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C10orf32 (chromosome 10 open reading frame 32)

Identity

Other alias-
HGNC (Hugo) C10orf32
LocusID (NCBI) 119032
Atlas_Id 60861
Location 10q24.32  [Link to chromosome band 10q24]
Location_base_pair Starts at 104613967 and ends at 104624718 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)C10orf32   23516
Cards
Entrez_Gene (NCBI)C10orf32  119032  chromosome 10 open reading frame 32
Aliases
GeneCards (Weizmann)C10orf32
Ensembl hg19 (Hinxton)ENSG00000166275 [Gene_View]  chr10:104613967-104624718 [Contig_View]  C10orf32 [Vega]
Ensembl hg38 (Hinxton)ENSG00000166275 [Gene_View]  chr10:104613967-104624718 [Contig_View]  C10orf32 [Vega]
ICGC DataPortalENSG00000166275
TCGA cBioPortalC10orf32
AceView (NCBI)C10orf32
Genatlas (Paris)C10orf32
WikiGenes119032
SOURCE (Princeton)C10orf32
Genetics Home Reference (NIH)C10orf32
Genomic and cartography
GoldenPath hg19 (UCSC)C10orf32  -     chr10:104613967-104624718 +  10q24.32   [Description]    (hg19-Feb_2009)
GoldenPath hg38 (UCSC)C10orf32  -     10q24.32   [Description]    (hg38-Dec_2013)
EnsemblC10orf32 - 10q24.32 [CytoView hg19]  C10orf32 - 10q24.32 [CytoView hg38]
Mapping of homologs : NCBIC10orf32 [Mapview hg19]  C10orf32 [Mapview hg38]
Gene and transcription
Genbank (Entrez)AA299084 AI147530 AK098071 AK311742 AL832477
RefSeq transcript (Entrez)NM_001136200 NM_144591
RefSeq genomic (Entrez)NC_000010 NC_018921 NT_030059 NW_004929376
Consensus coding sequences : CCDS (NCBI)C10orf32
Cluster EST : UnigeneHs.34492 [ NCBI ]
CGAP (NCI)Hs.34492
Alternative Splicing GalleryENSG00000166275
Gene ExpressionC10orf32 [ NCBI-GEO ]   C10orf32 [ EBI - ARRAY_EXPRESS ]   C10orf32 [ SEEK ]   C10orf32 [ MEM ]
Gene Expression Viewer (FireBrowse)C10orf32 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
GenevisibleExpression in : [tissues]  [cell-lines]  [cancer]  [perturbations]  
BioGPS (Tissue expression)119032
GTEX Portal (Tissue expression)C10orf32
Protein : pattern, domain, 3D structure
UniProt/SwissProtQ96B45   [function]  [subcellular_location]  [family_and_domains]  [pathology_and_biotech]  [ptm_processing]  [expression]  [interaction]
NextProtQ96B45  [Sequence]  [Exons]  [Medical]  [Publications]
With graphics : InterProQ96B45
Splice isoforms : SwissVarQ96B45
PhosPhoSitePlusQ96B45
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C10orf32
DMDM Disease mutations119032
Blocks (Seattle)C10orf32
SuperfamilyQ96B45
Human Protein AtlasENSG00000166275
Peptide AtlasQ96B45
HPRD12571
IPIIPI00303253   
Protein Interaction databases
DIP (DOE-UCLA)Q96B45
IntAct (EBI)Q96B45
FunCoupENSG00000166275
BioGRIDC10orf32
STRING (EMBL)C10orf32
ZODIACC10orf32
Ontologies - Pathways
QuickGOQ96B45
Ontology : AmiGO
Ontology : EGO-EBI
NDEx NetworkC10orf32
Atlas of Cancer Signalling NetworkC10orf32
Wikipedia pathwaysC10orf32
Orthology - Evolution
OrthoDB119032
GeneTree (enSembl)ENSG00000166275
Phylogenetic Trees/Animal Genes : TreeFamC10orf32
HOVERGENQ96B45
HOGENOMQ96B45
Homologs : HomoloGeneC10orf32
Homology/Alignments : Family Browser (UCSC)C10orf32
Gene fusions - Rearrangements
Polymorphisms : SNP and Copy number variants
NCBI Variation ViewerC10orf32 [hg38]
dbSNP Single Nucleotide Polymorphism (NCBI)C10orf32
dbVarC10orf32
ClinVarC10orf32
1000_GenomesC10orf32 
Exome Variant ServerC10orf32
ExAC (Exome Aggregation Consortium)C10orf32 (select the gene name)
Genetic variants : HAPMAP119032
Genomic Variants (DGV)C10orf32 [DGVbeta]
DECIPHER (Syndromes)10:104613967-104624718  ENSG00000166275
CONAN: Copy Number AnalysisC10orf32 
Mutations
ICGC Data PortalC10orf32 
TCGA Data PortalC10orf32 
Broad Tumor PortalC10orf32
OASIS PortalC10orf32 [ Somatic mutations - Copy number]
Somatic Mutations in Cancer : COSMICC10orf32  [overview]  [genome browser]  [tissue]  [distribution]  
Mutations and Diseases : HGMDC10orf32
LOVD (Leiden Open Variation Database)Whole genome datasets
LOVD (Leiden Open Variation Database)LOVD 3.0 shared installation
BioMutasearch C10orf32
DgiDB (Drug Gene Interaction Database)C10orf32
DoCM (Curated mutations)C10orf32 (select the gene name)
CIViC (Clinical Interpretations of Variants in Cancer)C10orf32 (select a term)
intoGenC10orf32
Cancer3DC10orf32(select the gene name)
Impact of mutations[PolyPhen2] [SIFT Human Coding SNP] [Buck Institute : MutDB] [Mutation Assessor] [Mutanalyser]
Diseases
OMIM
Orphanet
MedgenC10orf32
Genetic Testing Registry C10orf32
NextProtQ96B45 [Medical]
TSGene119032
GENETestsC10orf32
Huge Navigator C10orf32 [HugePedia]
snp3D : Map Gene to Disease119032
BioCentury BCIQC10orf32
ClinGenC10orf32
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD119032
Chemical/Pharm GKB GenePA134928831
Clinical trialC10orf32
Miscellaneous
canSAR (ICR)C10orf32 (select the gene name)
Probes
Litterature
PubMed11 Pubmed reference(s) in Entrez
GeneRIFsGene References Into Functions (Entrez)
CoreMineC10orf32
EVEXC10orf32
GoPubMedC10orf32
iHOPC10orf32
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 11:56:13 CET 2017

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