Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC102723778 (uncharacterized LOC102723778)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 102723778
Atlas_Id 67700
Location 4p15.1  [Link to chromosome band 4p15]
Location_base_pair Starts at 31171144 and ends at 31211674 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)LOC102723778  102723778  uncharacterized LOC102723778
Aliases
GeneCards (Weizmann)LOC102723778
Ensembl hg19 (Hinxton)ENSG00000251182 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000251182 [Gene_View]  chr4:31171144-31211674 [Contig_View]  LOC102723778 [Vega]
ICGC DataPortalENSG00000251182
TCGA cBioPortalLOC102723778
AceView (NCBI)LOC102723778
Genatlas (Paris)LOC102723778
WikiGenes102723778
SOURCE (Princeton)LOC102723778
Genetics Home Reference (NIH)LOC102723778
Genomic and cartography
GoldenPath hg38 (UCSC)LOC102723778  -     chr4:31171144-31211674 +  4p15.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC102723778  -     4p15.1   [Description]    (hg19-Feb_2009)
EnsemblLOC102723778 - 4p15.1 [CytoView hg19]  LOC102723778 - 4p15.1 [CytoView hg38]
Mapping of homologs : NCBILOC102723778 [Mapview hg19]  LOC102723778 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI798927
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC102723778
Cluster EST : UnigeneHs.210739 [ NCBI ]
CGAP (NCI)Hs.210739
Alternative Splicing GalleryENSG00000251182
Gene ExpressionLOC102723778 [ NCBI-GEO ]   LOC102723778 [ EBI - ARRAY_EXPRESS ]   LOC102723778 [ SEEK ]   LOC102723778 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC102723778 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102723778
GTEX Portal (Tissue expression)LOC102723778
Human Protein AtlasENSG00000251182-LOC102723778 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC102723778
DMDM Disease mutations102723778
Blocks (Seattle)LOC102723778
Human Protein Atlas [tissue]ENSG00000251182-LOC102723778 [tissue]
Protein Interaction databases
FunCoupENSG00000251182
BioGRIDLOC102723778
STRING (EMBL)LOC102723778
ZODIACLOC102723778
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease102723778
BioCentury BCIQLOC102723778
ClinGenLOC102723778
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102723778
Clinical trialLOC102723778
Miscellaneous
canSAR (ICR)LOC102723778 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC102723778
EVEXLOC102723778
GoPubMedLOC102723778
iHOPLOC102723778
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 : Thu Nov 9 12:06:01 CET 2017

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