Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

C21orf33 (chromosome 21 open reading frame 33)

Identity

Other namesD21S2048E
ES1
GT335
HES1
KNP-I
KNPH
KNPI
HGNC C21orf33
Location 21q22.3
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
HGNCC21orf33   1273
Entrez_GeneC21orf33  8209  chromosome 21 open reading frame 33
Cards
GeneCardsC21orf33
EnsemblC21orf33 [Search_View]   ENSG00000160221 [Gene_View]
GenatlasC21orf33
GeneLynxC21orf33
eGenomeC21orf33
euGene8209
Genomic and cartography
GoldenPathC21orf33  -  21q22.3   chr21:44377922-44390033 +  21q22.3   [Description]    (hg18-March_2006)
EnsemblC21orf33 - 21q22.3 [CytoView]
NCBIMapview
OMIMDisease map [OMIM]
HomoloGeneC21orf33
Gene and transcription
GenbankAA045757 [ ENTREZ ]
GenbankBC002370 [ ENTREZ ]
GenbankBC003587 [ ENTREZ ]
GenbankCR595541 [ ENTREZ ]
GenbankCR597695 [ ENTREZ ]
RefSeqNM_004649 [ SRS ]    NM_004649 [ ENTREZ ]
RefSeqNM_198155 [ SRS ]    NM_198155 [ ENTREZ ]
RefSeqAC_000064 [ SRS ]    AC_000064 [ ENTREZ ]
RefSeqAC_000153 [ SRS ]    AC_000153 [ ENTREZ ]
RefSeqNC_000021 [ SRS ]    NC_000021 [ ENTREZ ]
RefSeqNT_011515 [ SRS ]    NT_011515 [ ENTREZ ]
RefSeqNW_001838716 [ SRS ]    NW_001838716 [ ENTREZ ]
RefSeqNW_927384 [ SRS ]    NW_927384 [ ENTREZ ]
AceViewC21orf33 AceView - NCBI
UnigeneHs.413482 [ SRS ]    Hs.413482 [ NCBI ]     HS413482 [ spliceNest ]
Fast-db3884 (alternative variants)
Protein : pattern, domain, 3D structure
SwissProtP30042 [ SRS]    P30042 [ EXPASY ]     P30042 [ INTERPRO ]     P30042 [ UNIPROT ]
InterproIPR002818 ThiJ/PfpI [ SRS ]    IPR002818 ThiJ/PfpI [ EBI ]
CluSTrP30042
PfamPF01965 DJ-1_PfpI [ SRS ]    PF01965 DJ-1_PfpI [ Sanger ]    pfam01965 [ NCBI-CDD ]
BlocksP30042
HPRD09044
Protein Interaction databases
DIPP30042
IntActP30042
Polymorphism : SNP, mutations, diseases
OMIM601659    [ map ]   
GENECLINICS601659
SNPC21orf33 [dbSNP-NCBI]  
SNPNM_004649 [SNP-NCI]  
SNPNM_198155 [SNP-NCI]  
SNPC21orf33 [GeneSNPs - Utah]  C21orf33] [HGBASE - SRS]
HAPMAPC21orf33 [HAPMAP]  
HGMDC21orf33
General knowledge
Family BrowserC21orf33 [UCSC Family Browser]
SOURCENM_004649
SOURCENM_198155
SMDHs.413482
SAGEHs.413482
GOmitochondrion [Amigo]  mitochondrion
PubGeneC21orf33
TreeFamC21orf33
CTD8209 [Comparative ToxicoGenomics Database]
Other databases
Probes
ProbeC21orf33 Related clones (RZPD - Berlin)
PubMed
PubMed13 Pubmed reference(s) in LocusLink
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

Search in all EBI   NCBI

Contributor(s)

Written09-2002Dessen P, Le Minor S
Updated03-2008Dessen P

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon Aug 11 20:02:42 2008


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

j.l.huret@chu-poitiers.fr.