NW_004929321
Consensus coding sequences : CCDS (NCBI)LOC100506639
Cluster EST : UnigeneHs.666493 [ NCBI ]
CGAP (NCI)Hs.666493
Gene ExpressionLOC100506639 [ NCBI-GEO ]   LOC100506639 [ EBI - ARRAY_EXPRESS ]   LOC100506639 [ SEEK ]   LOC100506639 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506639 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506639
GTEX Portal (Tissue expression)LOC100506639
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506639
DMDM Disease mutations100506639
Blocks (Seattle)LOC100506639
Protein Interaction databases
BioGRIDLOC100506639
STRING (EMBL)LOC100506639
ZODIACLOC100506639
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506639
BioCentury BCIQLOC100506639
ClinGenLOC100506639
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506639
Clinical trialLOC100506639
Miscellaneous
canSAR (ICR)LOC100506639 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506639
EVEXLOC100506639
GoPubMedLOC100506639
iHOPLOC100506639
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 Mar 14 12:17:13 CET 2017

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