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CENPI (centromere protein I)

Identity

Alias (NCBI)CENP-I
FSHPRH1
LRPR1
HGNC (Hugo) CENPI
HGNC Alias symbLRPR1
CENP-I
Mis6
HGNC Previous nameFSHPRH1
HGNC Previous nameFSH primary response (LRPR1, rat) homolog 1
 FSH primary response (LRPR1 homolog, rat) 1
LocusID (NCBI) 2491
Atlas_Id 57689
Location Xq22.1  [Link to chromosome band Xq22]
Location_base_pair Starts at 101099809 and ends at 101163673 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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    centromere protein I
AliasesCENP-I; FSHPRH1; LRPR1
GeneCards (Weizmann)CENPI
Ensembl hg19 (Hinxton)ENSG00000102384 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000102384 [Gene_View]  ENSG00000102384 [Sequence]  chrX:101099809-101163673 [Contig_View]  CENPI [Vega]
ICGC DataPortalENSG00000102384
TCGA cBioPortalCENPI
AceView (NCBI)CENPI
Genatlas (Paris)CENPI
SOURCE (Princeton)CENPI
Genetics Home Reference (NIH)CENPI
Genomic and cartography
GoldenPath hg38 (UCSC)CENPI  -     chrX:101099809-101163673 +  Xq22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)CENPI  -     Xq22.1   [Description]    (hg19-Feb_2009)
GoldenPathCENPI - Xq22.1 [CytoView hg19]  CENPI - Xq22.1 [CytoView hg38]
ImmunoBaseENSG00000102384
Genome Data Viewer NCBICENPI [Mapview hg19]  
OMIM300065   
Gene and transcription
Genbank (Entrez)AK302986 BC005967 BC012462 BF204027 BG114761
RefSeq transcript (Entrez)NM_001318521 NM_001318523 NM_001386188 NM_006733
Consensus coding sequences : CCDS (NCBI)CENPI
Gene ExpressionCENPI [ NCBI-GEO ]   CENPI [ EBI - ARRAY_EXPRESS ]   CENPI [ SEEK ]   CENPI [ MEM ]
Gene Expression Viewer (FireBrowse)CENPI [ Firebrowse - Broad ]
GenevisibleExpression of CENPI in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)2491
GTEX Portal (Tissue expression)CENPI
Human Protein AtlasENSG00000102384-CENPI [pathology]   [cell]   [tissue]
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
PhosPhoSitePlusQ92674
Domains : Interpro (EBI)CENP-I   
Domain families : Pfam (Sanger)CENP-I (PF07778)   
Domain families : Pfam (NCBI)pfam07778   
Conserved Domain (NCBI)CENPI
SuperfamilyQ92674
AlphaFold pdb e-kbQ92674   
Human Protein Atlas [tissue]ENSG00000102384-CENPI [tissue]
Protein Interaction databases
DIP (DOE-UCLA)Q92674
IntAct (EBI)Q92674
BioGRIDCENPI
STRING (EMBL)CENPI
ZODIACCENPI
Ontologies - Pathways
QuickGOQ92674
Ontology : AmiGOkinetochore  kinetochore  protein binding  nucleoplasm  cytosol  cytosol  cytosol  mitotic spindle organization  sex differentiation  nuclear body  nuclear body  CENP-A containing nucleosome assembly  
Ontology : EGO-EBIkinetochore  kinetochore  protein binding  nucleoplasm  cytosol  cytosol  cytosol  mitotic spindle organization  sex differentiation  nuclear body  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
Homologs : HomoloGeneCENPI
Homology/Alignments : Family Browser (UCSC)CENPI
Gene fusions - Rearrangements
Fusion : QuiverCENPI
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerCENPI [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)CENPI
dbVarCENPI
ClinVarCENPI
MonarchCENPI
1000_GenomesCENPI 
Exome Variant ServerCENPI
GNOMAD BrowserENSG00000102384
Varsome BrowserCENPI
ACMGCENPI variants
VarityQ92674
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]  
Somatic Mutations in Cancer : COSMIC3DCENPI
Mutations and Diseases : HGMDCENPI
LOVD (Leiden Open Variation Database)[gene] [transcripts] [variants]
BioMutaCENPI
DgiDB (Drug Gene Interaction Database)CENPI
DoCM (Curated mutations)CENPI
CIViC (Clinical Interpretations of Variants in Cancer)CENPI
Cancer3DCENPI
Impact of mutations[PolyPhen2] [Provean] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM300065   
Orphanet
DisGeNETCENPI
MedgenCENPI
Genetic Testing Registry CENPI
NextProtQ92674 [Medical]
GENETestsCENPI
Target ValidationCENPI
Huge Navigator CENPI [HugePedia]
ClinGenCENPI
Clinical trials, drugs, therapy
MyCancerGenomeCENPI
Protein Interactions : CTDCENPI
Pharm GKB GenePA28385
PharosQ92674
Clinical trialCENPI
Miscellaneous
canSAR (ICR)CENPI
HarmonizomeCENPI
DataMed IndexCENPI
Probes
Litterature
PubMed30 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
EVEXCENPI
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Mon Oct 4 15:03:31 CEST 2021

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