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

LOC283887 (uncharacterized LOC283887)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 283887
Atlas_Id 67916
Location 16p12.1  [Link to chromosome band 16p12]
Location_base_pair Starts at 25078359 and ends at 25080275 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)LOC283887  283887  uncharacterized LOC283887
Aliases
GeneCards (Weizmann)LOC283887
Ensembl hg19 (Hinxton)ENSG00000262155 [Gene_View]  chr16:25078359-25080275 [Contig_View]  LOC283887 [Vega]
Ensembl hg38 (Hinxton)ENSG00000262155 [Gene_View]  chr16:25078359-25080275 [Contig_View]  LOC283887 [Vega]
ICGC DataPortalENSG00000262155
TCGA cBioPortalLOC283887
AceView (NCBI)LOC283887
Genatlas (Paris)LOC283887
WikiGenes283887
SOURCE (Princeton)LOC283887
Genetics Home Reference (NIH)LOC283887
Genomic and cartography
GoldenPath hg19 (UCSC)LOC283887  -     chr16:25078359-25080275 +  16p12.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC283887  -     16p12.1   [Description]    (hg38-Dec_2013)
EnsemblLOC283887 - 16p12.1 [CytoView hg19]  LOC283887 - 16p12.1 [CytoView hg38]
Mapping of homologs : NCBILOC283887 [Mapview hg19]  LOC283887 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK093382 BC023651 HG507864
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000016 NC_018927 NT_187260 NW_004929400
Consensus coding sequences : CCDS (NCBI)LOC283887
Cluster EST : UnigeneHs.652665 [ NCBI ]
CGAP (NCI)Hs.652665
Alternative Splicing GalleryENSG00000262155
Gene ExpressionLOC283887 [ NCBI-GEO ]   LOC283887 [ EBI - ARRAY_EXPRESS ]   LOC283887 [ SEEK ]   LOC283887 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC283887 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)283887
GTEX Portal (Tissue expression)LOC283887
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC283887
DMDM Disease mutations283887
Blocks (Seattle)LOC283887
Human Protein AtlasENSG00000262155
Protein Interaction databases
FunCoupENSG00000262155
BioGRIDLOC283887
STRING (EMBL)LOC283887
ZODIACLOC283887
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease283887
BioCentury BCIQLOC283887
ClinGenLOC283887
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD283887
Clinical trialLOC283887
Miscellaneous
canSAR (ICR)LOC283887 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC283887
EVEXLOC283887
GoPubMedLOC283887
iHOPLOC283887
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 12:24:32 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.