Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100507437 (uncharacterized LOC100507437)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100507437
Atlas_Id 66904
Location 14q32.33  [Link to chromosome band 14q32]
Location_base_pair Starts at 105417581 and ends at 105419739 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)LOC100507437  100507437  uncharacterized LOC100507437
Aliases
GeneCards (Weizmann)LOC100507437
Ensembl hg19 (Hinxton)ENSG00000251602 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000251602 [Gene_View]  chr14:105417581-105419739 [Contig_View]  LOC100507437 [Vega]
ICGC DataPortalENSG00000251602
TCGA cBioPortalLOC100507437
AceView (NCBI)LOC100507437
Genatlas (Paris)LOC100507437
WikiGenes100507437
SOURCE (Princeton)LOC100507437
Genetics Home Reference (NIH)LOC100507437
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100507437  -     chr14:105417581-105419739 -  14q32.33   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100507437  -     14q32.33   [Description]    (hg19-Feb_2009)
EnsemblLOC100507437 - 14q32.33 [CytoView hg19]  LOC100507437 - 14q32.33 [CytoView hg38]
Mapping of homologs : NCBILOC100507437 [Mapview hg19]  LOC100507437 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK123017 BU850282
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100507437
Cluster EST : UnigeneHs.676548 [ NCBI ]
CGAP (NCI)Hs.676548
Alternative Splicing GalleryENSG00000251602
Gene ExpressionLOC100507437 [ NCBI-GEO ]   LOC100507437 [ EBI - ARRAY_EXPRESS ]   LOC100507437 [ SEEK ]   LOC100507437 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100507437 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100507437
GTEX Portal (Tissue expression)LOC100507437
Human Protein AtlasENSG00000251602-LOC100507437 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100507437
DMDM Disease mutations100507437
Blocks (Seattle)LOC100507437
Human Protein Atlas [tissue]ENSG00000251602-LOC100507437 [tissue]
Protein Interaction databases
FunCoupENSG00000251602
BioGRIDLOC100507437
STRING (EMBL)LOC100507437
ZODIACLOC100507437
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100507437
BioCentury BCIQLOC100507437
ClinGenLOC100507437
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100507437
Clinical trialLOC100507437
Miscellaneous
canSAR (ICR)LOC100507437 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100507437
EVEXLOC100507437
GoPubMedLOC100507437
iHOPLOC100507437
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 Nov 21 13:49:04 CET 2017

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