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

LOC145783 (uncharacterized LOC145783)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 145783
Atlas_Id 67792
Location 15q21.3  [Link to chromosome band 15q21]
Location_base_pair Starts at 57178368 and ends at 57210697 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)LOC145783  145783  uncharacterized LOC145783
Aliases
GeneCards (Weizmann)LOC145783
Ensembl hg19 (Hinxton)ENSG00000137871 [Gene_View]  chr15:57178368-57210697 [Contig_View]  LOC145783 [Vega]
Ensembl hg38 (Hinxton)ENSG00000137871 [Gene_View]  chr15:57178368-57210697 [Contig_View]  LOC145783 [Vega]
ICGC DataPortalENSG00000137871
TCGA cBioPortalLOC145783
AceView (NCBI)LOC145783
Genatlas (Paris)LOC145783
WikiGenes145783
SOURCE (Princeton)LOC145783
Genetics Home Reference (NIH)LOC145783
Genomic and cartography
GoldenPath hg19 (UCSC)LOC145783  -     chr15:57178368-57210697 -  15q21.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC145783  -     15q21.3   [Description]    (hg38-Dec_2013)
EnsemblLOC145783 - 15q21.3 [CytoView hg19]  LOC145783 - 15q21.3 [CytoView hg38]
Mapping of homologs : NCBILOC145783 [Mapview hg19]  LOC145783 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK056606 AK096657 BC063546
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000015 NC_018926 NT_010194 NW_004929398
Consensus coding sequences : CCDS (NCBI)LOC145783
Cluster EST : UnigeneHs.620525 [ NCBI ]
CGAP (NCI)Hs.620525
Alternative Splicing GalleryENSG00000137871
Gene ExpressionLOC145783 [ NCBI-GEO ]   LOC145783 [ EBI - ARRAY_EXPRESS ]   LOC145783 [ SEEK ]   LOC145783 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC145783 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)145783
GTEX Portal (Tissue expression)LOC145783
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC145783
DMDM Disease mutations145783
Blocks (Seattle)LOC145783
Human Protein AtlasENSG00000137871
IPIIPI00976976   
Protein Interaction databases
FunCoupENSG00000137871
BioGRIDLOC145783
STRING (EMBL)LOC145783
ZODIACLOC145783
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease145783
BioCentury BCIQLOC145783
ClinGenLOC145783
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD145783
Clinical trialLOC145783
Miscellaneous
canSAR (ICR)LOC145783 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC145783
EVEXLOC145783
GoPubMedLOC145783
iHOPLOC145783
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 12:24:07 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.