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LOC101928942 (uncharacterized LOC101928942)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928942
Atlas_Id 67464
Location 4q21.21  [Link to chromosome band 4q21]
Location_base_pair Starts at 81164940 and ends at 81193395 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)LOC101928942  101928942  uncharacterized LOC101928942
Aliases
GeneCards (Weizmann)LOC101928942
Ensembl hg19 (Hinxton)ENSG00000251059 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000251059 [Gene_View]  chr4:81164940-81193395 [Contig_View]  LOC101928942 [Vega]
ICGC DataPortalENSG00000251059
TCGA cBioPortalLOC101928942
AceView (NCBI)LOC101928942
Genatlas (Paris)LOC101928942
WikiGenes101928942
SOURCE (Princeton)LOC101928942
Genetics Home Reference (NIH)LOC101928942
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928942  -     chr4:81164940-81193395 +  4q21.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928942  -     4q21.21   [Description]    (hg19-Feb_2009)
EnsemblLOC101928942 - 4q21.21 [CytoView hg19]  LOC101928942 - 4q21.21 [CytoView hg38]
Mapping of homologs : NCBILOC101928942 [Mapview hg19]  LOC101928942 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AW085934 BX097499
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928942
Cluster EST : UnigeneHs.664002 [ NCBI ]
CGAP (NCI)Hs.664002
Alternative Splicing GalleryENSG00000251059
Gene ExpressionLOC101928942 [ NCBI-GEO ]   LOC101928942 [ EBI - ARRAY_EXPRESS ]   LOC101928942 [ SEEK ]   LOC101928942 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928942 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928942
GTEX Portal (Tissue expression)LOC101928942
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928942
DMDM Disease mutations101928942
Blocks (Seattle)LOC101928942
Human Protein AtlasENSG00000251059
Protein Interaction databases
FunCoupENSG00000251059
BioGRIDLOC101928942
STRING (EMBL)LOC101928942
ZODIACLOC101928942
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928942
BioCentury BCIQLOC101928942
ClinGenLOC101928942
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928942
Clinical trialLOC101928942
Miscellaneous
canSAR (ICR)LOC101928942 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928942
EVEXLOC101928942
GoPubMedLOC101928942
iHOPLOC101928942
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 : Tue Aug 1 16:24:46 CEST 2017

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