Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928937 (uncharacterized LOC101928937)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928937
Atlas_Id 67462
Location 12q23.1  [Link to chromosome band 12q23]
Location_base_pair Starts at 99093359 and ends at 99105011 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)LOC101928937  101928937  uncharacterized LOC101928937
Aliases
GeneCards (Weizmann)LOC101928937
Ensembl hg19 (Hinxton)ENSG00000258039 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258039 [Gene_View]  chr12:99093359-99105011 [Contig_View]  LOC101928937 [Vega]
ICGC DataPortalENSG00000258039
TCGA cBioPortalLOC101928937
AceView (NCBI)LOC101928937
Genatlas (Paris)LOC101928937
WikiGenes101928937
SOURCE (Princeton)LOC101928937
Genetics Home Reference (NIH)LOC101928937
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928937  -     chr12:99093359-99105011 +  12q23.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928937  -     12q23.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101928937 - 12q23.1 [CytoView hg19]  LOC101928937 - 12q23.1 [CytoView hg38]
Mapping of homologs : NCBILOC101928937 [Mapview hg19]  LOC101928937 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC043545
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928937
Cluster EST : UnigeneHs.555499 [ NCBI ]
CGAP (NCI)Hs.555499
Alternative Splicing GalleryENSG00000258039
Gene ExpressionLOC101928937 [ NCBI-GEO ]   LOC101928937 [ EBI - ARRAY_EXPRESS ]   LOC101928937 [ SEEK ]   LOC101928937 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928937 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928937
GTEX Portal (Tissue expression)LOC101928937
Human Protein AtlasENSG00000258039-LOC101928937 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928937
DMDM Disease mutations101928937
Blocks (Seattle)LOC101928937
Human Protein Atlas [tissue]ENSG00000258039-LOC101928937 [tissue]
Protein Interaction databases
FunCoupENSG00000258039
BioGRIDLOC101928937
STRING (EMBL)LOC101928937
ZODIACLOC101928937
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928937
BioCentury BCIQLOC101928937
ClinGenLOC101928937
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928937
Clinical trialLOC101928937
Miscellaneous
canSAR (ICR)LOC101928937 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928937
EVEXLOC101928937
GoPubMedLOC101928937
iHOPLOC101928937
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Thu Nov 9 12:04:51 CET 2017

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