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LOC100506175 (uncharacterized LOC100506175)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506175
Atlas_Id 66789
Location 20q13.13  [Link to chromosome band 20q13]
Location_base_pair Starts at 50645471 and ends at 50660291 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)LOC100506175  100506175  uncharacterized LOC100506175
Aliases
GeneCards (Weizmann)LOC100506175
Ensembl hg19 (Hinxton)ENSG00000234693 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000234693 [Gene_View]  chr20:50645471-50660291 [Contig_View]  LOC100506175 [Vega]
ICGC DataPortalENSG00000234693
TCGA cBioPortalLOC100506175
AceView (NCBI)LOC100506175
Genatlas (Paris)LOC100506175
WikiGenes100506175
SOURCE (Princeton)LOC100506175
Genetics Home Reference (NIH)LOC100506175
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506175  -     chr20:50645471-50660291 +  20q13.13   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506175  -     20q13.13   [Description]    (hg19-Feb_2009)
EnsemblLOC100506175 - 20q13.13 [CytoView hg19]  LOC100506175 - 20q13.13 [CytoView hg38]
Mapping of homologs : NCBILOC100506175 [Mapview hg19]  LOC100506175 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA044156 CF130631
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506175
Cluster EST : UnigeneHs.658270 [ NCBI ]
CGAP (NCI)Hs.658270
Alternative Splicing GalleryENSG00000234693
Gene ExpressionLOC100506175 [ NCBI-GEO ]   LOC100506175 [ EBI - ARRAY_EXPRESS ]   LOC100506175 [ SEEK ]   LOC100506175 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506175 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506175
GTEX Portal (Tissue expression)LOC100506175
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506175
DMDM Disease mutations100506175
Blocks (Seattle)LOC100506175
Human Protein AtlasENSG00000234693
Protein Interaction databases
FunCoupENSG00000234693
BioGRIDLOC100506175
STRING (EMBL)LOC100506175
ZODIACLOC100506175
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506175
BioCentury BCIQLOC100506175
ClinGenLOC100506175
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506175
Clinical trialLOC100506175
Miscellaneous
canSAR (ICR)LOC100506175 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506175
EVEXLOC100506175
GoPubMedLOC100506175
iHOPLOC100506175
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 13:18:47 CEST 2017

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