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DNAH10OS (dynein axonemal heavy chain 10 opposite strand)

Identity

Alias_namesdynein, axonemal, heavy chain 10 opposite strand (non-protein coding)
Alias_symbol (synonym)FLJ45278
Other alias-
HGNC (Hugo) DNAH10OS
LocusID (NCBI) 642797
Atlas_Id 62545
Location 12_KI270834v1_alt  [Link to chromosome band 12]
Location_base_pair Starts at 100599 and ends at 108528 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


External links

Nomenclature
HGNC (Hugo)DNAH10OS   37121
Cards
Entrez_Gene (NCBI)DNAH10OS  642797  dynein axonemal heavy chain 10 opposite strand
Aliases
GeneCards (Weizmann)DNAH10OS
Ensembl hg19 (Hinxton)ENSG00000250091 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000250091 [Gene_View]  chr12_KI270834v1_alt:100599-108528 [Contig_View]  DNAH10OS [Vega]
ICGC DataPortalENSG00000250091
TCGA cBioPortalDNAH10OS
AceView (NCBI)DNAH10OS
Genatlas (Paris)DNAH10OS
WikiGenes642797
SOURCE (Princeton)DNAH10OS
Genetics Home Reference (NIH)DNAH10OS
Genomic and cartography
GoldenPath hg38 (UCSC)DNAH10OS  -     chr12_KI270834v1_alt:100599-108528 -  12_KI270834v1_alt   [Description]    (hg38-Dec_2013)
GoldenPath hg19 (UCSC)DNAH10OS  -     12_KI270834v1_alt   [Description]    (hg19-Feb_2009)
EnsemblDNAH10OS - 12_KI270834v1_alt [CytoView hg19]  DNAH10OS - 12_KI270834v1_alt [CytoView hg38]
Mapping of homologs : NCBIDNAH10OS [Mapview hg19]  DNAH10OS [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK127211
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)DNAH10OS
Cluster EST : UnigeneHs.728379 [ NCBI ]
CGAP (NCI)Hs.728379
Alternative Splicing GalleryENSG00000250091
Gene ExpressionDNAH10OS [ NCBI-GEO ]   DNAH10OS [ EBI - ARRAY_EXPRESS ]   DNAH10OS [ SEEK ]   DNAH10OS [ MEM ]
Gene Expression Viewer (FireBrowse)DNAH10OS [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevestigatorExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)642797
GTEX Portal (Tissue expression)DNAH10OS
Human Protein AtlasENSG00000250091-DNAH10OS [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
UniProt/SwissProtP0CZ25   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtP0CZ25  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProP0CZ25
Splice isoforms : SwissVarP0CZ25
PhosPhoSitePlusP0CZ25
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)DNAH10OS
DMDM Disease mutations642797
Blocks (Seattle)DNAH10OS
SuperfamilyP0CZ25
Human Protein Atlas [tissue]ENSG00000250091-DNAH10OS [tissue]
Peptide AtlasP0CZ25
IPIIPI00964182   
Protein Interaction databases
DIP (DOE-UCLA)P0CZ25
IntAct (EBI)P0CZ25
FunCoupENSG00000250091
BioGRIDDNAH10OS
STRING (EMBL)DNAH10OS
ZODIACDNAH10OS
Ontologies - Pathways
QuickGOP0CZ25
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkDNAH10OS
Atlas of Cancer Signalling NetworkDNAH10OS
Wikipedia pathwaysDNAH10OS
Orthology - Evolution
OrthoDB642797
GeneTree (enSembl)ENSG00000250091
Phylogenetic Trees/Animal Genes : TreeFamDNAH10OS
HOVERGENP0CZ25
HOGENOMP0CZ25
Homologs : HomoloGeneDNAH10OS
Homology/Alignments : Family Browser (UCSC)DNAH10OS
Gene fusions - Rearrangements
Tumor Fusion PortalDNAH10OS
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerDNAH10OS [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)DNAH10OS
dbVarDNAH10OS
ClinVarDNAH10OS
1000_GenomesDNAH10OS 
Exome Variant ServerDNAH10OS
ExAC (Exome Aggregation Consortium)ENSG00000250091
GNOMAD BrowserENSG00000250091
Genetic variants : HAPMAP642797
Genomic Variants (DGV)DNAH10OS [DGVbeta]
DECIPHERDNAH10OS [patients]   [syndromes]   [variants]   [genes]  
CONAN: Copy Number AnalysisDNAH10OS 
Mutations
ICGC Data PortalDNAH10OS 
TCGA Data PortalDNAH10OS 
Broad Tumor PortalDNAH10OS
OASIS PortalDNAH10OS [ Somatic mutations - Copy number]
Mutations and Diseases : HGMDDNAH10OS
BioMutasearch DNAH10OS
DgiDB (Drug Gene Interaction Database)DNAH10OS
DoCM (Curated mutations)DNAH10OS (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)DNAH10OS (select a term)
intoGenDNAH10OS
Cancer3DDNAH10OS(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
DisGeNETDNAH10OS
MedgenDNAH10OS
Genetic Testing Registry DNAH10OS
NextProtP0CZ25 [Medical]
TSGene642797
GENETestsDNAH10OS
Target ValidationDNAH10OS
Huge Navigator DNAH10OS [HugePedia]
snp3D : Map Gene to Disease642797
BioCentury BCIQDNAH10OS
ClinGenDNAH10OS
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD642797
Chemical/Pharm GKB GenePA165512563
Clinical trialDNAH10OS
Miscellaneous
canSAR (ICR)DNAH10OS (select the gene name)
Probes
Litterature
PubMed2 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineDNAH10OS
EVEXDNAH10OS
GoPubMedDNAH10OS
iHOPDNAH10OS
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 Nov 21 13:26:04 CET 2017

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