Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927356 (uncharacterized LOC101927356)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927356
Atlas_Id 67117
Location 7q21.11  [Link to chromosome band 7q21]
Location_base_pair Starts at 82009177 and ends at 82029955 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)LOC101927356  101927356  uncharacterized LOC101927356
Aliases
GeneCards (Weizmann)LOC101927356
Ensembl hg19 (Hinxton)ENSG00000223770 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000223770 [Gene_View]  chr7:82009177-82029955 [Contig_View]  LOC101927356 [Vega]
ICGC DataPortalENSG00000223770
TCGA cBioPortalLOC101927356
AceView (NCBI)LOC101927356
Genatlas (Paris)LOC101927356
WikiGenes101927356
SOURCE (Princeton)LOC101927356
Genetics Home Reference (NIH)LOC101927356
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927356  -     chr7:82009177-82029955 +  7q21.11   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927356  -     7q21.11   [Description]    (hg19-Feb_2009)
EnsemblLOC101927356 - 7q21.11 [CytoView hg19]  LOC101927356 - 7q21.11 [CytoView hg38]
Mapping of homologs : NCBILOC101927356 [Mapview hg19]  LOC101927356 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK055932 BM468380
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927356
Cluster EST : UnigeneHs.571348 [ NCBI ]
CGAP (NCI)Hs.571348
Alternative Splicing GalleryENSG00000223770
Gene ExpressionLOC101927356 [ NCBI-GEO ]   LOC101927356 [ EBI - ARRAY_EXPRESS ]   LOC101927356 [ SEEK ]   LOC101927356 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927356 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927356
GTEX Portal (Tissue expression)LOC101927356
Human Protein AtlasENSG00000223770-LOC101927356 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927356
DMDM Disease mutations101927356
Blocks (Seattle)LOC101927356
Human Protein Atlas [tissue]ENSG00000223770-LOC101927356 [tissue]
Protein Interaction databases
FunCoupENSG00000223770
BioGRIDLOC101927356
STRING (EMBL)LOC101927356
ZODIACLOC101927356
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927356
BioCentury BCIQLOC101927356
ClinGenLOC101927356
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927356
Clinical trialLOC101927356
Miscellaneous
canSAR (ICR)LOC101927356 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927356
EVEXLOC101927356
GoPubMedLOC101927356
iHOPLOC101927356
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 : Thu Nov 9 12:03:10 CET 2017

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