Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101929718 (uncharacterized LOC101929718)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101929718
Atlas_Id 67622
Location 14q11.2  [Link to chromosome band 14q11]
Location_base_pair Starts at 20995837 and ends at 20999163 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)LOC101929718  101929718  uncharacterized LOC101929718
Aliases
GeneCards (Weizmann)LOC101929718
Ensembl hg19 (Hinxton)ENSG00000258471 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258471 [Gene_View]  chr14:20995837-20999163 [Contig_View]  LOC101929718 [Vega]
ICGC DataPortalENSG00000258471
TCGA cBioPortalLOC101929718
AceView (NCBI)LOC101929718
Genatlas (Paris)LOC101929718
WikiGenes101929718
SOURCE (Princeton)LOC101929718
Genetics Home Reference (NIH)LOC101929718
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101929718  -     chr14:20995837-20999163 -  14q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101929718  -     14q11.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101929718 - 14q11.2 [CytoView hg19]  LOC101929718 - 14q11.2 [CytoView hg38]
Mapping of homologs : NCBILOC101929718 [Mapview hg19]  LOC101929718 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK026285
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101929718
Cluster EST : UnigeneHs.706252 [ NCBI ]
CGAP (NCI)Hs.706252
Alternative Splicing GalleryENSG00000258471
Gene ExpressionLOC101929718 [ NCBI-GEO ]   LOC101929718 [ EBI - ARRAY_EXPRESS ]   LOC101929718 [ SEEK ]   LOC101929718 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101929718 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101929718
GTEX Portal (Tissue expression)LOC101929718
Human Protein AtlasENSG00000258471-LOC101929718 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101929718
DMDM Disease mutations101929718
Blocks (Seattle)LOC101929718
Human Protein Atlas [tissue]ENSG00000258471-LOC101929718 [tissue]
Protein Interaction databases
FunCoupENSG00000258471
BioGRIDLOC101929718
STRING (EMBL)LOC101929718
ZODIACLOC101929718
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101929718
BioCentury BCIQLOC101929718
ClinGenLOC101929718
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101929718
Clinical trialLOC101929718
Miscellaneous
canSAR (ICR)LOC101929718 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101929718
EVEXLOC101929718
GoPubMedLOC101929718
iHOPLOC101929718
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 Nov 21 13:52:25 CET 2017

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