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C14orf132 (chromosome 14 open reading frame 132)

Identity

Alias_namesC14orf88
chromosome 14 open reading frame 88
Other alias
HGNC (Hugo) C14orf132
LocusID (NCBI) 56967
Atlas_Id 60929
Location 14q32.2  [Link to chromosome band 14q32]
Location_base_pair Starts at 96505661 and ends at 96560308 bp from pter ( according to hg19-Feb_2009)
Fusion genes
(updated 2016)
DARS (2q21.3) / C14orf132 (14q32.2)MACROD2 (20p12.1) / C14orf132 (14q32.2)RPS6 (9p22.1) / C14orf132 (14q32.2)
RPS6KA5 (14q32.11) / C14orf132 (14q32.2)SMAP1 (6q13) / C14orf132 (14q32.2)RPS6KA5 C14orf132
SMAP1 C14orf132

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)C14orf132   20346
Cards
Entrez_Gene (NCBI)C14orf132  56967  chromosome 14 open reading frame 132
AliasesC14orf88
GeneCards (Weizmann)C14orf132
Ensembl hg19 (Hinxton) [Gene_View]  chr14:96505661-96560308 [Contig_View]  C14orf132 [Vega]
Ensembl hg38 (Hinxton) [Gene_View]  chr14:96505661-96560308 [Contig_View]  C14orf132 [Vega]
TCGA cBioPortalC14orf132
AceView (NCBI)C14orf132
Genatlas (Paris)C14orf132
WikiGenes56967
SOURCE (Princeton)C14orf132
Genetics Home Reference (NIH)C14orf132
Genomic and cartography
GoldenPath hg19 (UCSC)C14orf132  -     chr14:96505661-96560308 +  14q32.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)C14orf132  -     14q32.2   [Description]    (hg38-Dec_2013)
EnsemblC14orf132 - 14q32.2 [CytoView hg19]  C14orf132 - 14q32.2 [CytoView hg38]
Mapping of homologs : NCBIC14orf132 [Mapview hg19]  C14orf132 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AB621830 AF131832 AK001590 AK022021 AK025915
RefSeq transcript (Entrez)NM_001252507 NM_001282463 NM_001282464 NM_001289139 NM_020215
RefSeq genomic (Entrez)NC_000014 NC_018925 NT_026437 NW_004929393
Consensus coding sequences : CCDS (NCBI)C14orf132
Cluster EST : UnigeneHs.733033 [ NCBI ]
CGAP (NCI)Hs.733033
Gene ExpressionC14orf132 [ NCBI-GEO ]   C14orf132 [ EBI - ARRAY_EXPRESS ]   C14orf132 [ SEEK ]   C14orf132 [ MEM ]
Gene Expression Viewer (FireBrowse)C14orf132 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)56967
GTEX Portal (Tissue expression)C14orf132
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9NPU4   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9NPU4  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9NPU4
Splice isoforms : SwissVarQ9NPU4
PhosPhoSitePlusQ9NPU4
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C14orf132
DMDM Disease mutations56967
Blocks (Seattle)C14orf132
SuperfamilyQ9NPU4
Peptide AtlasQ9NPU4
HPRD16603
IPIIPI00024938   
Protein Interaction databases
DIP (DOE-UCLA)Q9NPU4
IntAct (EBI)Q9NPU4
BioGRIDC14orf132
STRING (EMBL)C14orf132
ZODIACC14orf132
Ontologies - Pathways
QuickGOQ9NPU4
Ontology : AmiGOintegral component of membrane  
Ontology : EGO-EBIintegral component of membrane  
NDEx NetworkC14orf132
Atlas of Cancer Signalling NetworkC14orf132
Wikipedia pathwaysC14orf132
Orthology - Evolution
OrthoDB56967
Phylogenetic Trees/Animal Genes : TreeFamC14orf132
HOVERGENQ9NPU4
HOGENOMQ9NPU4
Homologs : HomoloGeneC14orf132
Homology/Alignments : Family Browser (UCSC)C14orf132
Gene fusions - Rearrangements
Fusion: TCGARPS6KA5 C14orf132
Fusion: TCGASMAP1 C14orf132
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC14orf132 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C14orf132
dbVarC14orf132
ClinVarC14orf132
1000_GenomesC14orf132 
Exome Variant ServerC14orf132
ExAC (Exome Aggregation Consortium)C14orf132 (select the gene name)
Genetic variants : HAPMAP56967
Genomic Variants (DGV)C14orf132 [DGVbeta]
DECIPHER (Syndromes)14:96505661-96560308  
CONAN: Copy Number AnalysisC14orf132 
Mutations
ICGC Data PortalC14orf132 
TCGA Data PortalC14orf132 
Broad Tumor PortalC14orf132
OASIS PortalC14orf132 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC14orf132  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDC14orf132
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch C14orf132
DgiDB (Drug Gene Interaction Database)C14orf132
DoCM (Curated mutations)C14orf132 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C14orf132 (select a term)
intoGenC14orf132
Cancer3DC14orf132(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenC14orf132
Genetic Testing Registry C14orf132
NextProtQ9NPU4 [Medical]
TSGene56967
GENETestsC14orf132
Huge Navigator C14orf132 [HugePedia]
snp3D : Map Gene to Disease56967
BioCentury BCIQC14orf132
ClinGenC14orf132
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD56967
Chemical/Pharm GKB GenePA134860941
Clinical trialC14orf132
Miscellaneous
canSAR (ICR)C14orf132 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC14orf132
EVEXC14orf132
GoPubMedC14orf132
iHOPC14orf132
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Mar 14 11:56:28 CET 2017

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