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LOC100507663 (uncharacterized LOC100507663)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100507663
Atlas_Id 66935
Location 10p11.22  [Link to chromosome band 10p11]
Location_base_pair Starts at 31310004 and ends at 31311752 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100507663  100507663  uncharacterized LOC100507663
Aliases
GeneCards (Weizmann)LOC100507663
Ensembl hg19 (Hinxton) [Gene_View]  chr10:31310004-31311752 [Contig_View]  LOC100507663 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr10:31310004-31311752 [Contig_View]  LOC100507663 [Vega]
TCGA cBioPortalLOC100507663
AceView (NCBI)LOC100507663
Genatlas (Paris)LOC100507663
WikiGenes100507663
SOURCE (Princeton)LOC100507663
Genetics Home Reference (NIH)LOC100507663
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100507663  -     chr10:31310004-31311752 -  10p11.22   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100507663  -     10p11.22   [Description]    (hg38-Dec_2013)
EnsemblLOC100507663 - 10p11.22 [CytoView hg19]  LOC100507663 - 10p11.22 [CytoView hg38]
Mapping of homologs : NCBILOC100507663 [Mapview hg19]  LOC100507663 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK129895
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)AC_000142 NC_000010 NC_018921 NT_008705 NW_001837932 NW_004078062
Consensus coding sequences : CCDS (NCBI)LOC100507663
Cluster EST : UnigeneHs.663402 [ NCBI ]
CGAP (NCI)Hs.663402
Gene ExpressionLOC100507663 [ NCBI-GEO ]   LOC100507663 [ EBI - ARRAY_EXPRESS ]   LOC100507663 [ SEEK ]   LOC100507663 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100507663 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507663
GTEX Portal (Tissue expression)LOC100507663
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100507663
DMDM Disease mutations100507663
Blocks (Seattle)LOC100507663
IPIIPI00442893   
Protein Interaction databases
BioGRIDLOC100507663
STRING (EMBL)LOC100507663
ZODIACLOC100507663
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100507663
BioCentury BCIQLOC100507663
ClinGenLOC100507663
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507663
Clinical trialLOC100507663
Miscellaneous
canSAR (ICR)LOC100507663 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100507663
EVEXLOC100507663
GoPubMedLOC100507663
iHOPLOC100507663
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 12:17:38 CET 2017

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