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HRASLS (-)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 57110
Atlas_Id 40863
Location -  [Link to chromosome band ]
Location_base_pair Starts at 193241128 and ends at 193270855 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)HRASLS  57110  -
Aliases
GeneCards (Weizmann)HRASLS
Ensembl hg19 (Hinxton)ENSG00000127252 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000127252 [Gene_View]  ENSG00000127252 [Sequence]  chr3:193241128-193270855 [Contig_View]  HRASLS [Vega]
ICGC DataPortalENSG00000127252
TCGA cBioPortalHRASLS
AceView (NCBI)HRASLS
Genatlas (Paris)HRASLS
WikiGenes57110
SOURCE (Princeton)HRASLS
Genetics Home Reference (NIH)HRASLS
Genomic and cartography
GoldenPath hg38 (UCSC)HRASLS  -     chr3:193241128-193270855 +  -   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)HRASLS  -     -   [Description]    (hg19-Feb_2009)
GoldenPathHRASLS - - [CytoView hg19]  HRASLS - - [CytoView hg38]
ImmunoBaseENSG00000127252
Mapping of homologs : NCBIHRASLS [Mapview hg19]  HRASLS [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)HRASLS
Alternative Splicing GalleryENSG00000127252
Gene ExpressionHRASLS [ NCBI-GEO ]   HRASLS [ EBI - ARRAY_EXPRESS ]   HRASLS [ SEEK ]   HRASLS [ MEM ]
Gene Expression Viewer (FireBrowse)HRASLS [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)57110
GTEX Portal (Tissue expression)HRASLS
Human Protein AtlasENSG00000127252-HRASLS [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)HRASLS
DMDM Disease mutations57110
Blocks (Seattle)HRASLS
Human Protein Atlas [tissue]ENSG00000127252-HRASLS [tissue]
HPRD07577
IPIIPI00925994   IPI00925760   
Protein Interaction databases
FunCoupENSG00000127252
BioGRIDHRASLS
STRING (EMBL)HRASLS
ZODIACHRASLS
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease57110
BioCentury BCIQHRASLS
ClinGenHRASLS
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD57110
Clinical trialHRASLS
Miscellaneous
canSAR (ICR)HRASLS (select the gene name)
DataMed IndexHRASLS
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineHRASLS
EVEXHRASLS
GoPubMedHRASLS
iHOPHRASLS
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 Feb 3 15:03:08 CET 2020

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