Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101926933 (uncharacterized LOC101926933)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101926933
Atlas_Id 67016
Location 14q11.2  [Link to chromosome band 14q11]
Location_base_pair Starts at 22929609 and ends at 22954692 bp from pter ( according to hg38-Dec_2013)

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)LOC101926933  101926933  uncharacterized LOC101926933
Aliases
GeneCards (Weizmann)LOC101926933
Ensembl hg19 (Hinxton)ENSG00000257285 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000257285 [Gene_View]  chr14:22929609-22954692 [Contig_View]  LOC101926933 [Vega]
ICGC DataPortalENSG00000257285
TCGA cBioPortalLOC101926933
AceView (NCBI)LOC101926933
Genatlas (Paris)LOC101926933
WikiGenes101926933
SOURCE (Princeton)LOC101926933
Genetics Home Reference (NIH)LOC101926933
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101926933  -     chr14:22929609-22954692 +  14q11.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101926933  -     14q11.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101926933 - 14q11.2 [CytoView hg19]  LOC101926933 - 14q11.2 [CytoView hg38]
Mapping of homologs : NCBILOC101926933 [Mapview hg19]  LOC101926933 [Mapview hg38]
Gene and transcription
Genbank (Entrez)DA905235
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101926933
Cluster EST : UnigeneHs.727321 [ NCBI ]
CGAP (NCI)Hs.727321
Alternative Splicing GalleryENSG00000257285
Gene ExpressionLOC101926933 [ NCBI-GEO ]   LOC101926933 [ EBI - ARRAY_EXPRESS ]   LOC101926933 [ SEEK ]   LOC101926933 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101926933 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101926933
GTEX Portal (Tissue expression)LOC101926933
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101926933
DMDM Disease mutations101926933
Blocks (Seattle)LOC101926933
Human Protein AtlasENSG00000257285
Protein Interaction databases
FunCoupENSG00000257285
BioGRIDLOC101926933
STRING (EMBL)LOC101926933
ZODIACLOC101926933
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101926933
BioCentury BCIQLOC101926933
ClinGenLOC101926933
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101926933
Clinical trialLOC101926933
Miscellaneous
canSAR (ICR)LOC101926933 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101926933
EVEXLOC101926933
GoPubMedLOC101926933
iHOPLOC101926933
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 Aug 1 16:23:24 CEST 2017

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