Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

GS1-594A7.3 (uncharacterized LOC104798195)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 104798195
Atlas_Id 77257
Location Xp22.2  [Link to chromosome band Xp22]
Location_base_pair Starts at 15602881 and ends at 15621484 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)GS1-594A7.3  104798195  uncharacterized LOC104798195
Aliases
GeneCards (Weizmann)GS1-594A7.3
Ensembl hg19 (Hinxton)ENSG00000225833 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000225833 [Gene_View]  chrX:15602881-15621484 [Contig_View]  GS1-594A7.3 [Vega]
ICGC DataPortalENSG00000225833
TCGA cBioPortalGS1-594A7.3
AceView (NCBI)GS1-594A7.3
Genatlas (Paris)GS1-594A7.3
WikiGenes104798195
SOURCE (Princeton)GS1-594A7.3
Genetics Home Reference (NIH)GS1-594A7.3
Genomic and cartography
GoldenPath hg38 (UCSC)GS1-594A7.3  -     chrX:15602881-15621484 +  Xp22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)GS1-594A7.3  -     Xp22.2   [Description]    (hg19-Feb_2009)
EnsemblGS1-594A7.3 - Xp22.2 [CytoView hg19]  GS1-594A7.3 - Xp22.2 [CytoView hg38]
Mapping of homologs : NCBIGS1-594A7.3 [Mapview hg19]  GS1-594A7.3 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BQ013720
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)GS1-594A7.3
Cluster EST : UnigeneHs.131674 [ NCBI ]
CGAP (NCI)Hs.131674
Alternative Splicing GalleryENSG00000225833
Gene ExpressionGS1-594A7.3 [ NCBI-GEO ]   GS1-594A7.3 [ EBI - ARRAY_EXPRESS ]   GS1-594A7.3 [ SEEK ]   GS1-594A7.3 [ MEM ]
Gene Expression Viewer (FireBrowse)GS1-594A7.3 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)104798195
GTEX Portal (Tissue expression)GS1-594A7.3
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)GS1-594A7.3
DMDM Disease mutations104798195
Blocks (Seattle)GS1-594A7.3
Human Protein AtlasENSG00000225833
Protein Interaction databases
FunCoupENSG00000225833
BioGRIDGS1-594A7.3
STRING (EMBL)GS1-594A7.3
ZODIACGS1-594A7.3
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease104798195
BioCentury BCIQGS1-594A7.3
ClinGenGS1-594A7.3
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD104798195
Clinical trialGS1-594A7.3
Miscellaneous
canSAR (ICR)GS1-594A7.3 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineGS1-594A7.3
EVEXGS1-594A7.3
GoPubMedGS1-594A7.3
iHOPGS1-594A7.3
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 13:09:59 CEST 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.