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LOC100288910 (uncharacterized LOC100288910)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100288910
Atlas_Id 66690
Location 14q21.3  [Link to chromosome band 14q21]
Location_base_pair Starts at 49597475 and ends at 49599164 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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100288910  100288910  uncharacterized LOC100288910
Aliases
GeneCards (Weizmann)LOC100288910
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr14:49597475-49599164 [Contig_View]  LOC100288910 [Vega]
TCGA cBioPortalLOC100288910
AceView (NCBI)LOC100288910
Genatlas (Paris)LOC100288910
WikiGenes100288910
SOURCE (Princeton)LOC100288910
Genetics Home Reference (NIH)LOC100288910
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100288910  -     chr14:49597475-49599164 -  14q21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100288910  -     14q21.3   [Description]    (hg19-Feb_2009)
EnsemblLOC100288910 - 14q21.3 [CytoView hg19]  LOC100288910 - 14q21.3 [CytoView hg38]
Mapping of homologs : NCBILOC100288910 [Mapview hg19]  LOC100288910 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX161511
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100288910
Cluster EST : UnigeneHs.156367 [ NCBI ]
CGAP (NCI)Hs.156367
Gene ExpressionLOC100288910 [ NCBI-GEO ]   LOC100288910 [ EBI - ARRAY_EXPRESS ]   LOC100288910 [ SEEK ]   LOC100288910 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100288910 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100288910
GTEX Portal (Tissue expression)LOC100288910
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100288910
DMDM Disease mutations100288910
Blocks (Seattle)LOC100288910
IPIIPI00384046   
Protein Interaction databases
BioGRIDLOC100288910
STRING (EMBL)LOC100288910
ZODIACLOC100288910
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100288910
BioCentury BCIQLOC100288910
ClinGenLOC100288910
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100288910
Clinical trialLOC100288910
Miscellaneous
canSAR (ICR)LOC100288910 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100288910
EVEXLOC100288910
GoPubMedLOC100288910
iHOPLOC100288910
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 13:48:11 CET 2017

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