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

LOC101929698 (uncharacterized LOC101929698)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929698
Atlas_Id 67616
Location 20q11.21  [Link to chromosome band 20q11]
Location_base_pair Starts at 32509959 and ends at 32520285 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)LOC101929698  101929698  uncharacterized LOC101929698
Aliases
GeneCards (Weizmann)LOC101929698
Ensembl hg19 (Hinxton)ENSG00000277301 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000277301 [Gene_View]  chr20:32509959-32520285 [Contig_View]  LOC101929698 [Vega]
ICGC DataPortalENSG00000277301
TCGA cBioPortalLOC101929698
AceView (NCBI)LOC101929698
Genatlas (Paris)LOC101929698
WikiGenes101929698
SOURCE (Princeton)LOC101929698
Genetics Home Reference (NIH)LOC101929698
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929698  -     chr20:32509959-32520285 +  20q11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929698  -     20q11.21   [Description]    (hg19-Feb_2009)
EnsemblLOC101929698 - 20q11.21 [CytoView hg19]  LOC101929698 - 20q11.21 [CytoView hg38]
Mapping of homologs : NCBILOC101929698 [Mapview hg19]  LOC101929698 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK097865
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929698
Cluster EST : UnigeneHs.638392 [ NCBI ]
CGAP (NCI)Hs.638392
Alternative Splicing GalleryENSG00000277301
Gene ExpressionLOC101929698 [ NCBI-GEO ]   LOC101929698 [ EBI - ARRAY_EXPRESS ]   LOC101929698 [ SEEK ]   LOC101929698 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929698 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929698
GTEX Portal (Tissue expression)LOC101929698
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929698
DMDM Disease mutations101929698
Blocks (Seattle)LOC101929698
Human Protein AtlasENSG00000277301
Protein Interaction databases
FunCoupENSG00000277301
BioGRIDLOC101929698
STRING (EMBL)LOC101929698
ZODIACLOC101929698
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929698
BioCentury BCIQLOC101929698
ClinGenLOC101929698
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929698
Clinical trialLOC101929698
Miscellaneous
canSAR (ICR)LOC101929698 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929698
EVEXLOC101929698
GoPubMedLOC101929698
iHOPLOC101929698
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 16:06:39 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.