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

LOC101927553 (-)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927553
Atlas_Id 77520
Location -  [Link to chromosome band ]
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)LOC101927553  101927553  -
Aliases
GeneCards (Weizmann)LOC101927553
Ensembl hg19 (Hinxton)ENSG00000232964 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000232964 [Gene_View]  - [Contig_View]  LOC101927553 [Vega]
ICGC DataPortalENSG00000232964
TCGA cBioPortalLOC101927553
AceView (NCBI)LOC101927553
Genatlas (Paris)LOC101927553
WikiGenes101927553
SOURCE (Princeton)LOC101927553
Genetics Home Reference (NIH)LOC101927553
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927553  -  
GoldenPath hg19 (UCSC)LOC101927553  -  
EnsemblLOC101927553 - [CytoView hg19]  LOC101927553 - [CytoView hg38]
Mapping of homologs : NCBILOC101927553 [Mapview hg19]  LOC101927553 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927553
Alternative Splicing GalleryENSG00000232964
Gene ExpressionLOC101927553 [ NCBI-GEO ]   LOC101927553 [ EBI - ARRAY_EXPRESS ]   LOC101927553 [ SEEK ]   LOC101927553 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927553 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927553
GTEX Portal (Tissue expression)LOC101927553
Human Protein AtlasENSG00000232964-LOC101927553 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927553
DMDM Disease mutations101927553
Blocks (Seattle)LOC101927553
Human Protein Atlas [tissue]ENSG00000232964-LOC101927553 [tissue]
Protein Interaction databases
FunCoupENSG00000232964
BioGRIDLOC101927553
STRING (EMBL)LOC101927553
ZODIACLOC101927553
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927553
BioCentury BCIQLOC101927553
ClinGenLOC101927553
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927553
Clinical trialLOC101927553
Miscellaneous
canSAR (ICR)LOC101927553 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927553
EVEXLOC101927553
GoPubMedLOC101927553
iHOPLOC101927553
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 : Thu Nov 9 12:03:23 CET 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.