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QRICH2 (glutamine rich 2)

Identity

Alias_symbol (synonym)DKFZP434P0316
Other alias-
HGNC (Hugo) QRICH2
LocusID (NCBI) 84074
Atlas_Id 72443
Location 17q25.1  [Link to chromosome band 17q25]
Location_base_pair Starts at 74270130 and ends at 74303761 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
CASKIN2 (17q25.1) / QRICH2 (17q25.1)QRICH2 (17q25.1) / QRICH2 (17q25.1)

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)QRICH2   25326
Cards
Entrez_Gene (NCBI)QRICH2  84074  glutamine rich 2
Aliases
GeneCards (Weizmann)QRICH2
Ensembl hg19 (Hinxton)ENSG00000129646 [Gene_View]  chr17:74270130-74303761 [Contig_View]  QRICH2 [Vega]
Ensembl hg38 (Hinxton)ENSG00000129646 [Gene_View]  chr17:74270130-74303761 [Contig_View]  QRICH2 [Vega]
ICGC DataPortalENSG00000129646
TCGA cBioPortalQRICH2
AceView (NCBI)QRICH2
Genatlas (Paris)QRICH2
WikiGenes84074
SOURCE (Princeton)QRICH2
Genetics Home Reference (NIH)QRICH2
Genomic and cartography
GoldenPath hg19 (UCSC)QRICH2  -     chr17:74270130-74303761 -  17q25.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)QRICH2  -     17q25.1   [Description]    (hg38-Dec_2013)
EnsemblQRICH2 - 17q25.1 [CytoView hg19]  QRICH2 - 17q25.1 [CytoView hg38]
Mapping of homologs : NCBIQRICH2 [Mapview hg19]  QRICH2 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK058102 AL136774 BC131559 EU832276 EU832361
RefSeq transcript (Entrez)NM_032134
RefSeq genomic (Entrez)NC_000017 NC_018928 NT_010783 NW_004929407
Consensus coding sequences : CCDS (NCBI)QRICH2
Cluster EST : UnigeneHs.252739 [ NCBI ]
CGAP (NCI)Hs.252739
Alternative Splicing GalleryENSG00000129646
Gene ExpressionQRICH2 [ NCBI-GEO ]   QRICH2 [ EBI - ARRAY_EXPRESS ]   QRICH2 [ SEEK ]   QRICH2 [ MEM ]
Gene Expression Viewer (FireBrowse)QRICH2 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)84074
GTEX Portal (Tissue expression)QRICH2
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9H0J4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9H0J4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9H0J4
Splice isoforms : SwissVarQ9H0J4
PhosPhoSitePlusQ9H0J4
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)QRICH2
DMDM Disease mutations84074
Blocks (Seattle)QRICH2
SuperfamilyQ9H0J4
Human Protein AtlasENSG00000129646
Peptide AtlasQ9H0J4
HPRD10891
IPIIPI00030267   IPI00105119   IPI00854858   IPI00914046   IPI00952578   IPI00978304   IPI00981619   
Protein Interaction databases
DIP (DOE-UCLA)Q9H0J4
IntAct (EBI)Q9H0J4
FunCoupENSG00000129646
BioGRIDQRICH2
STRING (EMBL)QRICH2
ZODIACQRICH2
Ontologies - Pathways
QuickGOQ9H0J4
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkQRICH2
Atlas of Cancer Signalling NetworkQRICH2
Wikipedia pathwaysQRICH2
Orthology - Evolution
OrthoDB84074
GeneTree (enSembl)ENSG00000129646
Phylogenetic Trees/Animal Genes : TreeFamQRICH2
HOVERGENQ9H0J4
HOGENOMQ9H0J4
Homologs : HomoloGeneQRICH2
Homology/Alignments : Family Browser (UCSC)QRICH2
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerQRICH2 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)QRICH2
dbVarQRICH2
ClinVarQRICH2
1000_GenomesQRICH2 
Exome Variant ServerQRICH2
ExAC (Exome Aggregation Consortium)QRICH2 (select the gene name)
Genetic variants : HAPMAP84074
Genomic Variants (DGV)QRICH2 [DGVbeta]
DECIPHER (Syndromes)17:74270130-74303761  ENSG00000129646
CONAN: Copy Number AnalysisQRICH2 
Mutations
ICGC Data PortalQRICH2 
TCGA Data PortalQRICH2 
Broad Tumor PortalQRICH2
OASIS PortalQRICH2 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICQRICH2  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDQRICH2
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD - Leiden Open Variation Database
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch QRICH2
DgiDB (Drug Gene Interaction Database)QRICH2
DoCM (Curated mutations)QRICH2 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)QRICH2 (select a term)
intoGenQRICH2
Cancer3DQRICH2(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenQRICH2
Genetic Testing Registry QRICH2
NextProtQ9H0J4 [Medical]
TSGene84074
GENETestsQRICH2
Huge Navigator QRICH2 [HugePedia]
snp3D : Map Gene to Disease84074
BioCentury BCIQQRICH2
ClinGenQRICH2
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD84074
Chemical/Pharm GKB GenePA142671107
Clinical trialQRICH2
Miscellaneous
canSAR (ICR)QRICH2 (select the gene name)
Probes
Litterature
PubMed4 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineQRICH2
EVEXQRICH2
GoPubMedQRICH2
iHOPQRICH2
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

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indexed on : Tue Mar 14 12:40:24 CET 2017

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