Atlas of Genetics and Cytogenetics in Oncology and Haematology


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C10orf95 (chromosome 10 open reading frame 95)

Identity

Alias_symbol (synonym)FLJ14280
Other alias-
HGNC (Hugo) C10orf95
LocusID (NCBI) 79946
Atlas_Id 60874
Location 10q24.32  [Link to chromosome band 10q24]
Location_base_pair Starts at 102449837 and ends at 102451543 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)C10orf95   25880
Cards
Entrez_Gene (NCBI)C10orf95  79946  chromosome 10 open reading frame 95
Aliases
GeneCards (Weizmann)C10orf95
Ensembl hg19 (Hinxton) [Gene_View]
Ensembl hg38 (Hinxton) [Gene_View]  chr10:102449837-102451543 [Contig_View]  C10orf95 [Vega]
TCGA cBioPortalC10orf95
AceView (NCBI)C10orf95
Genatlas (Paris)C10orf95
WikiGenes79946
SOURCE (Princeton)C10orf95
Genetics Home Reference (NIH)C10orf95
Genomic and cartography
GoldenPath hg38 (UCSC)C10orf95  -     chr10:102449837-102451543 -  10q24.32   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)C10orf95  -     10q24.32   [Description]    (hg19-Feb_2009)
EnsemblC10orf95 - 10q24.32 [CytoView hg19]  C10orf95 - 10q24.32 [CytoView hg38]
Mapping of homologs : NCBIC10orf95 [Mapview hg19]  C10orf95 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK024342 BC126459
RefSeq transcript (Entrez)NM_024886
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)C10orf95
Cluster EST : UnigeneHs.225084 [ NCBI ]
CGAP (NCI)Hs.225084
Gene ExpressionC10orf95 [ NCBI-GEO ]   C10orf95 [ EBI - ARRAY_EXPRESS ]   C10orf95 [ SEEK ]   C10orf95 [ MEM ]
Gene Expression Viewer (FireBrowse)C10orf95 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)79946
GTEX Portal (Tissue expression)C10orf95
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ9H7T3   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ9H7T3  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ9H7T3
Splice isoforms : SwissVarQ9H7T3
PhosPhoSitePlusQ9H7T3
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C10orf95
DMDM Disease mutations79946
Blocks (Seattle)C10orf95
SuperfamilyQ9H7T3
Peptide AtlasQ9H7T3
HPRD10701
IPIIPI00016462   
Protein Interaction databases
DIP (DOE-UCLA)Q9H7T3
IntAct (EBI)Q9H7T3
BioGRIDC10orf95
STRING (EMBL)C10orf95
ZODIACC10orf95
Ontologies - Pathways
QuickGOQ9H7T3
Ontology : AmiGOprotein binding  
Ontology : EGO-EBIprotein binding  
NDEx NetworkC10orf95
Atlas of Cancer Signalling NetworkC10orf95
Wikipedia pathwaysC10orf95
Orthology - Evolution
OrthoDB79946
Phylogenetic Trees/Animal Genes : TreeFamC10orf95
HOVERGENQ9H7T3
HOGENOMQ9H7T3
Homologs : HomoloGeneC10orf95
Homology/Alignments : Family Browser (UCSC)C10orf95
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC10orf95 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C10orf95
dbVarC10orf95
ClinVarC10orf95
1000_GenomesC10orf95 
Exome Variant ServerC10orf95
ExAC (Exome Aggregation Consortium)C10orf95 (select the gene name)
Genetic variants : HAPMAP79946
Genomic Variants (DGV)C10orf95 [DGVbeta]
DECIPHERC10orf95 [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisC10orf95 
Mutations
ICGC Data PortalC10orf95 
TCGA Data PortalC10orf95 
Broad Tumor PortalC10orf95
OASIS PortalC10orf95 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC10orf95  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDC10orf95
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch C10orf95
DgiDB (Drug Gene Interaction Database)C10orf95
DoCM (Curated mutations)C10orf95 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C10orf95 (select a term)
intoGenC10orf95
Cancer3DC10orf95(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenC10orf95
Genetic Testing Registry C10orf95
NextProtQ9H7T3 [Medical]
TSGene79946
GENETestsC10orf95
Target ValidationC10orf95
Huge Navigator C10orf95 [HugePedia]
snp3D : Map Gene to Disease79946
BioCentury BCIQC10orf95
ClinGenC10orf95
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD79946
Chemical/Pharm GKB GenePA134908188
Clinical trialC10orf95
Miscellaneous
canSAR (ICR)C10orf95 (select the gene name)
Probes
Litterature
PubMed6 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC10orf95
EVEXC10orf95
GoPubMedC10orf95
iHOPC10orf95
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 : Wed Jun 7 15:40:08 CEST 2017

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