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C14orf119 (chromosome 14 open reading frame 119)

Identity

Alias_symbol (synonym)FLJ20671
Other alias-
HGNC (Hugo) C14orf119
LocusID (NCBI) 55017
Atlas_Id 60928
Location 14q11.2  [Link to chromosome band 14q11]
Location_base_pair Starts at 23564683 and ends at 23569665 bp from pter ( according to hg19-Feb_2009)

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)C14orf119   20270
Cards
Entrez_Gene (NCBI)C14orf119  55017  chromosome 14 open reading frame 119
Aliases
GeneCards (Weizmann)C14orf119
Ensembl hg19 (Hinxton)ENSG00000179933 [Gene_View]  chr14:23564683-23569665 [Contig_View]  C14orf119 [Vega]
Ensembl hg38 (Hinxton)ENSG00000179933 [Gene_View]  chr14:23564683-23569665 [Contig_View]  C14orf119 [Vega]
ICGC DataPortalENSG00000179933
TCGA cBioPortalC14orf119
AceView (NCBI)C14orf119
Genatlas (Paris)C14orf119
WikiGenes55017
SOURCE (Princeton)C14orf119
Genetics Home Reference (NIH)C14orf119
Genomic and cartography
GoldenPath hg19 (UCSC)C14orf119  -     chr14:23564683-23569665 +  14q11.2   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)C14orf119  -     14q11.2   [Description]    (hg38-Dec_2013)
EnsemblC14orf119 - 14q11.2 [CytoView hg19]  C14orf119 - 14q11.2 [CytoView hg38]
Mapping of homologs : NCBIC14orf119 [Mapview hg19]  C14orf119 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AF061731 AK000678 AK024794 BC009645 BC056255
RefSeq transcript (Entrez)NM_017924
RefSeq genomic (Entrez)NC_000014 NC_018925 NG_030461 NT_026437 NW_004929393
Consensus coding sequences : CCDS (NCBI)C14orf119
Cluster EST : UnigeneHs.735365 [ NCBI ]
CGAP (NCI)Hs.735365
Alternative Splicing GalleryENSG00000179933
Gene ExpressionC14orf119 [ NCBI-GEO ]   C14orf119 [ EBI - ARRAY_EXPRESS ]   C14orf119 [ SEEK ]   C14orf119 [ MEM ]
Gene Expression Viewer (FireBrowse)C14orf119 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)55017
GTEX Portal (Tissue expression)C14orf119
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9NWQ9   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9NWQ9  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9NWQ9
Splice isoforms : SwissVarQ9NWQ9
PhosPhoSitePlusQ9NWQ9
Domains : Interpro (EBI)DUF4508   
Domain families : Pfam (Sanger)DUF4508 (PF14969)   
Domain families : Pfam (NCBI)pfam14969   
Conserved Domain (NCBI)C14orf119
DMDM Disease mutations55017
Blocks (Seattle)C14orf119
SuperfamilyQ9NWQ9
Human Protein AtlasENSG00000179933
Peptide AtlasQ9NWQ9
HPRD16595
IPIIPI00016726   
Protein Interaction databases
DIP (DOE-UCLA)Q9NWQ9
IntAct (EBI)Q9NWQ9
FunCoupENSG00000179933
BioGRIDC14orf119
STRING (EMBL)C14orf119
ZODIACC14orf119
Ontologies - Pathways
QuickGOQ9NWQ9
Ontology : AmiGOmitochondrion  
Ontology : EGO-EBImitochondrion  
NDEx NetworkC14orf119
Atlas of Cancer Signalling NetworkC14orf119
Wikipedia pathwaysC14orf119
Orthology - Evolution
OrthoDB55017
GeneTree (enSembl)ENSG00000179933
Phylogenetic Trees/Animal Genes : TreeFamC14orf119
HOVERGENQ9NWQ9
HOGENOMQ9NWQ9
Homologs : HomoloGeneC14orf119
Homology/Alignments : Family Browser (UCSC)C14orf119
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC14orf119 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C14orf119
dbVarC14orf119
ClinVarC14orf119
1000_GenomesC14orf119 
Exome Variant ServerC14orf119
ExAC (Exome Aggregation Consortium)C14orf119 (select the gene name)
Genetic variants : HAPMAP55017
Genomic Variants (DGV)C14orf119 [DGVbeta]
DECIPHER (Syndromes)14:23564683-23569665  ENSG00000179933
CONAN: Copy Number AnalysisC14orf119 
Mutations
ICGC Data PortalC14orf119 
TCGA Data PortalC14orf119 
Broad Tumor PortalC14orf119
OASIS PortalC14orf119 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC14orf119  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDC14orf119
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch C14orf119
DgiDB (Drug Gene Interaction Database)C14orf119
DoCM (Curated mutations)C14orf119 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C14orf119 (select a term)
intoGenC14orf119
Cancer3DC14orf119(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenC14orf119
Genetic Testing Registry C14orf119
NextProtQ9NWQ9 [Medical]
TSGene55017
GENETestsC14orf119
Huge Navigator C14orf119 [HugePedia]
snp3D : Map Gene to Disease55017
BioCentury BCIQC14orf119
ClinGenC14orf119
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD55017
Chemical/Pharm GKB GenePA134974692
Clinical trialC14orf119
Miscellaneous
canSAR (ICR)C14orf119 (select the gene name)
Probes
Litterature
PubMed7 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC14orf119
EVEXC14orf119
GoPubMedC14orf119
iHOPC14orf119
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Mar 14 11:56:28 CET 2017

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