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

GS1-204I12.4 (uncharacterized GS1-204I12.4)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105371653
Atlas_Id 76863
Location 1q25.3  [Link to chromosome band 1q25]
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)GS1-204I12.4  105371653  uncharacterized GS1-204I12.4
Aliases
GeneCards (Weizmann)GS1-204I12.4
Ensembl hg19 (Hinxton)ENSG00000261729 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261729 [Gene_View]  ENSG00000261729 [Sequence]  - [Contig_View]  GS1-204I12.4 [Vega]
ICGC DataPortalENSG00000261729
TCGA cBioPortalGS1-204I12.4
AceView (NCBI)GS1-204I12.4
Genatlas (Paris)GS1-204I12.4
WikiGenes105371653
SOURCE (Princeton)GS1-204I12.4
Genetics Home Reference (NIH)GS1-204I12.4
Genomic and cartography
GoldenPath hg38 (UCSC)GS1-204I12.4  -  
GoldenPath hg19 (UCSC)GS1-204I12.4  -  
GoldenPathGS1-204I12.4 - [CytoView hg19]  GS1-204I12.4 - [CytoView hg38]
ImmunoBaseENSG00000261729
genome Data Viewer NCBIGS1-204I12.4 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AF508908
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)GS1-204I12.4
Alternative Splicing GalleryENSG00000261729
Gene ExpressionGS1-204I12.4 [ NCBI-GEO ]   GS1-204I12.4 [ EBI - ARRAY_EXPRESS ]   GS1-204I12.4 [ SEEK ]   GS1-204I12.4 [ MEM ]
Gene Expression Viewer (FireBrowse)GS1-204I12.4 [ Firebrowse - Broad ]
GenevisibleExpression of GS1-204I12.4 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)105371653
GTEX Portal (Tissue expression)GS1-204I12.4
Human Protein AtlasENSG00000261729-GS1-204I12.4 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)GS1-204I12.4
DMDM Disease mutations105371653
Blocks (Seattle)GS1-204I12.4
Human Protein Atlas [tissue]ENSG00000261729-GS1-204I12.4 [tissue]
Protein Interaction databases
FunCoupENSG00000261729
BioGRIDGS1-204I12.4
STRING (EMBL)GS1-204I12.4
ZODIACGS1-204I12.4
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105371653
BioCentury BCIQGS1-204I12.4
ClinGenGS1-204I12.4
Clinical trials, drugs, therapy
Protein Interactions : CTD105371653
Clinical trialGS1-204I12.4
Miscellaneous
canSAR (ICR)GS1-204I12.4 (select the gene name)
HarmonizomeGS1-204I12.4
DataMed IndexGS1-204I12.4
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineGS1-204I12.4
EVEXGS1-204I12.4
GoPubMedGS1-204I12.4
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 : Fri Jul 10 20:04:58 CEST 2020

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.