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LOC107984784 (uncharacterized LOC107984784)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 107984784
Atlas_Id 79851
Location 15q22.2  [Link to chromosome band 15q22]
Location_base_pair Starts at 62196172 and ends at 62203318 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)LOC107984784  107984784  uncharacterized LOC107984784
Aliases
GeneCards (Weizmann)LOC107984784
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr15:62196172-62203318 [Contig_View]  LOC107984784 [Vega]
TCGA cBioPortalLOC107984784
AceView (NCBI)LOC107984784
Genatlas (Paris)LOC107984784
WikiGenes107984784
SOURCE (Princeton)LOC107984784
Genetics Home Reference (NIH)LOC107984784
Genomic and cartography
GoldenPath hg38 (UCSC)LOC107984784  -     chr15:62196172-62203318 -  15q22.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC107984784  -     15q22.2   [Description]    (hg19-Feb_2009)
EnsemblLOC107984784 - 15q22.2 [CytoView hg19]  LOC107984784 - 15q22.2 [CytoView hg38]
Mapping of homologs : NCBILOC107984784 [Mapview hg19]  LOC107984784 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC031230
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC107984784
Cluster EST : UnigeneHs.591131 [ NCBI ]
CGAP (NCI)Hs.591131
Gene ExpressionLOC107984784 [ NCBI-GEO ]   LOC107984784 [ EBI - ARRAY_EXPRESS ]   LOC107984784 [ SEEK ]   LOC107984784 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC107984784 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)107984784
GTEX Portal (Tissue expression)LOC107984784
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC107984784
DMDM Disease mutations107984784
Blocks (Seattle)LOC107984784
Protein Interaction databases
BioGRIDLOC107984784
STRING (EMBL)LOC107984784
ZODIACLOC107984784
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease107984784
BioCentury BCIQLOC107984784
ClinGenLOC107984784
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD107984784
Clinical trialLOC107984784
Miscellaneous
canSAR (ICR)LOC107984784 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC107984784
EVEXLOC107984784
GoPubMedLOC107984784
iHOPLOC107984784
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 13:55:32 CET 2017

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