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LOC101559451 (uncharacterized LOC101559451)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101559451
Atlas_Id 67001
Location 17p13.2  [Link to chromosome band 17p13]
Location_base_pair Starts at 4704230 and ends at 4705529 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)LOC101559451  101559451  uncharacterized LOC101559451
Aliases
GeneCards (Weizmann)LOC101559451
Ensembl hg19 (Hinxton)ENSG00000244184 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000244184 [Gene_View]  chr17:4704230-4705529 [Contig_View]  LOC101559451 [Vega]
ICGC DataPortalENSG00000244184
TCGA cBioPortalLOC101559451
AceView (NCBI)LOC101559451
Genatlas (Paris)LOC101559451
WikiGenes101559451
SOURCE (Princeton)LOC101559451
Genetics Home Reference (NIH)LOC101559451
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101559451  -     chr17:4704230-4705529 +  17p13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101559451  -     17p13.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101559451 - 17p13.2 [CytoView hg19]  LOC101559451 - 17p13.2 [CytoView hg38]
/åxtdef.html#MAPVIEW TARGET=NCBI>Mapping of homologs : NCBILOC101559451 [Mapview hg19]  LOC101559451 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX109211
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101559451
Cluster EST : UnigeneHs.634966 [ NCBI ]
CGAP (NCI)Hs.634966
Alternative Splicing GalleryENSG00000244184
Gene ExpressionLOC101559451 [ NCBI-GEO ]   LOC101559451 [ EBI - ARRAY_EXPRESS ]   LOC101559451 [ SEEK ]   LOC101559451 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101559451 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101559451
GTEX Portal (Tissue expression)LOC101559451
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101559451
DMDM Disease mutations101559451
Blocks (Seattle)LOC101559451
Human Protein AtlasENSG00000244184
Protein Interaction databases
FunCoupENSG00000244184
BioGRIDLOC101559451
STRING (EMBL)LOC101559451
ZODIACLOC101559451
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101559451
BioCentury BCIQLOC101559451
ClinGenLOC101559451
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101559451
Clinical trialLOC101559451
Miscellaneous
canSAR (ICR)LOC101559451 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101559451
EVEXLOC101559451
GoPubMedLOC101559451
iHOPLOC101559451
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 13:19:30 CEST 2017

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