Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927851 (uncharacterized LOC101927851)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927851
Atlas_Id 67234
Location 1q42.3  [Link to chromosome band 1q42]
Location_base_pair Starts at 234957343 and ends at 234963999 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)LOC101927851  101927851  uncharacterized LOC101927851
Aliases
GeneCards (Weizmann)LOC101927851
Ensembl hg19 (Hinxton)ENSG00000238005 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000238005 [Gene_View]  chr1:234957343-234963999 [Contig_View]  LOC101927851 [Vega]
ICGC DataPortalENSG00000238005
TCGA cBioPortalLOC101927851
AceView (NCBI)LOC101927851
Genatlas (Paris)LOC101927851
WikiGenes101927851
SOURCE (Princeton)LOC101927851
Genetics Home Reference (NIH)LOC101927851
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927851  -     chr1:234957343-234963999 -  1q42.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927851  -     1q42.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101927851 - 1q42.3 [CytoView hg19]  LOC101927851 - 1q42.3 [CytoView hg38]
Mapping of homologs : NCBILOC101927851 [Mapview hg19]  LOC101927851 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC016972
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927851
Cluster EST : UnigeneHs.520684 [ NCBI ]
CGAP (NCI)Hs.520684
Alternative Splicing GalleryENSG00000238005
Gene ExpressionLOC101927851 [ NCBI-GEO ]   LOC101927851 [ EBI - ARRAY_EXPRESS ]   LOC101927851 [ SEEK ]   LOC101927851 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927851 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927851
GTEX Portal (Tissue expression)LOC101927851
Human Protein AtlasENSG00000238005-LOC101927851 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927851
DMDM Disease mutations101927851
Blocks (Seattle)LOC101927851
Human Protein Atlas [tissue]ENSG00000238005-LOC101927851 [tissue]
Protein Interaction databases
FunCoupENSG00000238005
BioGRIDLOC101927851
STRING (EMBL)LOC101927851
ZODIACLOC101927851
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927851
BioCentury BCIQLOC101927851
ClinGenLOC101927851
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927851
Clinical trialLOC101927851
Miscellaneous
canSAR (ICR)LOC101927851 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927851
EVEXLOC101927851
GoPubMedLOC101927851
iHOPLOC101927851
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 Nov 21 13:50:32 CET 2017

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