Atlas of Genetics and Cytogenetics in Oncology and Haematology


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GS1-600G8.3 (unknown transcript)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100093698
Atlas_Id 64068
Location Xp22.2  [Link to chromosome band Xp22]
Location_base_pair Starts at 13328771 and ends at 13338052 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)GS1-600G8.3  100093698  unknown transcript
Aliases
GeneCards (Weizmann)GS1-600G8.3
Ensembl hg19 (Hinxton)ENSG00000231216 [Gene_View]  chrX:13328771-13338052 [Contig_View]  GS1-600G8.3 [Vega]
Ensembl hg38 (Hinxton)ENSG00000231216 [Gene_View]  chrX:13328771-13338052 [Contig_View]  GS1-600G8.3 [Vega]
ICGC DataPortalENSG00000231216
TCGA cBioPortalGS1-600G8.3
AceView (NCBI)GS1-600G8.3
Genatlas (Paris)GS1-600G8.3
WikiGenes100093698
SOURCE (Princeton)GS1-600G8.3
Genetics Home Reference (NIH)GS1-600G8.3
Genomic and cartography
GoldenPath hg19 (UCSC)GS1-600G8.3  -     chrX:13328771-13338052 +  Xp22.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)GS1-600G8.3  -     Xp22.2   [Description]    (hg38-Dec_2013)
EnsemblGS1-600G8.3 - Xp22.2 [CytoView hg19]  GS1-600G8.3 - Xp22.2 [CytoView hg38]
Mapping of homologs : NCBIGS1-600G8.3 [Mapview hg19]  GS1-600G8.3 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC022040 BG720643 HG512441
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000023 NC_018934 NT_167197 NW_004929438
Consensus coding sequences : CCDS (NCBI)GS1-600G8.3
Cluster EST : UnigeneHs.643612 [ NCBI ]
CGAP (NCI)Hs.643612
Alternative Splicing GalleryENSG00000231216
Gene ExpressionGS1-600G8.3 [ NCBI-GEO ]   GS1-600G8.3 [ EBI - ARRAY_EXPRESS ]   GS1-600G8.3 [ SEEK ]   GS1-600G8.3 [ MEM ]
Gene Expression Viewer (FireBrowse)GS1-600G8.3 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100093698
GTEX Portal (Tissue expression)GS1-600G8.3
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)GS1-600G8.3
DMDM Disease mutations100093698
Blocks (Seattle)GS1-600G8.3
Human Protein AtlasENSG00000231216
Protein Interaction databases
FunCoupENSG00000231216
BioGRIDGS1-600G8.3
STRING (EMBL)GS1-600G8.3
ZODIACGS1-600G8.3
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100093698
BioCentury BCIQGS1-600G8.3
ClinGenGS1-600G8.3
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100093698
Clinical trialGS1-600G8.3
Miscellaneous
canSAR (ICR)GS1-600G8.3 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGS1-600G8.3
EVEXGS1-600G8.3
GoPubMedGS1-600G8.3
iHOPGS1-600G8.3
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 12:07:02 CET 2017

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