Atlas of Genetics and Cytogenetics in Oncology and Haematology


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C21orf33 (-)

Identity

Alias_symbol (synonym)KNP-Ia
GT335
ES1
HES1
D21S2048E
KNPI
KNPH
KNP-I
Other alias-
HGNC (Hugo) -
LocusID (NCBI) 8209
Atlas_Id 883
Location -  [Link to chromosome band ]
Fusion genes
(updated 2017)
Data from Atlas, Mitelman, Cosmic Fusion, Fusion Cancer, TCGA fusion databases with official HUGO symbols (see references in chromosomal bands)
C21orf33 (21q22.3) / CAPNS1 (19q13.12)C21orf33 (21q22.3) / TAZ (Xq28)

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)-   -
Cards
Entrez_Gene (NCBI)C21orf33  8209  -
Aliases
GeneCards (Weizmann)C21orf33
Ensembl hg19 (Hinxton)ENSG00000160221 [Gene_View]
Ensembl hg38 (Hinxton)ENSG00000160221 [Gene_View]  ENSG00000160221 [Sequence]  - [Contig_View]  C21orf33 [Vega]
ICGC DataPortalENSG00000160221
TCGA cBioPortalC21orf33
AceView (NCBI)C21orf33
Genatlas (Paris)C21orf33
WikiGenes8209
SOURCE (Princeton)C21orf33
Genetics Home Reference (NIH)C21orf33
Genomic and cartography
GoldenPath hg38 (UCSC)C21orf33  -  
GoldenPath hg19 (UCSC)C21orf33  -  
EnsemblC21orf33 - [CytoView hg19]  C21orf33 - [CytoView hg38]
Mapping of homologs : NCBIC21orf33 [Mapview hg19]  C21orf33 [Mapview hg38]
Gene and transcription
Genbank (Entrez)-
RefSeq transcript (Entrez)
RefSeq genomic (Entrez)
Consensus coding sequences : CCDS (NCBI)C21orf33
Alternative Splicing GalleryENSG00000160221
Gene ExpressionC21orf33 [ NCBI-GEO ]   C21orf33 [ EBI - ARRAY_EXPRESS ]   C21orf33 [ SEEK ]   C21orf33 [ MEM ]
Gene Expression Viewer (FireBrowse)C21orf33 [ Firebrowse - Broad ]
SOURCE (Princeton)Expression in : [Datasets]   [Normal Tissue Atlas]  [carcinoma Classsification]  [NCI60]
BioGPS (Tissue expression)8209
GTEX Portal (Tissue expression)C21orf33
Human Protein AtlasENSG00000160221-C21orf33 [pathology]   [cell]   [tissue]
Protein : pattern, domain, 3D structure
Domain families : Pfam (Sanger)
Domain families : Pfam (NCBI)
Conserved Domain (NCBI)C21orf33
DMDM Disease mutations8209
Blocks (Seattle)C21orf33
Human Protein Atlas [tissue]ENSG00000160221-C21orf33 [tissue]
HPRD09044
Protein Interaction databases
FunCoupENSG00000160221
BioGRIDC21orf33
STRING (EMBL)C21orf33
ZODIACC21orf33
Ontologies - Pathways
Huge Navigator - [HugePedia]
snp3D : Map Gene to Disease8209
BioCentury BCIQC21orf33
ClinGenC21orf33
Clinical trials, drugs, therapy
Chemical/Protein Interactions : CTD8209
Clinical trialC21orf33
Miscellaneous
canSAR (ICR)C21orf33 (select the gene name)
Probes
Litterature
GeneRIFsGene References Into Functions (Entrez)
CoreMineC21orf33
EVEXC21orf33
GoPubMedC21orf33
iHOPC21orf33
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Aug 27 11:12:22 CEST 2018

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