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CEP126 (centrosomal protein 126)

Identity

Alias_namesKIAA1377
KIAA1377
centrosomal protein 126kDa
Other alias
HGNC (Hugo) CEP126
LocusID (NCBI) 57562
Atlas_Id 77247
Location 11q22.1  [Link to chromosome band 11q22]
Location_base_pair Starts at 101915015 and ends at 102001065 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)
PANX1 (11q21) / CEP126 (11q22.1)

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)CEP126   29264
Cards
Entrez_Gene (NCBI)CEP126  57562  centrosomal protein 126
AliasesKIAA1377
GeneCards (Weizmann)CEP126
Ensembl hg19 (Hinxton)ENSG00000110318 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000110318 [Gene_View]  chr11:101915015-102001065 [Contig_View]  CEP126 [Vega]
ICGC DataPortalENSG00000110318
TCGA cBioPortalCEP126
AceView (NCBI)CEP126
Genatlas (Paris)CEP126
WikiGenes57562
SOURCE (Princeton)CEP126
Genetics Home Reference (NIH)CEP126
Genomic and cartography
GoldenPath hg38 (UCSC)CEP126  -     chr11:101915015-102001065 +  11q22.1   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)CEP126  -     11q22.1   [Description]    (hg19-Feb_2009)
EnsemblCEP126 - 11q22.1 [CytoView hg19]  CEP126 - 11q22.1 [CytoView hg38]
Mapping of homologs : NCBICEP126 [Mapview hg19]  CEP126 [Mapview hg38]
OMIM614634   
Gene and transcription
Genbank (Entrez)AB037798 AK057230 AK095004 AK296350 AK309479
RefSeq transcript (Entrez)NM_020802
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)CEP126
Cluster EST : UnigeneHs.156352 [ NCBI ]
CGAP (NCI)Hs.156352
Alternative Splicing GalleryENSG00000110318
Gene ExpressionCEP126 [ NCBI-GEO ]   CEP126 [ EBI - ARRAY_EXPRESS ]   CEP126 [ SEEK ]   CEP126 [ MEM ]
Gene Expression Viewer (FireBrowse)CEP126 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)57562
GTEX Portal (Tissue expression)CEP126
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9P2H0   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9P2H0  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9P2H0
Splice isoforms : SwissVarQ9P2H0
PhosPhoSitePlusQ9P2H0
Domains : Interpro (EBI)CEP126   
Domain families : Pfam (Sanger)K1377 (PF15352)   
Domain families : Pfam (NCBI)pfam15352   
Conserved Domain (NCBI)CEP126
DMDM Disease mutations57562
Blocks (Seattle)CEP126
SuperfamilyQ9P2H0
Human Protein AtlasENSG00000110318
Peptide AtlasQ9P2H0
HPRD17212
IPIIPI00159494   IPI01015847   IPI00984365   IPI00985189   
Protein Interaction databases
DIP (DOE-UCLA)Q9P2H0
IntAct (EBI)Q9P2H0
FunCoupENSG00000110318
BioGRIDCEP126
STRING (EMBL)CEP126
ZODIACCEP126
Ontologies - Pathways
QuickGOQ9P2H0
Ontology : AmiGOprotein binding  cytoplasm  centrosome  mitotic spindle organization  midbody  cytoplasmic microtubule organization  cilium assembly  ciliary base  non-motile cilium assembly  
Ontology : EGO-EBIprotein binding  cytoplasm  centrosome  mitotic spindle organization  midbody  cytoplasmic microtubule organization  cilium assembly  ciliary base  non-motile cilium assembly  
NDEx NetworkCEP126
Atlas of Cancer Signalling NetworkCEP126
Wikipedia pathwaysCEP126
Orthology - Evolution
OrthoDB57562
GeneTree (enSembl)ENSG00000110318
Phylogenetic Trees/Animal Genes : TreeFamCEP126
HOVERGENQ9P2H0
HOGENOMQ9P2H0
Homologs : HomoloGeneCEP126
Homology/Alignments : Family Browser (UCSC)CEP126
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerCEP126 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)CEP126
dbVarCEP126
ClinVarCEP126
1000_GenomesCEP126 
Exome Variant ServerCEP126
ExAC (Exome Aggregation Consortium)CEP126 (select the gene name)
Genetic variants : HAPMAP57562
Genomic Variants (DGV)CEP126 [DGVbeta]
DECIPHERCEP126 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisCEP126 
Mutations
ICGC Data PortalCEP126 
TCGA Data PortalCEP126 
Broad Tumor PortalCEP126
OASIS PortalCEP126 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDCEP126
BioMutasearch CEP126
DgiDB (Drug Gene Interaction Database)CEP126
DoCM (Curated mutations)CEP126 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)CEP126 (select a term)
intoGenCEP126
Cancer3DCEP126(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM614634   
Orphanet10874   
MedgenCEP126
Genetic Testing Registry CEP126
NextProtQ9P2H0 [Medical]
TSGene57562
GENETestsCEP126
Target ValidationCEP126
Huge Navigator CEP126 [HugePedia]
snp3D : Map Gene to Disease57562
BioCentury BCIQCEP126
ClinGenCEP126
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD57562
Chemical/Pharm GKB GenePA143485517
Clinical trialCEP126
Miscellaneous
canSAR (ICR)CEP126 (select the gene name)
Probes
Litterature
PubMed17 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineCEP126
EVEXCEP126
GoPubMedCEP126
iHOPCEP126
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 13:04:35 CEST 2017

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