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

LOC101927132 (uncharacterized LOC101927132)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927132
Atlas_Id 67061
Location 16q12.1  [Link to chromosome band 16q12]
Location_base_pair Starts at 47892492 and ends at 47942342 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)LOC101927132  101927132  uncharacterized LOC101927132
Aliases
GeneCards (Weizmann)LOC101927132
Ensembl hg19 (Hinxton)ENSG00000261231 [Gene_View]  chr16:47892492-47942342 [Contig_View]  LOC101927132 [Vega]
Ensembl hg38 (Hinxton)ENSG00000261231 [Gene_View]  chr16:47892492-47942342 [Contig_View]  LOC101927132 [Vega]
ICGC DataPortalENSG00000261231
TCGA cBioPortalLOC101927132
AceView (NCBI)LOC101927132
Genatlas (Paris)LOC101927132
WikiGenes101927132
SOURCE (Princeton)LOC101927132
Genetics Home Reference (NIH)LOC101927132
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101927132  -     chr16:47892492-47942342 +  16q12.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101927132  -     16q12.1   [Description]    (hg38-Dec_2013)
EnsemblLOC101927132 - 16q12.1 [CytoView hg19]  LOC101927132 - 16q12.1 [CytoView hg38]
Mapping of homologs : NCBILOC101927132 [Mapview hg19]  LOC101927132 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK091370 HG508019 HG508020
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000016 NC_018927 NT_010498 NW_004929402
Consensus coding sequences : CCDS (NCBI)LOC101927132
Cluster EST : UnigeneHs.589404 [ NCBI ]
CGAP (NCI)Hs.589404
Alternative Splicing GalleryENSG00000261231
Gene ExpressionLOC101927132 [ NCBI-GEO ]   LOC101927132 [ EBI - ARRAY_EXPRESS ]   LOC101927132 [ SEEK ]   LOC101927132 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927132 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927132
GTEX Portal (Tissue expression)LOC101927132
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927132
DMDM Disease mutations101927132
Blocks (Seattle)LOC101927132
Human Protein AtlasENSG00000261231
Protein Interaction databases
FunCoupENSG00000261231
BioGRIDLOC101927132
STRING (EMBL)LOC101927132
ZODIACLOC101927132
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927132
BioCentury BCIQLOC101927132
ClinGenLOC101927132
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927132
Clinical trialLOC101927132
Miscellaneous
canSAR (ICR)LOC101927132 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927132
EVEXLOC101927132
GoPubMedLOC101927132
iHOPLOC101927132
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 12:18:11 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.