Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC102723661 (uncharacterized LOC102723661)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 102723661
Atlas_Id 67692
Location 1p21.3  [Link to chromosome band 1p21]
Location_base_pair Starts at 95992068 and ends at 96022880 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)LOC102723661  102723661  uncharacterized LOC102723661
Aliases
GeneCards (Weizmann)LOC102723661
Ensembl hg19 (Hinxton)ENSG00000237435 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000237435 [Gene_View]  chr1:95992068-96022880 [Contig_View]  LOC102723661 [Vega]
ICGC DataPortalENSG00000237435
TCGA cBioPortalLOC102723661
AceView (NCBI)LOC102723661
Genatlas (Paris)LOC102723661
WikiGenes102723661
SOURCE (Princeton)LOC102723661
Genetics Home Reference (NIH)LOC102723661
Genomic and cartography
GoldenPath hg38 (UCSC)LOC102723661  -     chr1:95992068-96022880 +  1p21.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC102723661  -     1p21.3   [Description]    (hg19-Feb_2009)
EnsemblLOC102723661 - 1p21.3 [CytoView hg19]  LOC102723661 - 1p21.3 [CytoView hg38]
Mapping of homologs : NCBILOC102723661 [Mapview hg19]  LOC102723661 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI025778 BX095322
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC102723661
Cluster EST : UnigeneHs.143911 [ NCBI ]
CGAP (NCI)Hs.143911
Alternative Splicing GalleryENSG00000237435
Gene ExpressionLOC102723661 [ NCBI-GEO ]   LOC102723661 [ EBI - ARRAY_EXPRESS ]   LOC102723661 [ SEEK ]   LOC102723661 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC102723661 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)102723661
GTEX Portal (Tissue expression)LOC102723661
Human Protein AtlasENSG00000237435-LOC102723661 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC102723661
DMDM Disease mutations102723661
Blocks (Seattle)LOC102723661
Human Protein Atlas [tissue]ENSG00000237435-LOC102723661 [tissue]
Protein Interaction databases
FunCoupENSG00000237435
BioGRIDLOC102723661
STRING (EMBL)LOC102723661
ZODIACLOC102723661
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease102723661
BioCentury BCIQLOC102723661
ClinGenLOC102723661
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD102723661
Clinical trialLOC102723661
Miscellaneous
canSAR (ICR)LOC102723661 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC102723661
EVEXLOC102723661
GoPubMedLOC102723661
iHOPLOC102723661
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 12:05:58 CET 2017

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