Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929297 (uncharacterized LOC101929297)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929297
Atlas_Id 67532
Location 6q27  [Link to chromosome band 6q27]
Location_base_pair Starts at 166236969 and ends at 166256944 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)LOC101929297  101929297  uncharacterized LOC101929297
Aliases
GeneCards (Weizmann)LOC101929297
Ensembl hg19 (Hinxton)ENSG00000233365 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000233365 [Gene_View]  ENSG00000233365 [Sequence]  chr6:166236969-166256944 [Contig_View]  LOC101929297 [Vega]
ICGC DataPortalENSG00000233365
TCGA cBioPortalLOC101929297
AceView (NCBI)LOC101929297
Genatlas (Paris)LOC101929297
WikiGenes101929297
SOURCE (Princeton)LOC101929297
Genetics Home Reference (NIH)LOC101929297
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929297  -     chr6:166236969-166256944 +  6q27   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929297  -     6q27   [Description]    (hg19-Feb_2009)
EnsemblLOC101929297 - 6q27 [CytoView hg19]  LOC101929297 - 6q27 [CytoView hg38]
Mapping of homologs : NCBILOC101929297 [Mapview hg19]  LOC101929297 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC040873
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000006 NC_018917 NT_187557
Consensus coding sequences : CCDS (NCBI)LOC101929297
Cluster EST : UnigeneHs.434661 [ NCBI ]
CGAP (NCI)Hs.434661
Alternative Splicing GalleryENSG00000233365
Gene ExpressionLOC101929297 [ NCBI-GEO ]   LOC101929297 [ EBI - ARRAY_EXPRESS ]   LOC101929297 [ SEEK ]   LOC101929297 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929297 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929297
GTEX Portal (Tissue expression)LOC101929297
Human Protein AtlasENSG00000233365-LOC101929297 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929297
DMDM Disease mutations101929297
Blocks (Seattle)LOC101929297
Human Protein Atlas [tissue]ENSG00000233365-LOC101929297 [tissue]
Protein Interaction databases
FunCoupENSG00000233365
BioGRIDLOC101929297
STRING (EMBL)LOC101929297
ZODIACLOC101929297
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929297
BioCentury BCIQLOC101929297
ClinGenLOC101929297
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929297
Clinical trialLOC101929297
Miscellaneous
canSAR (ICR)LOC101929297 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929297
EVEXLOC101929297
GoPubMedLOC101929297
iHOPLOC101929297
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Jul 30 14:04:20 CEST 2018

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