Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927178 (uncharacterized LOC101927178)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927178
Atlas_Id 67074
Location 14q13.2  [Link to chromosome band 14q13]
Location_base_pair Starts at 35081081 and ends at 35113130 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)LOC101927178  101927178  uncharacterized LOC101927178
Aliases
GeneCards (Weizmann)LOC101927178
Ensembl hg19 (Hinxton)ENSG00000151327 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000151327 [Gene_View]  chr14:35081081-35113130 [Contig_View]  LOC101927178 [Vega]
ICGC DataPortalENSG00000151327
TCGA cBioPortalLOC101927178
AceView (NCBI)LOC101927178
Genatlas (Paris)LOC101927178
WikiGenes101927178
SOURCE (Princeton)LOC101927178
Genetics Home Reference (NIH)LOC101927178
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927178  -     chr14:35081081-35113130 +  14q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927178  -     14q13.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101927178 - 14q13.2 [CytoView hg19]  LOC101927178 - 14q13.2 [CytoView hg38]
Mapping of homologs : NCBILOC101927178 [Mapview hg19]  LOC101927178 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK128559 CK904250 CK904251
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927178
Cluster EST : UnigeneHs.711576 [ NCBI ]
CGAP (NCI)Hs.711576
Alternative Splicing GalleryENSG00000151327
Gene ExpressionLOC101927178 [ NCBI-GEO ]   LOC101927178 [ EBI - ARRAY_EXPRESS ]   LOC101927178 [ SEEK ]   LOC101927178 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927178 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927178
GTEX Portal (Tissue expression)LOC101927178
Human Protein AtlasENSG00000151327-LOC101927178 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927178
DMDM Disease mutations101927178
Blocks (Seattle)LOC101927178
Human Protein Atlas [tissue]ENSG00000151327-LOC101927178 [tissue]
Protein Interaction databases
FunCoupENSG00000151327
BioGRIDLOC101927178
STRING (EMBL)LOC101927178
ZODIACLOC101927178
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927178
BioCentury BCIQLOC101927178
ClinGenLOC101927178
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927178
Clinical trialLOC101927178
Miscellaneous
canSAR (ICR)LOC101927178 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927178
EVEXLOC101927178
GoPubMedLOC101927178
iHOPLOC101927178
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 13:49:48 CET 2017

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