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C15orf26 (chromosome 15 open reading frame 26)

Identity

Other alias-
HGNC (Hugo) C15orf26
LocusID (NCBI) 161502
Atlas_Id 60945
Location 15q25.1  [Link to chromosome band 15q25]
Location_base_pair Starts at 81426644 and ends at 81441516 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)C15orf26   26782
Cards
Entrez_Gene (NCBI)C15orf26  161502  chromosome 15 open reading frame 26
Aliases
GeneCards (Weizmann)C15orf26
Ensembl hg19 (Hinxton)ENSG00000156206 [Gene_View]  chr15:81426644-81441516 [Contig_View]  C15orf26 [Vega]
Ensembl hg38 (Hinxton)ENSG00000156206 [Gene_View]  chr15:81426644-81441516 [Contig_View]  C15orf26 [Vega]
ICGC DataPortalENSG00000156206
TCGA cBioPortalC15orf26
AceView (NCBI)C15orf26
Genatlas (Paris)C15orf26
WikiGenes161502
SOURCE (Princeton)C15orf26
Genetics Home Reference (NIH)C15orf26
Genomic and cartography
GoldenPath hg19 (UCSC)C15orf26  -     chr15:81426644-81441516 +  15q25.1   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)C15orf26  -     15q25.1   [Description]    (hg38-Dec_2013)
EnsemblC15orf26 - 15q25.1 [CytoView hg19]  C15orf26 - 15q25.1 [CytoView hg38]
Mapping of homologs : NCBIC15orf26 [Mapview hg19]  C15orf26 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK095934 AK302120 AK307565 BC062471
RefSeq transcript (Entrez)NM_173528
RefSeq genomic (Entrez)NC_000015 NC_018926 NT_010194 NW_004929398
Consensus coding sequences : CCDS (NCBI)C15orf26
Cluster EST : UnigeneHs.130979 [ NCBI ]
CGAP (NCI)Hs.130979
Alternative Splicing GalleryENSG00000156206
Gene ExpressionC15orf26 [ NCBI-GEO ]   C15orf26 [ EBI - ARRAY_EXPRESS ]   C15orf26 [ SEEK ]   C15orf26 [ MEM ]
Gene Expression Viewer (FireBrowse)C15orf26 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)161502
GTEX Portal (Tissue expression)C15orf26
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ6P656   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ6P656  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ6P656
Splice isoforms : SwissVarQ6P656
PhosPhoSitePlusQ6P656
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C15orf26
DMDM Disease mutations161502
Blocks (Seattle)C15orf26
SuperfamilyQ6P656
Human Protein AtlasENSG00000156206
Peptide AtlasQ6P656
HPRD08243
IPIIPI00760712   IPI00441064   
Protein Interaction databases
DIP (DOE-UCLA)Q6P656
IntAct (EBI)Q6P656
FunCoupENSG00000156206
BioGRIDC15orf26
STRING (EMBL)C15orf26
ZODIACC15orf26
Ontologies - Pathways
QuickGOQ6P656
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkC15orf26
Atlas of Cancer Signalling NetworkC15orf26
Wikipedia pathwaysC15orf26
Orthology - Evolution
OrthoDB161502
GeneTree (enSembl)ENSG00000156206
Phylogenetic Trees/Animal Genes : TreeFamC15orf26
HOVERGENQ6P656
HOGENOMQ6P656
Homologs : HomoloGeneC15orf26
Homology/Alignments : Family Browser (UCSC)C15orf26
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC15orf26 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C15orf26
dbVarC15orf26
ClinVarC15orf26
1000_GenomesC15orf26 
Exome Variant ServerC15orf26
ExAC (Exome Aggregation Consortium)C15orf26 (select the gene name)
Genetic variants : HAPMAP161502
Genomic Variants (DGV)C15orf26 [DGVbeta]
DECIPHER (Syndromes)15:81426644-81441516  ENSG00000156206
CONAN: Copy Number AnalysisC15orf26 
Mutations
ICGC Data PortalC15orf26 
TCGA Data PortalC15orf26 
Broad Tumor PortalC15orf26
OASIS PortalC15orf26 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC15orf26  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDC15orf26
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 C15orf26
DgiDB (Drug Gene Interaction Database)C15orf26
DoCM (Curated mutations)C15orf26 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C15orf26 (select a term)
intoGenC15orf26
Cancer3DC15orf26(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenC15orf26
Genetic Testing Registry C15orf26
NextProtQ6P656 [Medical]
TSGene161502
GENETestsC15orf26
Huge Navigator C15orf26 [HugePedia]
snp3D : Map Gene to Disease161502
BioCentury BCIQC15orf26
ClinGenC15orf26
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD161502
Chemical/Pharm GKB GenePA134908662
Clinical trialC15orf26
Miscellaneous
canSAR (ICR)C15orf26 (select the gene name)
Probes
Litterature
PubMed3 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC15orf26
EVEXC15orf26
GoPubMedC15orf26
iHOPC15orf26
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 11:56:31 CET 2017

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