Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929006 (uncharacterized LOC101929006)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929006
Atlas_Id 78079
Location 6p22.1  [Link to chromosome band 6p22]
Location_base_pair Starts at 29223973 and ends at 29267085 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)LOC101929006  101929006  uncharacterized LOC101929006
Aliases
GeneCards (Weizmann)LOC101929006
Ensembl hg19 (Hinxton)ENSG00000232505 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000232505 [Gene_View]  ENSG00000232505 [Sequence]  chr6:29223973-29267085 [Contig_View]  LOC101929006 [Vega]
ICGC DataPortalENSG00000232505
TCGA cBioPortalLOC101929006
AceView (NCBI)LOC101929006
Genatlas (Paris)LOC101929006
WikiGenes101929006
SOURCE (Princeton)LOC101929006
Genetics Home Reference (NIH)LOC101929006
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929006  -     chr6:29223973-29267085 +  6p22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929006  -     6p22.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101929006 - 6p22.1 [CytoView hg19]  LOC101929006 - 6p22.1 [CytoView hg38]
Mapping of homologs : NCBILOC101929006 [Mapview hg19]  LOC101929006 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI184585 AW072314 BX100796
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000006 NC_018917 NT_113891 NT_167244 NT_167245 NT_167246 NT_167247 NT_167249
Consensus coding sequences : CCDS (NCBI)LOC101929006
Cluster EST : UnigeneHs.132477 [ NCBI ]
CGAP (NCI)Hs.132477
Alternative Splicing GalleryENSG00000232505
Gene ExpressionLOC101929006 [ NCBI-GEO ]   LOC101929006 [ EBI - ARRAY_EXPRESS ]   LOC101929006 [ SEEK ]   LOC101929006 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929006 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929006
GTEX Portal (Tissue expression)LOC101929006
Human Protein AtlasENSG00000232505-LOC101929006 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929006
DMDM Disease mutations101929006
Blocks (Seattle)LOC101929006
Human Protein Atlas [tissue]ENSG00000232505-LOC101929006 [tissue]
Protein Interaction databases
FunCoupENSG00000232505
BioGRIDLOC101929006
STRING (EMBL)LOC101929006
ZODIACLOC101929006
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929006
BioCentury BCIQLOC101929006
ClinGenLOC101929006
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929006
Clinical trialLOC101929006
Miscellaneous
canSAR (ICR)LOC101929006 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929006
EVEXLOC101929006
GoPubMedLOC101929006
iHOPLOC101929006
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 14:04:03 CEST 2018

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