Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100508631 (uncharacterized LOC100508631)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100508631
Atlas_Id 77236
Location 4p14  [Link to chromosome band 4p14]
Location_base_pair Starts at 37001779 and ends at 37020706 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)LOC100508631  100508631  uncharacterized LOC100508631
Aliases
GeneCards (Weizmann)LOC100508631
Ensembl hg19 (Hinxton)ENSG00000261761 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000261761 [Gene_View]  chr4:37001779-37020706 [Contig_View]  LOC100508631 [Vega]
ICGC DataPortalENSG00000261761
TCGA cBioPortalLOC100508631
AceView (NCBI)LOC100508631
Genatlas (Paris)LOC100508631
WikiGenes100508631
SOURCE (Princeton)LOC100508631
Genetics Home Reference (NIH)LOC100508631
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100508631  -     chr4:37001779-37020706 +  4p14   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100508631  -     4p14   [Description]    (hg19-Feb_2009)
EnsemblLOC100508631 - 4p14 [CytoView hg19]  LOC100508631 - 4p14 [CytoView hg38]
Mapping of homologs : NCBILOC100508631 [Mapview hg19]  LOC100508631 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BC042993 BG621125 BU568933 BU620996
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100508631
Cluster EST : UnigeneHs.737759 [ NCBI ]
CGAP (NCI)Hs.737759
Alternative Splicing GalleryENSG00000261761
Gene ExpressionLOC100508631 [ NCBI-GEO ]   LOC100508631 [ EBI - ARRAY_EXPRESS ]   LOC100508631 [ SEEK ]   LOC100508631 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100508631 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100508631
GTEX Portal (Tissue expression)LOC100508631
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100508631
DMDM Disease mutations100508631
Blocks (Seattle)LOC100508631
Human Protein AtlasENSG00000261761
Protein Interaction databases
FunCoupENSG00000261761
BioGRIDLOC100508631
STRING (EMBL)LOC100508631
ZODIACLOC100508631
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100508631
BioCentury BCIQLOC100508631
ClinGenLOC100508631
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100508631
Clinical trialLOC100508631
Miscellaneous
canSAR (ICR)LOC100508631 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100508631
EVEXLOC100508631
GoPubMedLOC100508631
iHOPLOC100508631
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 16:03:12 CEST 2017

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