Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100507564 (uncharacterized LOC100507564)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100507564
Atlas_Id 66925
Location 1p32.3  [Link to chromosome band 1p32]
Location_base_pair Starts at 53704282 and ends at 53708455 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)LOC100507564  100507564  uncharacterized LOC100507564
Aliases
GeneCards (Weizmann)LOC100507564
Ensembl hg19 (Hinxton)ENSG00000226754 [Gene_View]  chr1:53704282-53708455 [Contig_View]  LOC100507564 [Vega]
Ensembl hg38 (Hinxton)ENSG00000226754 [Gene_View]  chr1:53704282-53708455 [Contig_View]  LOC100507564 [Vega]
ICGC DataPortalENSG00000226754
TCGA cBioPortalLOC100507564
AceView (NCBI)LOC100507564
Genatlas (Paris)LOC100507564
WikiGenes100507564
SOURCE (Princeton)LOC100507564
Genetics Home Reference (NIH)LOC100507564
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100507564  -     chr1:53704282-53708455 +  1p32.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100507564  -     1p32.3   [Description]    (hg38-Dec_2013)
EnsemblLOC100507564 - 1p32.3 [CytoView hg19]  LOC100507564 - 1p32.3 [CytoView hg38]
Mapping of homologs : NCBILOC100507564 [Mapview hg19]  LOC100507564 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC033363 HG492033
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000001 NC_018912 NT_032977 NW_004929290
Consensus coding sequences : CCDS (NCBI)LOC100507564
Cluster EST : UnigeneHs.592502 [ NCBI ]
CGAP (NCI)Hs.592502
Alternative Splicing GalleryENSG00000226754
Gene ExpressionLOC100507564 [ NCBI-GEO ]   LOC100507564 [ EBI - ARRAY_EXPRESS ]   LOC100507564 [ SEEK ]   LOC100507564 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100507564 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507564
GTEX Portal (Tissue expression)LOC100507564
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100507564
DMDM Disease mutations100507564
Blocks (Seattle)LOC100507564
Human Protein AtlasENSG00000226754
Protein Interaction databases
FunCoupENSG00000226754
BioGRIDLOC100507564
STRING (EMBL)LOC100507564
ZODIACLOC100507564
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100507564
BioCentury BCIQLOC100507564
ClinGenLOC100507564
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507564
Clinical trialLOC100507564
Miscellaneous
canSAR (ICR)LOC100507564 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100507564
EVEXLOC100507564
GoPubMedLOC100507564
iHOPLOC100507564
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 12:17:35 CET 2017

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