Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101930114 (uncharacterized LOC101930114)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101930114
Atlas_Id 78111
Location 1q32.2  [Link to chromosome band 1q32]
Location_base_pair Starts at 209661359 and ends at 209724125 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)LOC101930114  101930114  uncharacterized LOC101930114
Aliases
GeneCards (Weizmann)LOC101930114
Ensembl hg19 (Hinxton)ENSG00000227591 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000227591 [Gene_View]  chr1:209661359-209724125 [Contig_View]  LOC101930114 [Vega]
ICGC DataPortalENSG00000227591
TCGA cBioPortalLOC101930114
AceView (NCBI)LOC101930114
Genatlas (Paris)LOC101930114
WikiGenes101930114
SOURCE (Princeton)LOC101930114
Genetics Home Reference (NIH)LOC101930114
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101930114  -     chr1:209661359-209724125 -  1q32.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101930114  -     1q32.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101930114 - 1q32.2 [CytoView hg19]  LOC101930114 - 1q32.2 [CytoView hg38]
Mapping of homologs : NCBILOC101930114 [Mapview hg19]  LOC101930114 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA601997 AI928031 AI984837 BM929336
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101930114
Cluster EST : UnigeneHs.663934 [ NCBI ]
CGAP (NCI)Hs.663934
Alternative Splicing GalleryENSG00000227591
Gene ExpressionLOC101930114 [ NCBI-GEO ]   LOC101930114 [ EBI - ARRAY_EXPRESS ]   LOC101930114 [ SEEK ]   LOC101930114 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101930114 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101930114
GTEX Portal (Tissue expression)LOC101930114
Human Protein AtlasENSG00000227591-LOC101930114 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101930114
DMDM Disease mutations101930114
Blocks (Seattle)LOC101930114
Human Protein Atlas [tissue]ENSG00000227591-LOC101930114 [tissue]
Protein Interaction databases
FunCoupENSG00000227591
BioGRIDLOC101930114
STRING (EMBL)LOC101930114
ZODIACLOC101930114
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101930114
BioCentury BCIQLOC101930114
ClinGenLOC101930114
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101930114
Clinical trialLOC101930114
Miscellaneous
canSAR (ICR)LOC101930114 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101930114
EVEXLOC101930114
GoPubMedLOC101930114
iHOPLOC101930114
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 Nov 20 19:49:00 CET 2017

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