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CCDC184 (coiled-coil domain containing 184)

Identity

Alias_namesC12orf68
chromosome 12 open reading frame 68
Alias_symbol (synonym)LOC387856
Other alias
HGNC (Hugo) CCDC184
LocusID (NCBI) 387856
Atlas_Id 61530
Location 12q13.11  [Link to chromosome band 12q13]
Location_base_pair Starts at 48183583 and ends at 48185926 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)CCDC184   33749
Cards
Entrez_Gene (NCBI)CCDC184  387856  coiled-coil domain containing 184
AliasesC12orf68
GeneCards (Weizmann)CCDC184
Ensembl hg19 (Hinxton)ENSG00000177875 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000177875 [Gene_View]  chr12:48183583-48185926 [Contig_View]  CCDC184 [Vega]
ICGC DataPortalENSG00000177875
TCGA cBioPortalCCDC184
AceView (NCBI)CCDC184
Genatlas (Paris)CCDC184
WikiGenes387856
SOURCE (Princeton)CCDC184
Genetics Home Reference (NIH)CCDC184
Genomic and cartography
GoldenPath hg38 (UCSC)CCDC184  -     chr12:48183583-48185926 +  12q13.11   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)CCDC184  -     12q13.11   [Description]    (hg19-Feb_2009)
EnsemblCCDC184 - 12q13.11 [CytoView hg19]  CCDC184 - 12q13.11 [CytoView hg38]
Mapping of homologs : NCBICCDC184 [Mapview hg19]  CCDC184 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK056003 AK056783 AM392860 BC036801 BC049387
RefSeq transcript (Entrez)NM_001013635
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)CCDC184
Cluster EST : UnigeneHs.251699 [ NCBI ]
CGAP (NCI)Hs.251699
Alternative Splicing GalleryENSG00000177875
Gene ExpressionCCDC184 [ NCBI-GEO ]   CCDC184 [ EBI - ARRAY_EXPRESS ]   CCDC184 [ SEEK ]   CCDC184 [ MEM ]
Gene Expression Viewer (FireBrowse)CCDC184 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)387856
GTEX Portal (Tissue expression)CCDC184
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ52MB2   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ52MB2  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ52MB2
Splice isoforms : SwissVarQ52MB2
PhosPhoSitePlusQ52MB2
Domains : Interpro (EBI)DUF4677   
Domain families : Pfam (Sanger)DUF4677 (PF15726)   
Domain families : Pfam (NCBI)pfam15726   
Conserved Domain (NCBI)CCDC184
DMDM Disease mutations387856
Blocks (Seattle)CCDC184
SuperfamilyQ52MB2
Human Protein AtlasENSG00000177875
Peptide AtlasQ52MB2
HPRD18375
IPIIPI00549500   IPI00984670   
Protein Interaction databases
DIP (DOE-UCLA)Q52MB2
IntAct (EBI)Q52MB2
FunCoupENSG00000177875
BioGRIDCCDC184
STRING (EMBL)CCDC184
ZODIACCCDC184
Ontologies - Pathways
QuickGOQ52MB2
Ontology : AmiGOprotein binding  cytoplasm  
Ontology : EGO-EBIprotein binding  cytoplasm  
NDEx NetworkCCDC184
Atlas of Cancer Signalling NetworkCCDC184
Wikipedia pathwaysCCDC184
Orthology - Evolution
OrthoDB387856
GeneTree (enSembl)ENSG00000177875
Phylogenetic Trees/Animal Genes : TreeFamCCDC184
HOVERGENQ52MB2
HOGENOMQ52MB2
Homologs : HomoloGeneCCDC184
Homology/Alignments : Family Browser (UCSC)CCDC184
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerCCDC184 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)CCDC184
dbVarCCDC184
ClinVarCCDC184
1000_GenomesCCDC184 
Exome Variant ServerCCDC184
ExAC (Exome Aggregation Consortium)CCDC184 (select the gene name)
Genetic variants : HAPMAP387856
Genomic Variants (DGV)CCDC184 [DGVbeta]
DECIPHERCCDC184 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisCCDC184 
Mutations
ICGC Data PortalCCDC184 
TCGA Data PortalCCDC184 
Broad Tumor PortalCCDC184
OASIS PortalCCDC184 [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDCCDC184
BioMutasearch CCDC184
DgiDB (Drug Gene Interaction Database)CCDC184
DoCM (Curated mutations)CCDC184 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)CCDC184 (select a term)
intoGenCCDC184
Cancer3DCCDC184(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenCCDC184
Genetic Testing Registry CCDC184
NextProtQ52MB2 [Medical]
TSGene387856
GENETestsCCDC184
Target ValidationCCDC184
Huge Navigator CCDC184 [HugePedia]
snp3D : Map Gene to Disease387856
BioCentury BCIQCCDC184
ClinGenCCDC184
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD387856
Chemical/Pharm GKB GenePA162377998
Clinical trialCCDC184
Miscellaneous
canSAR (ICR)CCDC184 (select the gene name)
Probes
Litterature
PubMed9 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineCCDC184
EVEXCCDC184
GoPubMedCCDC184
iHOPCCDC184
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 13:04:09 CEST 2017

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