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

LOC101929526 (uncharacterized LOC101929526)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929526
Atlas_Id 67575
Location 20p11.23  [Link to chromosome band 20p11]
Location_base_pair Starts at 18674395 and ends at 18698708 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)LOC101929526  101929526  uncharacterized LOC101929526
Aliases
GeneCards (Weizmann)LOC101929526
Ensembl hg19 (Hinxton)ENSG00000233993 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000233993 [Gene_View]  chr20:18674395-18698708 [Contig_View]  LOC101929526 [Vega]
ICGC DataPortalENSG00000233993
TCGA cBioPortalLOC101929526
AceView (NCBI)LOC101929526
Genatlas (Paris)LOC101929526
WikiGenes101929526
SOURCE (Princeton)LOC101929526
Genetics Home Reference (NIH)LOC101929526
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929526  -     chr20:18674395-18698708 -  20p11.23   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929526  -     20p11.23   [Description]    (hg19-Feb_2009)
EnsemblLOC101929526 - 20p11.23 [CytoView hg19]  LOC101929526 - 20p11.23 [CytoView hg38]
Mapping of homologs : NCBILOC101929526 [Mapview hg19]  LOC101929526 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC042559
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929526
Cluster EST : UnigeneHs.639402 [ NCBI ]
CGAP (NCI)Hs.639402
Alternative Splicing GalleryENSG00000233993
Gene ExpressionLOC101929526 [ NCBI-GEO ]   LOC101929526 [ EBI - ARRAY_EXPRESS ]   LOC101929526 [ SEEK ]   LOC101929526 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929526 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929526
GTEX Portal (Tissue expression)LOC101929526
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929526
DMDM Disease mutations101929526
Blocks (Seattle)LOC101929526
Human Protein AtlasENSG00000233993
Protein Interaction databases
FunCoupENSG00000233993
BioGRIDLOC101929526
STRING (EMBL)LOC101929526
ZODIACLOC101929526
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929526
BioCentury BCIQLOC101929526
ClinGenLOC101929526
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929526
Clinical trialLOC101929526
Miscellaneous
canSAR (ICR)LOC101929526 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929526
EVEXLOC101929526
GoPubMedLOC101929526
iHOPLOC101929526
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 : Wed Jun 7 16:06:27 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.