Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

LOC100507537 (uncharacterized LOC100507537)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100507537
Atlas_Id 66919
Location 3q25.2  [Link to chromosome band 3q25]
Location_base_pair Starts at 155290232 and ends at 155293700 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)LOC100507537  100507537  uncharacterized LOC100507537
Aliases
GeneCards (Weizmann)LOC100507537
Ensembl hg19 (Hinxton)ENSG00000240045 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000240045 [Gene_View]  chr3:155290232-155293700 [Contig_View]  LOC100507537 [Vega]
ICGC DataPortalENSG00000240045
TCGA cBioPortalLOC100507537
AceView (NCBI)LOC100507537
Genatlas (Paris)LOC100507537
WikiGenes100507537
SOURCE (Princeton)LOC100507537
Genetics Home Reference (NIH)LOC100507537
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100507537  -     chr3:155290232-155293700 -  3q25.2   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100507537  -     3q25.2   [Description]    (hg19-Feb_2009)
EnsemblLOC100507537 - 3q25.2 [CytoView hg19]  LOC100507537 - 3q25.2 [CytoView hg38]
Mapping of homologs : NCBILOC100507537 [Mapview hg19]  LOC100507537 [Mapview hg38]
OMIM616891   
Gene and transcription
Genbank (Entrez)BC015836
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100507537
Cluster EST : UnigeneHs.518341 [ NCBI ]
CGAP (NCI)Hs.518341
Alternative Splicing GalleryENSG00000240045
Gene ExpressionLOC100507537 [ NCBI-GEO ]   LOC100507537 [ EBI - ARRAY_EXPRESS ]   LOC100507537 [ SEEK ]   LOC100507537 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100507537 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507537
GTEX Portal (Tissue expression)LOC100507537
Human Protein AtlasENSG00000240045-LOC100507537 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100507537
DMDM Disease mutations100507537
Blocks (Seattle)LOC100507537
Human Protein Atlas [tissue]ENSG00000240045-LOC100507537 [tissue]
Protein Interaction databases
FunCoupENSG00000240045
BioGRIDLOC100507537
STRING (EMBL)LOC100507537
ZODIACLOC100507537
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100507537
BioCentury BCIQLOC100507537
ClinGenLOC100507537
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507537
Clinical trialLOC100507537
Miscellaneous
canSAR (ICR)LOC100507537 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100507537
EVEXLOC100507537
GoPubMedLOC100507537
iHOPLOC100507537
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 Nov 21 13:49:07 CET 2017

Home   Genes   Leukemias   Solid Tumors   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.