Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928858 (uncharacterized LOC101928858)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928858
Atlas_Id 67446
Location 5q13.1  [Link to chromosome band 5q13]
Location_base_pair Starts at 67793213 and ends at 67801058 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)LOC101928858  101928858  uncharacterized LOC101928858
Aliases
GeneCards (Weizmann)LOC101928858
Ensembl hg19 (Hinxton)ENSG00000249364 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000249364 [Gene_View]  chr5:67793213-67801058 [Contig_View]  LOC101928858 [Vega]
ICGC DataPortalENSG00000249364
TCGA cBioPortalLOC101928858
AceView (NCBI)LOC101928858
Genatlas (Paris)LOC101928858
WikiGenes101928858
SOURCE (Princeton)LOC101928858
Genetics Home Reference (NIH)LOC101928858
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928858  -     chr5:67793213-67801058 +  5q13.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928858  -     5q13.1   [Description]    (hg19-Feb_2009)
EnsemblLOC101928858 - 5q13.1 [CytoView hg19]  LOC101928858 - 5q13.1 [CytoView hg38]
Mapping of homologs : NCBILOC101928858 [Mapview hg19]  LOC101928858 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AV650456 BC042046 BG565489 CA432586
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928858
Cluster EST : UnigeneHs.707837 [ NCBI ]
CGAP (NCI)Hs.707837
Alternative Splicing GalleryENSG00000249364
Gene ExpressionLOC101928858 [ NCBI-GEO ]   LOC101928858 [ EBI - ARRAY_EXPRESS ]   LOC101928858 [ SEEK ]   LOC101928858 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928858 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928858
GTEX Portal (Tissue expression)LOC101928858
Human Protein AtlasENSG00000249364-LOC101928858 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928858
DMDM Disease mutations101928858
Blocks (Seattle)LOC101928858
Human Protein Atlas [tissue]ENSG00000249364-LOC101928858 [tissue]
Protein Interaction databases
FunCoupENSG00000249364
BioGRIDLOC101928858
STRING (EMBL)LOC101928858
ZODIACLOC101928858
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928858
BioCentury BCIQLOC101928858
ClinGenLOC101928858
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928858
Clinical trialLOC101928858
Miscellaneous
canSAR (ICR)LOC101928858 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928858
EVEXLOC101928858
GoPubMedLOC101928858
iHOPLOC101928858
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 : Mon Nov 20 19:48:02 CET 2017

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