Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100505938 (uncharacterized LOC100505938)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100505938
Atlas_Id 66768
Location 7p21.3  [Link to chromosome band 7p21]
Location_base_pair Starts at 8301855 and ends at 8382911 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

DNA/RNA

 


External links

Nomenclature
HGNC (Hugo)-   -
Cards
Entrez_Gene (NCBI)LOC100505938  100505938  uncharacterized LOC100505938
Aliases
GeneCards (Weizmann)LOC100505938
Ensembl hg19 (Hinxton) [Gene_View]  chr7:8301855-8382911 [Contig_View]  LOC100505938 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr7:8301855-8382911 [Contig_View]  LOC100505938 [Vega]
TCGA cBioPortalLOC100505938
AceView (NCBI)LOC100505938
Genatlas (Paris)LOC100505938
WikiGenes100505938
SOURCE (Princeton)LOC100505938
Genetics Home Reference (NIH)LOC100505938
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100505938  -     chr7:8301855-8382911 +  7p21.3   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100505938  -     7p21.3   [Description]    (hg38-Dec_2013)
EnsemblLOC100505938 - 7p21.3 [CytoView hg19]  LOC100505938 - 7p21.3 [CytoView hg38]
Mapping of homologs : NCBILOC100505938 [Mapview hg19]  LOC100505938 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BX374774 HG500001 HG500002 HG500003
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000007 NC_018918 NT_007819 NW_004929329
Consensus coding sequences : CCDS (NCBI)LOC100505938
Cluster EST : UnigeneHs.729535 [ NCBI ]
CGAP (NCI)Hs.729535
Gene ExpressionLOC100505938 [ NCBI-GEO ]   LOC100505938 [ EBI - ARRAY_EXPRESS ]   LOC100505938 [ SEEK ]   LOC100505938 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100505938 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100505938
GTEX Portal (Tissue expression)LOC100505938
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100505938
DMDM Disease mutations100505938
Blocks (Seattle)LOC100505938
Protein Interaction databases
BioGRIDLOC100505938
STRING (EMBL)LOC100505938
ZODIACLOC100505938
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100505938
BioCentury BCIQLOC100505938
ClinGenLOC100505938
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100505938
Clinical trialLOC100505938
Miscellaneous
canSAR (ICR)LOC100505938 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100505938
EVEXLOC100505938
GoPubMedLOC100505938
iHOPLOC100505938
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 Mar 14 12:16:57 CET 2017

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