Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101927787 (uncharacterized LOC101927787)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101927787
Atlas_Id 67214
Location 1q42.3  [Link to chromosome band 1q42]
Location_base_pair Starts at 234646289 and ends at 234660924 bp from pter ( according to hg38-Dec_2013)

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)LOC101927787  101927787  uncharacterized LOC101927787
Aliases
GeneCards (Weizmann)LOC101927787
Ensembl hg19 (Hinxton)ENSG00000228044 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000228044 [Gene_View]  chr1:234646289-234660924 [Contig_View]  LOC101927787 [Vega]
ICGC DataPortalENSG00000228044
TCGA cBioPortalLOC101927787
AceView (NCBI)LOC101927787
Genatlas (Paris)LOC101927787
WikiGenes101927787
SOURCE (Princeton)LOC101927787
Genetics Home Reference (NIH)LOC101927787
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101927787  -     chr1:234646289-234660924 +  1q42.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101927787  -     1q42.3   [Description]    (hg19-Feb_2009)
EnsemblLOC101927787 - 1q42.3 [CytoView hg19]  LOC101927787 - 1q42.3 [CytoView hg38]
Mapping of homologs : NCBILOC101927787 [Mapview hg19]  LOC101927787 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC032040
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101927787
Cluster EST : UnigeneHs.520658 [ NCBI ]
CGAP (NCI)Hs.520658
Alternative Splicing GalleryENSG00000228044
Gene ExpressionLOC101927787 [ NCBI-GEO ]   LOC101927787 [ EBI - ARRAY_EXPRESS ]   LOC101927787 [ SEEK ]   LOC101927787 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101927787 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101927787
GTEX Portal (Tissue expression)LOC101927787
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101927787
DMDM Disease mutations101927787
Blocks (Seattle)LOC101927787
Human Protein AtlasENSG00000228044
Protein Interaction databases
FunCoupENSG00000228044
BioGRIDLOC101927787
STRING (EMBL)LOC101927787
ZODIACLOC101927787
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101927787
BioCentury BCIQLOC101927787
ClinGenLOC101927787
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101927787
Clinical trialLOC101927787
Miscellaneous
canSAR (ICR)LOC101927787 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101927787
EVEXLOC101927787
GoPubMedLOC101927787
iHOPLOC101927787
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 : Wed Jun 7 16:04:33 CEST 2017

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