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CDC123 (cell division cycle 123)

Identity

Alias_namesC10orf7
chromosome 10 open reading frame 7
cell division cycle 123 homolog (S. cerevisiae)
Alias_symbol (synonym)D123
Other alias
HGNC (Hugo) CDC123
LocusID (NCBI) 8872
Atlas_Id 56084
Location 10p14  [Link to chromosome band 10p14]
Location_base_pair Starts at 12195962 and ends at 12250590 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2016)		PRPF18 (10p13) / CDC123 (10p13)

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)CDC123   16827
Cards
Entrez_Gene (NCBI)CDC123  8872  cell division cycle 123
AliasesC10orf7; D123
GeneCards (Weizmann)CDC123
Ensembl hg19 (Hinxton)ENSG00000151465 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000151465 [Gene_View]  chr10:12195962-12250590 [Contig_View]  CDC123 [Vega]
ICGC DataPortalENSG00000151465
TCGA cBioPortalCDC123
AceView (NCBI)CDC123
Genatlas (Paris)CDC123
WikiGenes8872
SOURCE (Princeton)CDC123
Genetics Home Reference (NIH)CDC123
Genomic and cartography
GoldenPath hg38 (UCSC)CDC123  -     chr10:12195962-12250590 +  10p14   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)CDC123  -     10p14   [Description]    (hg19-Feb_2009)
EnsemblCDC123 - 10p14 [CytoView hg19]  CDC123 - 10p14 [CytoView hg38]
Mapping of homologs : NCBICDC123 [Mapview hg19]  CDC123 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK023925 AK225634 AK289362 AK308790 AW006077
RefSeq transcript (Entrez)NM_006023
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)CDC123
Cluster EST : UnigeneHs.703246 [ NCBI ]
CGAP (NCI)Hs.703246
Alternative Splicing GalleryENSG00000151465
Gene ExpressionCDC123 [ NCBI-GEO ]   CDC123 [ EBI - ARRAY_EXPRESS ]   CDC123 [ SEEK ]   CDC123 [ MEM ]
Gene Expression Viewer (FireBrowse)CDC123 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)8872
GTEX Portal (Tissue expression)CDC123
Protein : pattern, domain, 3D structure
UniProt/SwissProtO75794   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtO75794  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProO75794
Splice isoforms : SwissVarO75794
PhosPhoSitePlusO75794
Domains : Interpro (EBI)CDC123   
Domain families : Pfam (Sanger)D123 (PF07065)   
Domain families : Pfam (NCBI)pfam07065   
Conserved Domain (NCBI)CDC123
DMDM Disease mutations8872
Blocks (Seattle)CDC123
SuperfamilyO75794
Human Protein AtlasENSG00000151465
Peptide AtlasO75794
HPRD12586
IPIIPI00005670   IPI00883779   IPI00515030   IPI00514360   IPI00641917   IPI00514175   IPI00647355   
Protein Interaction databases
DIP (DOE-UCLA)O75794
IntAct (EBI)O75794
FunCoupENSG00000151465
BioGRIDCDC123
STRING (EMBL)CDC123
ZODIACCDC123
Ontologies - Pathways
QuickGOO75794
Ontology : AmiGOcytoplasm  regulation of translation  cell cycle arrest  positive regulation of cell proliferation  positive regulation of translational initiation  cell division  eukaryotic translation initiation factor 2 complex assembly  
Ontology : EGO-EBIcytoplasm  regulation of translation  cell cycle arrest  positive regulation of cell proliferation  positive regulation of translational initiation  cell division  eukaryotic translation initiation factor 2 complex assembly  
NDEx NetworkCDC123
Atlas of Cancer Signalling NetworkCDC123
Wikipedia pathwaysCDC123
Orthology - Evolution
OrthoDB8872
GeneTree (enSembl)ENSG00000151465
Phylogenetic Trees/Animal Genes : TreeFamCDC123
HOVERGENO75794
HOGENOMO75794
Homologs : HomoloGeneCDC123
Homology/Alignments : Family Browser (UCSC)CDC123
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerCDC123 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)CDC123
dbVarCDC123
ClinVarCDC123
1000_GenomesCDC123 
Exome Variant ServerCDC123
ExAC (Exome Aggregation Consortium)CDC123 (select the gene name)
Genetic variants : HAPMAP8872
Genomic Variants (DGV)CDC123 [DGVbeta]
DECIPHERCDC123 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisCDC123 
Mutations
ICGC Data PortalCDC123 
TCGA Data PortalCDC123 
Broad Tumor PortalCDC123
OASIS PortalCDC123 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICCDC123  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDCDC123
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 CDC123
DgiDB (Drug Gene Interaction Database)CDC123
DoCM (Curated mutations)CDC123 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)CDC123 (select a term)
intoGenCDC123
Cancer3DCDC123(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenCDC123
Genetic Testing Registry CDC123
NextProtO75794 [Medical]
TSGene8872
GENETestsCDC123
Target ValidationCDC123
Huge Navigator CDC123 [HugePedia]
snp3D : Map Gene to Disease8872
BioCentury BCIQCDC123
ClinGenCDC123
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD8872
Chemical/Pharm GKB GenePA162382148
Clinical trialCDC123
Miscellaneous
canSAR (ICR)CDC123 (select the gene name)
Probes
Litterature
PubMed52 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineCDC123
EVEXCDC123
GoPubMedCDC123
iHOPCDC123
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 25 19:01:27 CEST 2017
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