Atlas of Genetics and Cytogenetics in Oncology and Haematology

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LOC101928902 (uncharacterized LOC101928902)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928902
Atlas_Id 77085
Location 8q24.3  [Link to chromosome band 8q24]
Location_base_pair Starts at 144368937 and ends at 144372871 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)LOC101928902  101928902  uncharacterized LOC101928902
Aliases
GeneCards (Weizmann)LOC101928902
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr8:144368937-144372871 [Contig_View]  LOC101928902 [Vega]
TCGA cBioPortalLOC101928902
AceView (NCBI)LOC101928902
Genatlas (Paris)LOC101928902
WikiGenes101928902
SOURCE (Princeton)LOC101928902
Genetics Home Reference (NIH)LOC101928902
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928902  -     chr8:144368937-144372871 -  8q24.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928902  -     8q24.3   [Description]    (hg19-Feb_2009)
GoldenPathLOC101928902 - 8q24.3 [CytoView hg19]  LOC101928902 - 8q24.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928902 [Mapview hg19]  LOC101928902 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC026857 BC035862 BC047297
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928902
Gene ExpressionLOC101928902 [ NCBI-GEO ]   LOC101928902 [ EBI - ARRAY_EXPRESS ]   LOC101928902 [ SEEK ]   LOC101928902 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928902 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928902
GTEX Portal (Tissue expression)LOC101928902
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928902
DMDM Disease mutations101928902
Blocks (Seattle)LOC101928902
Protein Interaction databases
BioGRIDLOC101928902
STRING (EMBL)LOC101928902
ZODIACLOC101928902
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928902
BioCentury BCIQLOC101928902
ClinGenLOC101928902
Clinical trials, drugs, therapy
Protein Interactions : CTD101928902
Clinical trialLOC101928902
Miscellaneous
canSAR (ICR)LOC101928902 (select the gene name)
HarmonizomeLOC101928902
DataMed IndexLOC101928902
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928902
EVEXLOC101928902
GoPubMedLOC101928902
iHOPLOC101928902
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 Jun 30 19:48:57 CEST 2020
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