Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100287704 (uncharacterized LOC100287704)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100287704
Atlas_Id 66645
Location 7q11.21  [Link to chromosome band 7q11]
Location_base_pair Starts at 63348861 and ends at 63351773 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)LOC100287704  100287704  uncharacterized LOC100287704
Aliases
GeneCards (Weizmann)LOC100287704
Ensembl hg19 (Hinxton)ENSG00000230000 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000230000 [Gene_View]  chr7:63348861-63351773 [Contig_View]  LOC100287704 [Vega]
ICGC DataPortalENSG00000230000
TCGA cBioPortalLOC100287704
AceView (NCBI)LOC100287704
Genatlas (Paris)LOC100287704
WikiGenes100287704
SOURCE (Princeton)LOC100287704
Genetics Home Reference (NIH)LOC100287704
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100287704  -     chr7:63348861-63351773 +  7q11.21   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100287704  -     7q11.21   [Description]    (hg19-Feb_2009)
EnsemblLOC100287704 - 7q11.21 [CytoView hg19]  LOC100287704 - 7q11.21 [CytoView hg38]
Mapping of homologs : NCBILOC100287704 [Mapview hg19]  LOC100287704 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK128835 BC040831
RefSeq transcript (Entrez)NM_001013684
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100287704
Cluster EST : UnigeneHs.740703 [ NCBI ]
CGAP (NCI)Hs.740703
Alternative Splicing GalleryENSG00000230000
Gene ExpressionLOC100287704 [ NCBI-GEO ]   LOC100287704 [ EBI - ARRAY_EXPRESS ]   LOC100287704 [ SEEK ]   LOC100287704 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100287704 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100287704
GTEX Portal (Tissue expression)LOC100287704
Human Protein AtlasENSG00000230000-LOC100287704 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100287704
DMDM Disease mutations100287704
Blocks (Seattle)LOC100287704
Human Protein Atlas [tissue]ENSG00000230000-LOC100287704 [tissue]
IPIIPI00418705   
Protein Interaction databases
FunCoupENSG00000230000
BioGRIDLOC100287704
STRING (EMBL)LOC100287704
ZODIACLOC100287704
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100287704
BioCentury BCIQLOC100287704
ClinGenLOC100287704
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100287704
Clinical trialLOC100287704
Miscellaneous
canSAR (ICR)LOC100287704 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100287704
EVEXLOC100287704
GoPubMedLOC100287704
iHOPLOC100287704
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 : Thu Nov 9 12:01:15 CET 2017

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