Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928782 (uncharacterized LOC101928782)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928782
Atlas_Id 67428
Location 7q32.3  [Link to chromosome band 7q32]
Location_base_pair Starts at 131910220 and ends at 131948953 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)LOC101928782  101928782  uncharacterized LOC101928782
Aliases
GeneCards (Weizmann)LOC101928782
Ensembl hg19 (Hinxton)ENSG00000224865 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000224865 [Gene_View]  chr7:131910220-131948953 [Contig_View]  LOC101928782 [Vega]
ICGC DataPortalENSG00000224865
TCGA cBioPortalLOC101928782
AceView (NCBI)LOC101928782
Genatlas (Paris)LOC101928782
WikiGenes101928782
SOURCE (Princeton)LOC101928782
Genetics Home Reference (NIH)LOC101928782
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928782  -     chr7:131910220-131948953 +  7q32.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928782  -     7q32.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101928782 - 7q32.3 [CytoView hg19]  LOC101928782 - 7q32.3 [CytoView hg38]
Mapping of homologs : NCBILOC101928782 [Mapview hg19]  LOC101928782 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK098603
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928782
Cluster EST : UnigeneHs.571369 [ NCBI ]
CGAP (NCI)Hs.571369
Alternative Splicing GalleryENSG00000224865
Gene ExpressionLOC101928782 [ NCBI-GEO ]   LOC101928782 [ EBI - ARRAY_EXPRESS ]   LOC101928782 [ SEEK ]   LOC101928782 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928782 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928782
GTEX Portal (Tissue expression)LOC101928782
Human Protein AtlasENSG00000224865-LOC101928782 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928782
DMDM Disease mutations101928782
Blocks (Seattle)LOC101928782
Human Protein Atlas [tissue]ENSG00000224865-LOC101928782 [tissue]
Protein Interaction databases
FunCoupENSG00000224865
BioGRIDLOC101928782
STRING (EMBL)LOC101928782
ZODIACLOC101928782
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928782
BioCentury BCIQLOC101928782
ClinGenLOC101928782
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928782
Clinical trialLOC101928782
Miscellaneous
canSAR (ICR)LOC101928782 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928782
EVEXLOC101928782
GoPubMedLOC101928782
iHOPLOC101928782
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 : Thu Nov 9 12:04:41 CET 2017

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