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CENPI (centromere protein I)

Identity

Alias_namesFSHPRH1
FSH primary response (LRPR1, rat) homolog 1
FSH primary response (LRPR1 homolog, rat) 1
Alias_symbol (synonym)LRPR1
CENP-I
Mis6
Other alias
HGNC (Hugo) CENPI
LocusID (NCBI) 2491
Atlas_Id 61705
Location Xq22.1  [Link to chromosome band Xq22]
Location_base_pair Starts at 101098182 and ends at 101163673 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)CENPI   3968
Cards
Entrez_Gene (NCBI)CENPI  2491  centromere protein I
AliasesCENP-I; FSHPRH1; LRPR1
GeneCards (Weizmann)CENPI
Ensembl hg19 (Hinxton)ENSG00000102384 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000102384 [Gene_View]  chrX:101098182-101163673 [Contig_View]  CENPI [Vega]
ICGC DataPortalENSG00000102384
TCGA cBioPortalCENPI
AceView (NCBI)CENPI
Genatlas (Paris)CENPI
WikiGenes2491
SOURCE (Princeton)CENPI
Genetics Home Reference (NIH)CENPI
Genomic and cartography
GoldenPath hg38 (UCSC)CENPI  -     chrX:101098182-101163673 +  Xq22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)CENPI  -     Xq22.1   [Description]    (hg19-Feb_2009)
EnsemblCENPI - Xq22.1 [CytoView hg19]  CENPI - Xq22.1 [CytoView hg38]
Mapping of homologs : NCBICENPI [Mapview hg19]  CENPI [Mapview hg38]
OMIM300065   
Gene and transcription
Genbank (Entrez)AK302986 BC005967 BC012462 BF204027 BG114761
RefSeq transcript (Entrez)NM_001318521 NM_001318523 NM_006733
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)CENPI
Cluster EST : UnigeneHs.737663 [ NCBI ]
CGAP (NCI)Hs.737663
Alternative Splicing GalleryENSG00000102384
Gene ExpressionCENPI [ NCBI-GEO ]   CENPI [ EBI - ARRAY_EXPRESS ]   CENPI [ SEEK ]   CENPI [ MEM ]
Gene Expression Viewer (FireBrowse)CENPI [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)2491
GTEX Portal (Tissue expression)CENPI
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ92674   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ92674  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ92674
Splice isoforms : SwissVarQ92674
PhosPhoSitePlusQ92674
Domains : Interpro (EBI)CENP-I   
Domain families : Pfam (Sanger)CENP-I (PF07778)   
Domain families : Pfam (NCBI)pfam07778   
Conserved Domain (NCBI)CENPI
DMDM Disease mutations2491
Blocks (Seattle)CENPI
SuperfamilyQ92674
Human Protein AtlasENSG00000102384
Peptide AtlasQ92674
HPRD02089
IPIIPI00552142   IPI00647405   IPI00645634   IPI00644001   
Protein Interaction databases
DIP (DOE-UCLA)Q92674
IntAct (EBI)Q92674
FunCoupENSG00000102384
BioGRIDCENPI
STRING (EMBL)CENPI
ZODIACCENPI
Ontologies - Pathways
QuickGOQ92674
Ontology : AmiGOkinetochore  protein binding  nucleoplasm  cytosol  cytosol  sister chromatid cohesion  sex differentiation  nuclear body  CENP-A containing nucleosome assembly  
Ontology : EGO-EBIkinetochore  protein binding  nucleoplasm  cytosol  cytosol  sister chromatid cohesion  sex differentiation  nuclear body  CENP-A containing nucleosome assembly  
NDEx NetworkCENPI
Atlas of Cancer Signalling NetworkCENPI
Wikipedia pathwaysCENPI
Orthology - Evolution
OrthoDB2491
GeneTree (enSembl)ENSG00000102384
Phylogenetic Trees/Animal Genes : TreeFamCENPI
HOVERGENQ92674
HOGENOMQ92674
Homologs : HomoloGeneCENPI
Homology/Alignments : Family Browser (UCSC)CENPI
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerCENPI [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)CENPI
dbVarCENPI
ClinVarCENPI
1000_GenomesCENPI 
Exome Variant ServerCENPI
ExAC (Exome Aggregation Consortium)CENPI (select the gene name)
Genetic variants : HAPMAP2491
Genomic Variants (DGV)CENPI [DGVbeta]
DECIPHERCENPI [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisCENPI 
Mutations
ICGC Data PortalCENPI 
TCGA Data PortalCENPI 
Broad Tumor PortalCENPI
OASIS PortalCENPI [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICCENPI  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDCENPI
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
LOVD (Leiden Open Variation Database)X-chromosome gene database
BioMutasearch CENPI
DgiDB (Drug Gene Interaction Database)CENPI
DoCM (Curated mutations)CENPI (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)CENPI (select a term)
intoGenCENPI
Cancer3DCENPI(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300065   
Orphanet
MedgenCENPI
Genetic Testing Registry CENPI
NextProtQ92674 [Medical]
TSGene2491
GENETestsCENPI
Target ValidationCENPI
Huge Navigator CENPI [HugePedia]
snp3D : Map Gene to Disease2491
BioCentury BCIQCENPI
ClinGenCENPI
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD2491
Chemical/Pharm GKB GenePA28385
Clinical trialCENPI
Miscellaneous
canSAR (ICR)CENPI (select the gene name)
Probes
Litterature
PubMed21 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineCENPI
EVEXCENPI
GoPubMedCENPI
iHOPCENPI
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Wed Jun 7 15:43:11 CEST 2017

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