Atlas of Genetics and Cytogenetics in Oncology and Haematology


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LOC100286922 (DnaJ (Hsp40) homolog, subfamily B, member 3 pseudogene)

Identity

Other alias-
HGNC (Hugo) -
LocusID (NCBI) 100286922
Atlas_Id 66619
Location 2q37.1  [Link to chromosome band 2q37]
Location_base_pair Starts at 234662962 and ends at 234663991 bp from pter ( according to hg19-Feb_2009)

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)LOC100286922  100286922  DnaJ (Hsp40) homolog, subfamily B, member 3 pseudogene
Aliases
GeneCards (Weizmann)LOC100286922
Ensembl hg19 (Hinxton) [Gene_View]  chr2:234662962-234663991 [Contig_View]  LOC100286922 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr2:234662962-234663991 [Contig_View]  LOC100286922 [Vega]
TCGA cBioPortalLOC100286922
AceView (NCBI)LOC100286922
Genatlas (Paris)LOC100286922
WikiGenes100286922
SOURCE (Princeton)LOC100286922
Genetics Home Reference (NIH)LOC100286922
Genomic and cartography
GoldenPath hg19 (UCSC)LOC100286922  -     chr2:234662962-234663991 -  2q37.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)LOC100286922  -     2q37.1   [Description]    (hg38-Dec_2013)
EnsemblLOC100286922 - 2q37.1 [CytoView hg19]  LOC100286922 - 2q37.1 [CytoView hg38]
Mapping of homologs : NCBILOC100286922 [Mapview hg19]  LOC100286922 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA912512 AI126471 AI807912 BC066346 BX102479
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)NC_000002 NC_018913 NG_002601 NT_005403 NW_004929306
Consensus coding sequences : CCDS (NCBI)LOC100286922
Cluster EST : UnigeneHs.124112 [ NCBI ]
CGAP (NCI)Hs.124112
Gene ExpressionLOC100286922 [ NCBI-GEO ]   LOC100286922 [ EBI - ARRAY_EXPRESS ]   LOC100286922 [ SEEK ]   LOC100286922 [ MEM ]
Gene Expression Viewer (FireBrowse)LOC100286922 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)100286922
GTEX Portal (Tissue expression)LOC100286922
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)LOC100286922
DMDM Disease mutations100286922
Blocks (Seattle)LOC100286922
Protein Interaction databases
BioGRIDLOC100286922
STRING (EMBL)LOC100286922
ZODIACLOC100286922
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease100286922
BioCentury BCIQLOC100286922
ClinGenLOC100286922
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100286922
Clinical trialLOC100286922
Miscellaneous
canSAR (ICR)LOC100286922 (select the gene name)
Probes
Litterature
PubMed1 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineLOC100286922
EVEXLOC100286922
GoPubMedLOC100286922
iHOPLOC100286922
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 : Tue Mar 14 12:16:20 CET 2017

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