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LOC100131347 (RAD52 motif containing 1 pseudogene)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100131347
Atlas_Id 66480
Location 17q12  [Link to chromosome band 17q12]
Location_base_pair Starts at 39057019 and ends at 39081451 bp from pter ( according to hg38-Dec_2013)

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)LOC100131347  100131347  RAD52 motif containing 1 pseudogene
Aliases
GeneCards (Weizmann)LOC100131347
Ensembl hg19 (Hinxton)ENSG00000263818 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000263818 [Gene_View]  chr17:39057019-39081451 [Contig_View]  LOC100131347 [Vega]
ICGC DataPortalENSG00000263818
TCGA cBioPortalLOC100131347
AceView (NCBI)LOC100131347
Genatlas (Paris)LOC100131347
WikiGenes100131347
SOURCE (Princeton)LOC100131347
Genetics Home Reference (NIH)LOC100131347
Genomic and cartography
GoldenPath hg38 (UCSC)LOC100131347  -     chr17:39057019-39081451 +  17q12   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)LOC100131347  -     17q12   [Description]    (hg19-Feb_2009)
EnsemblLOC100131347 - 17q12 [CytoView hg19]  LOC100131347 - 17q12 [CytoView hg38]
Mapping of homologs : NCBILOC100131347 [Mapview hg19]  LOC100131347 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK095115 AK124220 BC072408
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)LOC100131347
Cluster EST : UnigeneHs.676510 [ NCBI ]
CGAP (NCI)Hs.676510
Alternative Splicing GalleryENSG00000263818
Gene ExpressionLOC100131347 [ NCBI-GEO ]   LOC100131347 [ EBI - ARRAY_EXPRESS ]   LOC100131347 [ SEEK ]   LOC100131347 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100131347 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100131347
GTEX Portal (Tissue expression)LOC100131347
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100131347
DMDM Disease mutations100131347
Blocks (Seattle)LOC100131347
Human Protein AtlasENSG00000263818
IPIIPI00743832   IPI00978720   
Protein Interaction databases
FunCoupENSG00000263818
BioGRIDLOC100131347
STRING (EMBL)LOC100131347
ZODIACLOC100131347
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100131347
BioCentury BCIQLOC100131347
ClinGenLOC100131347
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100131347
Clinical trialLOC100131347
Miscellaneous
canSAR (ICR)LOC100131347 (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100131347
EVEXLOC100131347
GoPubMedLOC100131347
iHOPLOC100131347
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 : Mon Sep 18 13:17:47 CEST 2017

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