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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 12q24.31  [Link to chromosome band 12q24]
Location_base_pair Starts at 124411602 and ends at 124419531 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


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]  chr12:124411602-124419531 [Contig_View]  DNAH10OS [Vega]
Ensembl hg38 (Hinxton)ENSG00000250091 [Gene_View]  chr12:124411602-124419531 [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 hg19 (UCSC)DNAH10OS  -     chr12:124411602-124419531 -  12q24.31   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)DNAH10OS  -     12q24.31   [Description]    (hg38-Dec_2013)
EnsemblDNAH10OS - 12q24.31 [CytoView hg19]  DNAH10OS - 12q24.31 [CytoView hg38]
Mapping of homologs : NCBIDNAH10OS [Mapview hg19]  DNAH10OS [Mapview hg38]
Gene and transcription
Genbank (Entrez)AK127211
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)AC_000144 NC_000012 NT_009755 NW_001838064
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]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)642797
GTEX Portal (Tissue expression)DNAH10OS
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 AtlasENSG00000250091
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
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)DNAH10OS (select the gene name)
Genetic variants : HAPMAP642797
Genomic Variants (DGV)DNAH10OS [DGVbeta]
DECIPHER (Syndromes)12:124411602-124419531  ENSG00000250091
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
MedgenDNAH10OS
Genetic Testing Registry DNAH10OS
NextProtP0CZ25 [Medical]
TSGene642797
GENETestsDNAH10OS
Huge Navigator DNAH10OS [HugePedia]
snp3D : Map Gene to Disease642797
BioCentury BCIQDNAH10OS
ClinGenDNAH10OS
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD642797
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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indexed on : Tue Mar 14 12:01:54 CET 2017

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