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PRR32 (proline rich 32)

Identity

Alias_namesCXorf64
chromosome X open reading frame 64
Other alias
HGNC (Hugo) PRR32
LocusID (NCBI) 100130613
Atlas_Id 72282
Location Xq25  [Link to chromosome band Xq25]
Location_base_pair Starts at 126819764 and ends at 126821785 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)PRR32   34498
Cards
Entrez_Gene (NCBI)PRR32  100130613  proline rich 32
AliasesCXorf64
GeneCards (Weizmann)PRR32
Ensembl hg19 (Hinxton)ENSG00000183631 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000183631 [Gene_View]  chrX:126819764-126821785 [Contig_View]  PRR32 [Vega]
ICGC DataPortalENSG00000183631
TCGA cBioPortalPRR32
AceView (NCBI)PRR32
Genatlas (Paris)PRR32
WikiGenes100130613
SOURCE (Princeton)PRR32
Genetics Home Reference (NIH)PRR32
Genomic and cartography
GoldenPath hg38 (UCSC)PRR32  -     chrX:126819764-126821785 +  Xq25   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)PRR32  -     Xq25   [Description]    (hg19-Feb_2009)
EnsemblPRR32 - Xq25 [CytoView hg19]  PRR32 - Xq25 [CytoView hg38]
Mapping of homologs : NCBIPRR32 [Mapview hg19]  PRR32 [Mapview hg38]
Gene and transcription
Genbank (Entrez)BG200532 CA433109 R10182
RefSeq transcript (Entrez)NM_001122716
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)PRR32
Cluster EST : UnigeneHs.130370 [ NCBI ]
CGAP (NCI)Hs.130370
Alternative Splicing GalleryENSG00000183631
Gene ExpressionPRR32 [ NCBI-GEO ]   PRR32 [ EBI - ARRAY_EXPRESS ]   PRR32 [ SEEK ]   PRR32 [ MEM ]
Gene Expression Viewer (FireBrowse)PRR32 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)100130613
GTEX Portal (Tissue expression)PRR32
Protein : pattern, domain, 3D structure
UniProt/SwissProtB1ATL7   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtB1ATL7  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProB1ATL7
Splice isoforms : SwissVarB1ATL7
PhosPhoSitePlusB1ATL7
Domains : Interpro (EBI)DUF4645   
Domain families : Pfam (Sanger)DUF4645 (PF15488)   
Domain families : Pfam (NCBI)pfam15488   
Conserved Domain (NCBI)PRR32
DMDM Disease mutations100130613
Blocks (Seattle)PRR32
SuperfamilyB1ATL7
Human Protein AtlasENSG00000183631
Peptide AtlasB1ATL7
IPIIPI00232876   
Protein Interaction databases
DIP (DOE-UCLA)B1ATL7
IntAct (EBI)B1ATL7
FunCoupENSG00000183631
BioGRIDPRR32
STRING (EMBL)PRR32
ZODIACPRR32
Ontologies - Pathways
QuickGOB1ATL7
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkPRR32
Atlas of Cancer Signalling NetworkPRR32
Wikipedia pathwaysPRR32
Orthology - Evolution
OrthoDB100130613
GeneTree (enSembl)ENSG00000183631
Phylogenetic Trees/Animal Genes : TreeFamPRR32
HOVERGENB1ATL7
HOGENOMB1ATL7
Homologs : HomoloGenePRR32
Homology/Alignments : Family Browser (UCSC)PRR32
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerPRR32 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)PRR32
dbVarPRR32
ClinVarPRR32
1000_GenomesPRR32 
Exome Variant ServerPRR32
ExAC (Exome Aggregation Consortium)PRR32 (select the gene name)
Genetic variants : HAPMAP100130613
Genomic Variants (DGV)PRR32 [DGVbeta]
DECIPHERPRR32 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisPRR32 
Mutations
ICGC Data PortalPRR32 
TCGA Data PortalPRR32 
Broad Tumor PortalPRR32
OASIS PortalPRR32 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDPRR32
BioMutasearch PRR32
DgiDB (Drug Gene Interaction Database)PRR32
DoCM (Curated mutations)PRR32 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)PRR32 (select a term)
intoGenPRR32
Cancer3DPRR32(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenPRR32
Genetic Testing Registry PRR32
NextProtB1ATL7 [Medical]
TSGene100130613
GENETestsPRR32
Target ValidationPRR32
Huge Navigator PRR32 [HugePedia]
snp3D : Map Gene to Disease100130613
BioCentury BCIQPRR32
ClinGenPRR32
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD100130613
Chemical/Pharm GKB GenePA162383082
Clinical trialPRR32
Miscellaneous
canSAR (ICR)PRR32 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMinePRR32
EVEXPRR32
GoPubMedPRR32
iHOPPRR32
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Sep 18 13:35:25 CEST 2017

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