Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100506444 (uncharacterized LOC100506444)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100506444
Atlas_Id 66816
Location 4q12  [Link to chromosome band 4q12]
Location_base_pair Starts at 53695901 and ends at 53734358 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)LOC100506444  100506444  uncharacterized LOC100506444
Aliases
GeneCards (Weizmann)LOC100506444
Ensembl hg19 (Hinxton)ENSG00000249341 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000249341 [Gene_View]  chr4:53695901-53734358 [Contig_View]  LOC100506444 [Vega]
ICGC DataPortalENSG00000249341
TCGA cBioPortalLOC100506444
AceView (NCBI)LOC100506444
Genatlas (Paris)LOC100506444
WikiGenes100506444
SOURCE (Princeton)LOC100506444
Genetics Home Reference (NIH)LOC100506444
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100506444  -     chr4:53695901-53734358 +  4q12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100506444  -     4q12   [Description]    (hg19-Feb_2009)
EnsemblLOC100506444 - 4q12 [CytoView hg19]  LOC100506444 - 4q12 [CytoView hg38]
Mapping of homologs : NCBILOC100506444 [Mapview hg19]  LOC100506444 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK129929
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100506444
Cluster EST : UnigeneHs.636176 [ NCBI ]
CGAP (NCI)Hs.636176
Alternative Splicing GalleryENSG00000249341
Gene ExpressionLOC100506444 [ NCBI-GEO ]   LOC100506444 [ EBI - ARRAY_EXPRESS ]   LOC100506444 [ SEEK ]   LOC100506444 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100506444 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100506444
GTEX Portal (Tissue expression)LOC100506444
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100506444
DMDM Disease mutations100506444
Blocks (Seattle)LOC100506444
Human Protein AtlasENSG00000249341
Protein Interaction databases
FunCoupENSG00000249341
BioGRIDLOC100506444
STRING (EMBL)LOC100506444
ZODIACLOC100506444
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100506444
BioCentury BCIQLOC100506444
ClinGenLOC100506444
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100506444
Clinical trialLOC100506444
Miscellaneous
canSAR (ICR)LOC100506444 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100506444
EVEXLOC100506444
GoPubMedLOC100506444
iHOPLOC100506444
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 : Wed Jun 7 16:02:40 CEST 2017

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