Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100499489 (uncharacterized LOC100499489)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100499489
Atlas_Id 66734
Location 10p12.2  [Link to chromosome band 10p12]
Location_base_pair Starts at 22435425 and ends at 22437929 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)LOC100499489  100499489  uncharacterized LOC100499489
Aliases
GeneCards (Weizmann)LOC100499489
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr10:22435425-22437929 [Contig_View]  LOC100499489 [Vega]
TCGA cBioPortalLOC100499489
AceView (NCBI)LOC100499489
Genatlas (Paris)LOC100499489
WikiGenes100499489
SOURCE (Princeton)LOC100499489
Genetics Home Reference (NIH)LOC100499489
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100499489  -     chr10:22435425-22437929 -  10p12.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100499489  -     10p12.2   [Description]    (hg19-Feb_2009)
GoldenPathLOC100499489 - 10p12.2 [CytoView hg19]  LOC100499489 - 10p12.2 [CytoView hg38]
genome Data Viewer NCBILOC100499489 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AI051378 BM929412 DA867189
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100499489
Gene ExpressionLOC100499489 [ NCBI-GEO ]   LOC100499489 [ EBI - ARRAY_EXPRESS ]   LOC100499489 [ SEEK ]   LOC100499489 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100499489 [ Firebrowse - Broad ]
GenevisibleExpression of LOC100499489 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100499489
GTEX Portal (Tissue expression)LOC100499489
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100499489
DMDM Disease mutations100499489
Blocks (Seattle)LOC100499489
Protein Interaction databases
BioGRIDLOC100499489
STRING (EMBL)LOC100499489
ZODIACLOC100499489
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100499489
BioCentury BCIQLOC100499489
ClinGenLOC100499489
Clinical trials, drugs, therapy
Protein Interactions : CTD100499489
Clinical trialLOC100499489
Miscellaneous
canSAR (ICR)LOC100499489 (select the gene name)
HarmonizomeLOC100499489
DataMed IndexLOC100499489
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100499489
EVEXLOC100499489
GoPubMedLOC100499489
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 : Fri Jul 10 20:15:20 CEST 2020

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