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LOC101929007 (WAS/WASL-interacting protein family member 1)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929007
Atlas_Id 77145
Location 19p12  [Link to chromosome band 19p12]
Location_base_pair Starts at 21587432 and ends at 21594006 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
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)LOC101929007  101929007  WAS/WASL-interacting protein family member 1
Aliases
GeneCards (Weizmann)LOC101929007
Ensembl hg19 (Hinxton)ENSG00000268240 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000268240 [Gene_View]  chr19:21587432-21594006 [Contig_View]  LOC101929007 [Vega]
ICGC DataPortalENSG00000268240
TCGA cBioPortalLOC101929007
AceView (NCBI)LOC101929007
Genatlas (Paris)LOC101929007
WikiGenes101929007
SOURCE (Princeton)LOC101929007
Genetics Home Reference (NIH)LOC101929007
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929007  -     chr19:21587432-21594006 -  19p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929007  -     19p12   [Description]    (hg19-Feb_2009)
EnsemblLOC101929007 - 19p12 [CytoView hg19]  LOC101929007 - 19p12 [CytoView hg38]
Mapping of homologs : NCBILOC101929007 [Mapview hg19]  LOC101929007 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC033373
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929007
Cluster EST : UnigeneHs.515291 [ NCBI ]
CGAP (NCI)Hs.515291
Alternative Splicing GalleryENSG00000268240
Gene ExpressionLOC101929007 [ NCBI-GEO ]   LOC101929007 [ EBI - ARRAY_EXPRESS ]   LOC101929007 [ SEEK ]   LOC101929007 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929007 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929007
GTEX Portal (Tissue expression)LOC101929007
Human Protein AtlasENSG00000268240-LOC101929007 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929007
DMDM Disease mutations101929007
Blocks (Seattle)LOC101929007
Human Protein Atlas [tissue]ENSG00000268240-LOC101929007 [tissue]
Protein Interaction databases
FunCoupENSG00000268240
BioGRIDLOC101929007
STRING (EMBL)LOC101929007
ZODIACLOC101929007
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929007
BioCentury BCIQLOC101929007
ClinGenLOC101929007
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929007
Clinical trialLOC101929007
Miscellaneous
canSAR (ICR)LOC101929007 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929007
EVEXLOC101929007
GoPubMedLOC101929007
iHOPLOC101929007
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Nov 21 13:51:45 CET 2017

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