Atlas of Genetics and Cytogenetics in Oncology and Haematology

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LOC101927762 (uncharacterized LOC101927762)


Alias (NCBI)-
HGNC (Hugo) -
LocusID (NCBI) 101927762
Atlas_Id 67207
Location 10p15.3  [Link to chromosome band 10p15]
Location_base_pair Starts at 933026 and ends at 942743 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)


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

HGNC (Hugo)-   -
Entrez_Gene (NCBI)LOC101927762    uncharacterized LOC101927762
GeneCards (Weizmann)LOC101927762
Ensembl hg19 (Hinxton)ENSG00000229869 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000229869 [Gene_View]  ENSG00000229869 [Sequence]  chr10:933026-942743 [Contig_View]  LOC101927762 [Vega]
ICGC DataPortalENSG00000229869
TCGA cBioPortalLOC101927762
AceView (NCBI)LOC101927762
Genatlas (Paris)LOC101927762
SOURCE (Princeton)LOC101927762
Genetics Home Reference (NIH)LOC101927762
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927762  -     chr10:933026-942743 +  10p15.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927762  -     10p15.3   [Description]    (hg19-Feb_2009)
GoldenPathLOC101927762 - 10p15.3 [CytoView hg19]  LOC101927762 - 10p15.3 [CytoView hg38]
Genome Data Viewer NCBILOC101927762 [Mapview hg19]  
Gene and transcription
Genbank (Entrez)AI989559 OA985662
RefSeq transcript (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927762
Gene ExpressionLOC101927762 [ NCBI-GEO ]   LOC101927762 [ EBI - ARRAY_EXPRESS ]   LOC101927762 [ SEEK ]   LOC101927762 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927762 [ Firebrowse - Broad ]
GenevisibleExpression of LOC101927762 in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)101927762
GTEX Portal (Tissue expression)LOC101927762
Human Protein AtlasENSG00000229869-LOC101927762 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927762
Human Protein Atlas [tissue]ENSG00000229869-LOC101927762 [tissue]
Protein Interaction databases
Ontologies - Pathways
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Oct 4 16:02:28 CEST 2021

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