Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   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

LOC101929707 (uncharacterized LOC101929707)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929707
Atlas_Id 67619
Location 20p11.21  [Link to chromosome band 20p11]
Location_base_pair Starts at 22987308 and ends at 23011422 bp from pter ( according to hg19-Feb_2009)
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)LOC101929707  101929707  uncharacterized LOC101929707
Aliases
GeneCards (Weizmann)LOC101929707
Ensembl hg19 (Hinxton) [Gene_View]  chr20:22987308-23011422 [Contig_View]  LOC101929707 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr20:22987308-23011422 [Contig_View]  LOC101929707 [Vega]
TCGA cBioPortalLOC101929707
AceView (NCBI)LOC101929707
Genatlas (Paris)LOC101929707
WikiGenes101929707
SOURCE (Princeton)LOC101929707
Genetics Home Reference (NIH)LOC101929707
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101929707  -     chr20:22987308-23011422 -  20p11.21   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101929707  -     20p11.21   [Description]    (hg38-Dec_2013)
EnsemblLOC101929707 - 20p11.21 [CytoView hg19]  LOC101929707 - 20p11.21 [CytoView hg38]
Mapping of homologs : NCBILOC101929707 [Mapview hg19]  LOC101929707 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC045663 HG511259
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000020 NC_018931 NT_011387 NW_004929416
Consensus coding sequences : CCDS (NCBI)LOC101929707
Cluster EST : UnigeneHs.542406 [ NCBI ]
CGAP (NCI)Hs.542406
Gene ExpressionLOC101929707 [ NCBI-GEO ]   LOC101929707 [ EBI - ARRAY_EXPRESS ]   LOC101929707 [ SEEK ]   LOC101929707 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929707 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929707
GTEX Portal (Tissue expression)LOC101929707
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929707
DMDM Disease mutations101929707
Blocks (Seattle)LOC101929707
Protein Interaction databases
BioGRIDLOC101929707
STRING (EMBL)LOC101929707
ZODIACLOC101929707
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929707
BioCentury BCIQLOC101929707
ClinGenLOC101929707
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929707
Clinical trialLOC101929707
Miscellaneous
canSAR (ICR)LOC101929707 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929707
EVEXLOC101929707
GoPubMedLOC101929707
iHOPLOC101929707
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 Mar 14 12:20:55 CET 2017

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

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.