Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927179 (uncharacterized LOC101927179)

Identity

Alias (NCBI)-
HGNC (Hugo) -
LocusID (NCBI) 101927179
Atlas_Id 67075
Location 4p12  [Link to chromosome band 4p12]
Location_base_pair Starts at 47831345 and ends at 47896848 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)LOC101927179  101927179  uncharacterized LOC101927179
Aliases
GeneCards (Weizmann)LOC101927179
Ensembl hg19 (Hinxton)ENSG00000282917 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000282917 [Gene_View]  ENSG00000282917 [Sequence]  chr4:47831345-47896848 [Contig_View]  LOC101927179 [Vega]
ICGC DataPortalENSG00000282917
TCGA cBioPortalLOC101927179
AceView (NCBI)LOC101927179
Genatlas (Paris)LOC101927179
WikiGenes101927179
SOURCE (Princeton)LOC101927179
Genetics Home Reference (NIH)LOC101927179
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927179  -     chr4:47831345-47896848 +  4p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927179  -     4p12   [Description]    (hg19-Feb_2009)
GoldenPathLOC101927179 - 4p12 [CytoView hg19]  LOC101927179 - 4p12 [CytoView hg38]
ImmunoBaseENSG00000282917
genome Data Viewer NCBILOC101927179 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AL599247 BX280044
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927179
Alternative Splicing GalleryENSG00000282917
Gene ExpressionLOC101927179 [ NCBI-GEO ]   LOC101927179 [ EBI - ARRAY_EXPRESS ]   LOC101927179 [ SEEK ]   LOC101927179 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927179 [ Firebrowse - Broad ]
GenevisibleExpression of LOC101927179 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)101927179
GTEX Portal (Tissue expression)LOC101927179
Human Protein AtlasENSG00000282917-LOC101927179 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927179
DMDM Disease mutations101927179
Blocks (Seattle)LOC101927179
Human Protein Atlas [tissue]ENSG00000282917-LOC101927179 [tissue]
Protein Interaction databases
FunCoupENSG00000282917
BioGRIDLOC101927179
STRING (EMBL)LOC101927179
ZODIACLOC101927179
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927179
BioCentury BCIQLOC101927179
ClinGenLOC101927179
Clinical trials, drugs, therapy
Protein Interactions : CTD101927179
Clinical trialLOC101927179
Miscellaneous
canSAR (ICR)LOC101927179 (select the gene name)
HarmonizomeLOC101927179
DataMed IndexLOC101927179
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927179
EVEXLOC101927179
GoPubMedLOC101927179
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 : Sat Aug 22 19:20:35 CEST 2020

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