Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927351 (uncharacterized LOC101927351)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927351
Atlas_Id 76558
Location 14q21.2  [Link to chromosome band 14q21]
Location_base_pair Starts at 45232360 and ends at 45252032 bp from pter ( according to hg19-Feb_2009)
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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC101927351  101927351  uncharacterized LOC101927351
Aliases
GeneCards (Weizmann)LOC101927351
Ensembl hg19 (Hinxton) [Gene_View]  chr14:45232360-45252032 [Contig_View]  LOC101927351 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr14:45232360-45252032 [Contig_View]  LOC101927351 [Vega]
TCGA cBioPortalLOC101927351
AceView (NCBI)LOC101927351
Genatlas (Paris)LOC101927351
WikiGenes101927351
SOURCE (Princeton)LOC101927351
Genetics Home Reference (NIH)LOC101927351
Genomic and cartography
GoldenPath hg19 (UCSC)LOC101927351  -     chr14:45232360-45252032 -  14q21.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC101927351  -     14q21.2   [Description]    (hg38-Dec_2013)
EnsemblLOC101927351 - 14q21.2 [CytoView hg19]  LOC101927351 - 14q21.2 [CytoView hg38]
Mapping of homologs : NCBILOC101927351 [Mapview hg19]  LOC101927351 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK123685 HG506142 HG506143 HG506144 HG506145
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000014 NC_018925 NT_026437 NW_004929393
Consensus coding sequences : CCDS (NCBI)LOC101927351
Cluster EST : UnigeneHs.196842 [ NCBI ]
CGAP (NCI)Hs.196842
Gene ExpressionLOC101927351 [ NCBI-GEO ]   LOC101927351 [ EBI - ARRAY_EXPRESS ]   LOC101927351 [ SEEK ]   LOC101927351 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927351 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927351
GTEX Portal (Tissue expression)LOC101927351
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927351
DMDM Disease mutations101927351
Blocks (Seattle)LOC101927351
Protein Interaction databases
BioGRIDLOC101927351
STRING (EMBL)LOC101927351
ZODIACLOC101927351
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927351
BioCentury BCIQLOC101927351
ClinGenLOC101927351
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927351
Clinical trialLOC101927351
Miscellaneous
canSAR (ICR)LOC101927351 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927351
EVEXLOC101927351
GoPubMedLOC101927351
iHOPLOC101927351
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 Mar 14 12:18:26 CET 2017

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