Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100294362 (uncharacterized LOC100294362)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100294362
Atlas_Id 66721
Location 17q25.3  [Link to chromosome band 17q25]
Location_base_pair Starts at 78325631 and ends at 78388968 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)LOC100294362  100294362  uncharacterized LOC100294362
Aliases
GeneCards (Weizmann)LOC100294362
Ensembl hg19 (Hinxton)ENSG00000263069 [Gene_View]  chr17:78325631-78388968 [Contig_View]  LOC100294362 [Vega]
Ensembl hg38 (Hinxton)ENSG00000263069 [Gene_View]  chr17:78325631-78388968 [Contig_View]  LOC100294362 [Vega]
ICGC DataPortalENSG00000263069
TCGA cBioPortalLOC100294362
AceView (NCBI)LOC100294362
Genatlas (Paris)LOC100294362
WikiGenes100294362
SOURCE (Princeton)LOC100294362
Genetics Home Reference (NIH)LOC100294362
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100294362  -     chr17:78325631-78388968 -  17q25.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100294362  -     17q25.3   [Description]    (hg38-Dec_2013)
EnsemblLOC100294362 - 17q25.3 [CytoView hg19]  LOC100294362 - 17q25.3 [CytoView hg38]
Mapping of homologs : NCBILOC100294362 [Mapview hg19]  LOC100294362 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF318359 AK125341 HG509523 HG509524 HG509525
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000017 NC_018928 NT_010783 NW_004929407
Consensus coding sequences : CCDS (NCBI)LOC100294362
Cluster EST : UnigeneHs.657519 [ NCBI ]
CGAP (NCI)Hs.657519
Alternative Splicing GalleryENSG00000263069
Gene ExpressionLOC100294362 [ NCBI-GEO ]   LOC100294362 [ EBI - ARRAY_EXPRESS ]   LOC100294362 [ SEEK ]   LOC100294362 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100294362 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100294362
GTEX Portal (Tissue expression)LOC100294362
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100294362
DMDM Disease mutations100294362
Blocks (Seattle)LOC100294362
Human Protein AtlasENSG00000263069
IPIIPI00445822   
Protein Interaction databases
FunCoupENSG00000263069
BioGRIDLOC100294362
STRING (EMBL)LOC100294362
ZODIACLOC100294362
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100294362
BioCentury BCIQLOC100294362
ClinGenLOC100294362
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100294362
Clinical trialLOC100294362
Miscellaneous
canSAR (ICR)LOC100294362 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100294362
EVEXLOC100294362
GoPubMedLOC100294362
iHOPLOC100294362
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 12:16:42 CET 2017

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