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LOC100130597 (uncharacterized LOC100130597)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100130597
Atlas_Id 66412
Location 21q22.3  [Link to chromosome band 21q22]
Location_base_pair Starts at 46953347 and ends at 46955696 bp from pter ( according to hg19-Feb_2009)
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


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100130597  100130597  uncharacterized LOC100130597
Aliases
GeneCards (Weizmann)LOC100130597
Ensembl hg19 (Hinxton) [Gene_View]  chr21:46953347-46955696 [Contig_View]  LOC100130597 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr21:46953347-46955696 [Contig_View]  LOC100130597 [Vega]
TCGA cBioPortalLOC100130597
AceView (NCBI)LOC100130597
Genatlas (Paris)LOC100130597
WikiGenes100130597
SOURCE (Princeton)LOC100130597
Genetics Home Reference (NIH)LOC100130597
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100130597  -     chr21:46953347-46955696 -  21q22.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100130597  -     21q22.3   [Description]    (hg38-Dec_2013)
EnsemblLOC100130597 - 21q22.3 [CytoView hg19]  LOC100130597 - 21q22.3 [CytoView hg38]
Mapping of homologs : NCBILOC100130597 [Mapview hg19]  LOC100130597 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK127669
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)AC_000153 NC_000021 NT_011515 NW_001838716
Consensus coding sequences : CCDS (NCBI)LOC100130597
Cluster EST : UnigeneHs.84190 [ NCBI ]
CGAP (NCI)Hs.84190
Gene ExpressionLOC100130597 [ NCBI-GEO ]   LOC100130597 [ EBI - ARRAY_EXPRESS ]   LOC100130597 [ SEEK ]   LOC100130597 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100130597 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100130597
GTEX Portal (Tissue expression)LOC100130597
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100130597
DMDM Disease mutations100130597
Blocks (Seattle)LOC100130597
IPIIPI00883895   
Protein Interaction databases
BioGRIDLOC100130597
STRING (EMBL)LOC100130597
ZODIACLOC100130597
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100130597
BioCentury BCIQLOC100130597
ClinGenLOC100130597
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100130597
Clinical trialLOC100130597
Miscellaneous
canSAR (ICR)LOC100130597 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100130597
EVEXLOC100130597
GoPubMedLOC100130597
iHOPLOC100130597
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 12:15:36 CET 2017

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