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

LOC101928796 (uncharacterized LOC101928796)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928796
Atlas_Id 67434
Location 21q22.3  [Link to chromosome band 21q22]
Location_base_pair Starts at 47392884 and ends at 47394867 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC101928796  101928796  uncharacterized LOC101928796
Aliases
GeneCards (Weizmann)LOC101928796
Ensembl hg19 (Hinxton) [Gene_View]  chr21:47392884-47394867 [Contig_View]  LOC101928796 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr21:47392884-47394867 [Contig_View]  LOC101928796 [Vega]
TCGA cBioPortalLOC101928796
AceView (NCBI)LOC101928796
Genatlas (Paris)LOC101928796
WikiGenes101928796
SOURCE (Princeton)LOC101928796
Genetics Home Reference (NIH)LOC101928796
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101928796  -     chr21:47392884-47394867 +  21q22.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101928796  -     21q22.3   [Description]    (hg38-Dec_2013)
EnsemblLOC101928796 - 21q22.3 [CytoView hg19]  LOC101928796 - 21q22.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928796 [Mapview hg19]  LOC101928796 [Mapview hg38]
Gene and transcription
Genbank (Entrez)HY013646 LK937865
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000021 NC_018932 NT_011512 NW_004929427
Consensus coding sequences : CCDS (NCBI)LOC101928796
Cluster EST : UnigeneHs.130919 [ NCBI ]
CGAP (NCI)Hs.130919
Gene ExpressionLOC101928796 [ NCBI-GEO ]   LOC101928796 [ EBI - ARRAY_EXPRESS ]   LOC101928796 [ SEEK ]   LOC101928796 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928796 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928796
GTEX Portal (Tissue expression)LOC101928796
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928796
DMDM Disease mutations101928796
Blocks (Seattle)LOC101928796
Protein Interaction databases
BioGRIDLOC101928796
STRING (EMBL)LOC101928796
ZODIACLOC101928796
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928796
BioCentury BCIQLOC101928796
ClinGenLOC101928796
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928796
Clinical trialLOC101928796
Miscellaneous
canSAR (ICR)LOC101928796 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928796
EVEXLOC101928796
GoPubMedLOC101928796
iHOPLOC101928796
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 12:20:02 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.