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

LOC101929754 (-)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929754
Atlas_Id 67631
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)LOC101929754  101929754  -
Aliases
GeneCards (Weizmann)LOC101929754
Ensembl hg19 (Hinxton)ENSG00000242290 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000242290 [Gene_View]  - [Contig_View]  LOC101929754 [Vega]
ICGC DataPortalENSG00000242290
TCGA cBioPortalLOC101929754
AceView (NCBI)LOC101929754
Genatlas (Paris)LOC101929754
WikiGenes101929754
SOURCE (Princeton)LOC101929754
Genetics Home Reference (NIH)LOC101929754
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929754  -  
GoldenPath hg19 (UCSC)LOC101929754  -  
EnsemblLOC101929754 - [CytoView hg19]  LOC101929754 - [CytoView hg38]
Mapping of homologs : NCBILOC101929754 [Mapview hg19]  LOC101929754 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929754
Alternative Splicing GalleryENSG00000242290
Gene ExpressionLOC101929754 [ NCBI-GEO ]   LOC101929754 [ EBI - ARRAY_EXPRESS ]   LOC101929754 [ SEEK ]   LOC101929754 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929754 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929754
GTEX Portal (Tissue expression)LOC101929754
Human Protein AtlasENSG00000242290-LOC101929754 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929754
DMDM Disease mutations101929754
Blocks (Seattle)LOC101929754
Human Protein Atlas [tissue]ENSG00000242290-LOC101929754 [tissue]
Protein Interaction databases
FunCoupENSG00000242290
BioGRIDLOC101929754
STRING (EMBL)LOC101929754
ZODIACLOC101929754
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929754
BioCentury BCIQLOC101929754
ClinGenLOC101929754
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929754
Clinical trialLOC101929754
Miscellaneous
canSAR (ICR)LOC101929754 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929754
EVEXLOC101929754
GoPubMedLOC101929754
iHOPLOC101929754
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 : Tue Nov 21 13:52:28 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.