Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927690 (uncharacterized LOC101927690)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927690
Atlas_Id 77618
Location 14q22.3  [Link to chromosome band 14q22]
Location_base_pair Starts at 56514331 and ends at 56551309 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)LOC101927690  101927690  uncharacterized LOC101927690
Aliases
GeneCards (Weizmann)LOC101927690
Ensembl hg19 (Hinxton)ENSG00000258803 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000258803 [Gene_View]  chr14:56514331-56551309 [Contig_View]  LOC101927690 [Vega]
ICGC DataPortalENSG00000258803
TCGA cBioPortalLOC101927690
AceView (NCBI)LOC101927690
Genatlas (Paris)LOC101927690
WikiGenes101927690
SOURCE (Princeton)LOC101927690
Genetics Home Reference (NIH)LOC101927690
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927690  -     chr14:56514331-56551309 +  14q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927690  -     14q22.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101927690 - 14q22.3 [CytoView hg19]  LOC101927690 - 14q22.3 [CytoView hg38]
Mapping of homologs : NCBILOC101927690 [Mapview hg19]  LOC101927690 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC037850 DA296388
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927690
Cluster EST : UnigeneHs.385477 [ NCBI ]
CGAP (NCI)Hs.385477
Alternative Splicing GalleryENSG00000258803
Gene ExpressionLOC101927690 [ NCBI-GEO ]   LOC101927690 [ EBI - ARRAY_EXPRESS ]   LOC101927690 [ SEEK ]   LOC101927690 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927690 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927690
GTEX Portal (Tissue expression)LOC101927690
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927690
DMDM Disease mutations101927690
Blocks (Seattle)LOC101927690
Human Protein AtlasENSG00000258803
Protein Interaction databases
FunCoupENSG00000258803
BioGRIDLOC101927690
STRING (EMBL)LOC101927690
ZODIACLOC101927690
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927690
BioCentury BCIQLOC101927690
ClinGenLOC101927690
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927690
Clinical trialLOC101927690
Miscellaneous
canSAR (ICR)LOC101927690 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927690
EVEXLOC101927690
GoPubMedLOC101927690
iHOPLOC101927690
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 : Fri May 19 11:28:27 CEST 2017

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