Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927699 (uncharacterized LOC101927699)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927699
Atlas_Id 80562
Location 10q11.22  [Link to chromosome band 10q11]
Location_base_pair Starts at 46596104 and ends at 46598145 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)LOC101927699  101927699  uncharacterized LOC101927699
Aliases
GeneCards (Weizmann)LOC101927699
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]   [Sequence]  chr10:46596104-46598145 [Contig_View]  LOC101927699 [Vega]
TCGA cBioPortalLOC101927699
AceView (NCBI)LOC101927699
Genatlas (Paris)LOC101927699
WikiGenes101927699
SOURCE (Princeton)LOC101927699
Genetics Home Reference (NIH)LOC101927699
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927699  -     chr10:46596104-46598145 -  10q11.22   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927699  -     10q11.22   [Description]    (hg19-Feb_2009)
GoldenPathLOC101927699 - 10q11.22 [CytoView hg19]  LOC101927699 - 10q11.22 [CytoView hg38]
Mapping of homologs : NCBILOC101927699 [Mapview hg19]  LOC101927699 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA583561 CA440170 DA417562 DA515489 DA769348
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927699
Cluster EST : UnigeneHs.663831 [ NCBI ]
CGAP (NCI)Hs.663831
Gene ExpressionLOC101927699 [ NCBI-GEO ]   LOC101927699 [ EBI - ARRAY_EXPRESS ]   LOC101927699 [ SEEK ]   LOC101927699 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927699 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927699
GTEX Portal (Tissue expression)LOC101927699
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927699
DMDM Disease mutations101927699
Blocks (Seattle)LOC101927699
Protein Interaction databases
BioGRIDLOC101927699
STRING (EMBL)LOC101927699
ZODIACLOC101927699
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927699
BioCentury BCIQLOC101927699
ClinGenLOC101927699
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927699
Clinical trialLOC101927699
Miscellaneous
canSAR (ICR)LOC101927699 (select the gene name)
DataMed IndexLOC101927699
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927699
EVEXLOC101927699
GoPubMedLOC101927699
iHOPLOC101927699
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 Sep 3 15:43:16 CEST 2019

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