Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC101928565 (uncharacterized LOC101928565)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 101928565
Atlas_Id 67387
Location 1q24.2  [Link to chromosome band 1q24]
Location_base_pair Starts at 168464114 and ends at 168495644 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)LOC101928565  101928565  uncharacterized LOC101928565
Aliases
GeneCards (Weizmann)LOC101928565
Ensembl hg19 (Hinxton)ENSG00000237658 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000237658 [Gene_View]  chr1:168464114-168495644 [Contig_View]  LOC101928565 [Vega]
ICGC DataPortalENSG00000237658
TCGA cBioPortalLOC101928565
AceView (NCBI)LOC101928565
Genatlas (Paris)LOC101928565
WikiGenes101928565
SOURCE (Princeton)LOC101928565
Genetics Home Reference (NIH)LOC101928565
Genomic and cartography
GoldenPath hg38 (UCSC)LOC101928565  -     chr1:168464114-168495644 -  1q24.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC101928565  -     1q24.2   [Description]    (hg19-Feb_2009)
EnsemblLOC101928565 - 1q24.2 [CytoView hg19]  LOC101928565 - 1q24.2 [CytoView hg38]
Mapping of homologs : NCBILOC101928565 [Mapview hg19]  LOC101928565 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF085892 AF087964
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC101928565
Cluster EST : UnigeneHs.638741 [ NCBI ]
CGAP (NCI)Hs.638741
Alternative Splicing GalleryENSG00000237658
Gene ExpressionLOC101928565 [ NCBI-GEO ]   LOC101928565 [ EBI - ARRAY_EXPRESS ]   LOC101928565 [ SEEK ]   LOC101928565 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC101928565 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)101928565
GTEX Portal (Tissue expression)LOC101928565
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC101928565
DMDM Disease mutations101928565
Blocks (Seattle)LOC101928565
Human Protein AtlasENSG00000237658
Protein Interaction databases
FunCoupENSG00000237658
BioGRIDLOC101928565
STRING (EMBL)LOC101928565
ZODIACLOC101928565
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease101928565
BioCentury BCIQLOC101928565
ClinGenLOC101928565
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD101928565
Clinical trialLOC101928565
Miscellaneous
canSAR (ICR)LOC101928565 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC101928565
EVEXLOC101928565
GoPubMedLOC101928565
iHOPLOC101928565
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 : Mon Sep 18 13:20:59 CEST 2017

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