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C14orf105 (chromosome 14 open reading frame 105)

Identity

Alias_symbol (synonym)FLJ10650
Other alias-
HGNC (Hugo) C14orf105
LocusID (NCBI) 55195
Atlas_Id 60927
Location 14q22.3  [Link to chromosome band 14q22]
Location_base_pair Starts at 57469300 and ends at 57493863 bp from pter ( according to hg38-Dec_2013)
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)

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)C14orf105   20189
Cards
Entrez_Gene (NCBI)C14orf105  55195  chromosome 14 open reading frame 105
Aliases
GeneCards (Weizmann)C14orf105
Ensembl hg19 (Hinxton)ENSG00000100557 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000100557 [Gene_View]  chr14:57469300-57493863 [Contig_View]  C14orf105 [Vega]
ICGC DataPortalENSG00000100557
TCGA cBioPortalC14orf105
AceView (NCBI)C14orf105
Genatlas (Paris)C14orf105
WikiGenes55195
SOURCE (Princeton)C14orf105
Genetics Home Reference (NIH)C14orf105
Genomic and cartography
GoldenPath hg38 (UCSC)C14orf105  -     chr14:57469300-57493863 -  14q22.3   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)C14orf105  -     14q22.3   [Description]    (hg19-Feb_2009)
EnsemblC14orf105 - 14q22.3 [CytoView hg19]  C14orf105 - 14q22.3 [CytoView hg38]
Mapping of homologs : NCBIC14orf105 [Mapview hg19]  C14orf105 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AI733133 AK001512 AK223127 AK307238 BC028060
RefSeq transcript (Entrez)NM_001283056 NM_001283057 NM_001283058 NM_001283059 NM_001283060 NM_018168
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)C14orf105
Cluster EST : UnigeneHs.659706 [ NCBI ]
CGAP (NCI)Hs.659706
Alternative Splicing GalleryENSG00000100557
Gene ExpressionC14orf105 [ NCBI-GEO ]   C14orf105 [ EBI - ARRAY_EXPRESS ]   C14orf105 [ SEEK ]   C14orf105 [ MEM ]
Gene Expression Viewer (FireBrowse)C14orf105 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)55195
GTEX Portal (Tissue expression)C14orf105
Human Protein AtlasENSG00000100557-C14orf105 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9NVL8   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9NVL8  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9NVL8
Splice isoforms : SwissVarQ9NVL8
PhosPhoSitePlusQ9NVL8
Domains : Interpro (EBI)DUF4619   
Domain families : Pfam (Sanger)DUF4619 (PF15398)   
Domain families : Pfam (NCBI)pfam15398   
Conserved Domain (NCBI)C14orf105
DMDM Disease mutations55195
Blocks (Seattle)C14orf105
SuperfamilyQ9NVL8
Human Protein Atlas [tissue]ENSG00000100557-C14orf105 [tissue]
Peptide AtlasQ9NVL8
HPRD12628
IPIIPI00018805   IPI00981609   IPI00984251   IPI00807622   IPI00982014   IPI00921799   
Protein Interaction databases
DIP (DOE-UCLA)Q9NVL8
IntAct (EBI)Q9NVL8
FunCoupENSG00000100557
BioGRIDC14orf105
STRING (EMBL)C14orf105
ZODIACC14orf105
Ontologies - Pathways
QuickGOQ9NVL8
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkC14orf105
Atlas of Cancer Signalling NetworkC14orf105
Wikipedia pathwaysC14orf105
Orthology - Evolution
OrthoDB55195
GeneTree (enSembl)ENSG00000100557
Phylogenetic Trees/Animal Genes : TreeFamC14orf105
HOVERGENQ9NVL8
HOGENOMQ9NVL8
Homologs : HomoloGeneC14orf105
Homology/Alignments : Family Browser (UCSC)C14orf105
Gene fusions - Rearrangements
Tumor Fusion PortalC14orf105
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC14orf105 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C14orf105
dbVarC14orf105
ClinVarC14orf105
1000_GenomesC14orf105 
Exome Variant ServerC14orf105
ExAC (Exome Aggregation Consortium)ENSG00000100557
GNOMAD BrowserENSG00000100557
Genetic variants : HAPMAP55195
Genomic Variants (DGV)C14orf105 [DGVbeta]
DECIPHERC14orf105 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisC14orf105 
Mutations
ICGC Data PortalC14orf105 
TCGA Data PortalC14orf105 
Broad Tumor PortalC14orf105
OASIS PortalC14orf105 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC14orf105  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDC14orf105
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 C14orf105
DgiDB (Drug Gene Interaction Database)C14orf105
DoCM (Curated mutations)C14orf105 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C14orf105 (select a term)
intoGenC14orf105
Cancer3DC14orf105(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETC14orf105
MedgenC14orf105
Genetic Testing Registry C14orf105
NextProtQ9NVL8 [Medical]
TSGene55195
GENETestsC14orf105
Target ValidationC14orf105
Huge Navigator C14orf105 [HugePedia]
snp3D : Map Gene to Disease55195
BioCentury BCIQC14orf105
ClinGenC14orf105
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD55195
Chemical/Pharm GKB GenePA134868494
Clinical trialC14orf105
Miscellaneous
canSAR (ICR)C14orf105 (select the gene name)
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC14orf105
EVEXC14orf105
GoPubMedC14orf105
iHOPC14orf105
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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indexed on : Tue Nov 21 13:44:40 CET 2017

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