Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928820 (uncharacterized LOC101928820)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928820
Atlas_Id 76922
Location 6q14.3  [Link to chromosome band 6q14]
Location_base_pair Starts at 85387219 and ends at 85404802 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)LOC101928820  101928820  uncharacterized LOC101928820
Aliases
GeneCards (Weizmann)LOC101928820
Ensembl hg19 (Hinxton)ENSG00000234155 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000234155 [Gene_View]  ENSG00000234155 [Sequence]  chr6:85387219-85404802 [Contig_View]  LOC101928820 [Vega]
ICGC DataPortalENSG00000234155
TCGA cBioPortalLOC101928820
AceView (NCBI)LOC101928820
Genatlas (Paris)LOC101928820
WikiGenes101928820
SOURCE (Princeton)LOC101928820
Genetics Home Reference (NIH)LOC101928820
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928820  -     chr6:85387219-85404802 -  6q14.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928820  -     6q14.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101928820 - 6q14.3 [CytoView hg19]  LOC101928820 - 6q14.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928820 [Mapview hg19]  LOC101928820 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB371547 AK024998
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928820
Cluster EST : UnigeneHs.738392 [ NCBI ]
CGAP (NCI)Hs.738392
Alternative Splicing GalleryENSG00000234155
Gene ExpressionLOC101928820 [ NCBI-GEO ]   LOC101928820 [ EBI - ARRAY_EXPRESS ]   LOC101928820 [ SEEK ]   LOC101928820 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928820 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928820
GTEX Portal (Tissue expression)LOC101928820
Human Protein AtlasENSG00000234155-LOC101928820 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928820
DMDM Disease mutations101928820
Blocks (Seattle)LOC101928820
Human Protein Atlas [tissue]ENSG00000234155-LOC101928820 [tissue]
Protein Interaction databases
FunCoupENSG00000234155
BioGRIDLOC101928820
STRING (EMBL)LOC101928820
ZODIACLOC101928820
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928820
BioCentury BCIQLOC101928820
ClinGenLOC101928820
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928820
Clinical trialLOC101928820
Miscellaneous
canSAR (ICR)LOC101928820 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928820
EVEXLOC101928820
GoPubMedLOC101928820
iHOPLOC101928820
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Jul 30 14:03:51 CEST 2018

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