Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100505622 (uncharacterized LOC100505622)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100505622
Atlas_Id 66743
Location 19q13.2  [Link to chromosome band 19q13]
Location_base_pair Starts at 42132629 and ends at 42137099 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)LOC100505622  100505622  uncharacterized LOC100505622
Aliases
GeneCards (Weizmann)LOC100505622
Ensembl hg19 (Hinxton)ENSG00000254887 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000254887 [Gene_View]  chr19:42132629-42137099 [Contig_View]  LOC100505622 [Vega]
ICGC DataPortalENSG00000254887
TCGA cBioPortalLOC100505622
AceView (NCBI)LOC100505622
Genatlas (Paris)LOC100505622
WikiGenes100505622
SOURCE (Princeton)LOC100505622
Genetics Home Reference (NIH)LOC100505622
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100505622  -     chr19:42132629-42137099 +  19q13.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100505622  -     19q13.2   [Description]    (hg19-Feb_2009)
EnsemblLOC100505622 - 19q13.2 [CytoView hg19]  LOC100505622 - 19q13.2 [CytoView hg38]
Mapping of homologs : NCBILOC100505622 [Mapview hg19]  LOC100505622 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC015776 BC042152
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100505622
Cluster EST : UnigeneHs.661761 [ NCBI ]
CGAP (NCI)Hs.661761
Alternative Splicing GalleryENSG00000254887
Gene ExpressionLOC100505622 [ NCBI-GEO ]   LOC100505622 [ EBI - ARRAY_EXPRESS ]   LOC100505622 [ SEEK ]   LOC100505622 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100505622 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505622
GTEX Portal (Tissue expression)LOC100505622
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100505622
DMDM Disease mutations100505622
Blocks (Seattle)LOC100505622
Human Protein AtlasENSG00000254887
Protein Interaction databases
FunCoupENSG00000254887
BioGRIDLOC100505622
STRING (EMBL)LOC100505622
ZODIACLOC100505622
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100505622
BioCentury BCIQLOC100505622
ClinGenLOC100505622
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505622
Clinical trialLOC100505622
Miscellaneous
canSAR (ICR)LOC100505622 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100505622
EVEXLOC100505622
GoPubMedLOC100505622
iHOPLOC100505622
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 13:18:38 CEST 2017

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