Atlas of Genetics and Cytogenetics in Oncology and Haematology

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LOC101927884 (uncharacterized LOC101927884)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927884
Atlas_Id 67241
Location 2p12  [Link to chromosome band 2p12]
Location_base_pair Starts at 75524068 and ends at 75542706 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)LOC101927884  101927884  uncharacterized LOC101927884
Aliases
GeneCards (Weizmann)LOC101927884
Ensembl hg19 (Hinxton)ENSG00000231172 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000231172 [Gene_View]  ENSG00000231172 [Sequence]  chr2:75524068-75542706 [Contig_View]  LOC101927884 [Vega]
ICGC DataPortalENSG00000231172
TCGA cBioPortalLOC101927884
AceView (NCBI)LOC101927884
Genatlas (Paris)LOC101927884
WikiGenes101927884
SOURCE (Princeton)LOC101927884
Genetics Home Reference (NIH)LOC101927884
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927884  -     chr2:75524068-75542706 +  2p12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927884  -     2p12   [Description]    (hg19-Feb_2009)
GoldenPathLOC101927884 - 2p12 [CytoView hg19]  LOC101927884 - 2p12 [CytoView hg38]
ImmunoBaseENSG00000231172
genome Data Viewer NCBILOC101927884 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)BC018659
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927884
Alternative Splicing GalleryENSG00000231172
Gene ExpressionLOC101927884 [ NCBI-GEO ]   LOC101927884 [ EBI - ARRAY_EXPRESS ]   LOC101927884 [ SEEK ]   LOC101927884 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927884 [ Firebrowse - Broad ]
GenevisibleExpression of LOC101927884 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)101927884
GTEX Portal (Tissue expression)LOC101927884
Human Protein AtlasENSG00000231172-LOC101927884 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927884
DMDM Disease mutations101927884
Blocks (Seattle)LOC101927884
Human Protein Atlas [tissue]ENSG00000231172-LOC101927884 [tissue]
Protein Interaction databases
FunCoupENSG00000231172
BioGRIDLOC101927884
STRING (EMBL)LOC101927884
ZODIACLOC101927884
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927884
BioCentury BCIQLOC101927884
ClinGenLOC101927884
Clinical trials, drugs, therapy
Protein Interactions : CTD101927884
Clinical trialLOC101927884
Miscellaneous
canSAR (ICR)LOC101927884 (select the gene name)
HarmonizomeLOC101927884
DataMed IndexLOC101927884
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927884
EVEXLOC101927884
GoPubMedLOC101927884
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Fri Jul 10 20:16:28 CEST 2020
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