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LOC105372028 (uncharacterized LOC105372028)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 105372028
Atlas_Id 78181
Location 18q11.2  [Link to chromosome band 18q11]
Location_base_pair Starts at 24725781 and ends at 24766645 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)LOC105372028  105372028  uncharacterized LOC105372028
Aliases
GeneCards (Weizmann)LOC105372028
Ensembl hg19 (Hinxton)ENSG00000266573 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000266573 [Gene_View]  chr18:24725781-24766645 [Contig_View]  LOC105372028 [Vega]
ICGC DataPortalENSG00000266573
TCGA cBioPortalLOC105372028
AceView (NCBI)LOC105372028
Genatlas (Paris)LOC105372028
WikiGenes105372028
SOURCE (Princeton)LOC105372028
Genetics Home Reference (NIH)LOC105372028
Genomic and cartography
GoldenPath hg38 (UCSC)LOC105372028  -     chr18:24725781-24766645 +  18q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC105372028  -     18q11.2   [Description]    (hg19-Feb_2009)
EnsemblLOC105372028 - 18q11.2 [CytoView hg19]  LOC105372028 - 18q11.2 [CytoView hg38]
Mapping of homologs : NCBILOC105372028 [Mapview hg19]  LOC105372028 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DA128369
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC105372028
Cluster EST : UnigeneHs.569901 [ NCBI ]
CGAP (NCI)Hs.569901
Alternative Splicing GalleryENSG00000266573
Gene ExpressionLOC105372028 [ NCBI-GEO ]   LOC105372028 [ EBI - ARRAY_EXPRESS ]   LOC105372028 [ SEEK ]   LOC105372028 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC105372028 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)105372028
GTEX Portal (Tissue expression)LOC105372028
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC105372028
DMDM Disease mutations105372028
Blocks (Seattle)LOC105372028
Human Protein AtlasENSG00000266573
Protein Interaction databases
FunCoupENSG00000266573
BioGRIDLOC105372028
STRING (EMBL)LOC105372028
ZODIACLOC105372028
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease105372028
BioCentury BCIQLOC105372028
ClinGenLOC105372028
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD105372028
Clinical trialLOC105372028
Miscellaneous
canSAR (ICR)LOC105372028 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC105372028
EVEXLOC105372028
GoPubMedLOC105372028
iHOPLOC105372028
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 : Mon Sep 18 13:23:11 CEST 2017

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