Atlas of Genetics and Cytogenetics in Oncology and Haematology


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RNF17 (ring finger protein 17)

Identity

Other namesFLJ11045
Mmip-2
SPATA23
TDRD4
HGNC RNF17
Location 13q12.13
Location_base_pair Starts at 24236301 and ends at 24352058 bp from pter ( according to hg18-March_2006).
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
HGNCRNF17   10060
Entrez_GeneRNF17  56163  ring finger protein 17
Cards
GeneCardsRNF17
EnsemblRNF17 [Search_View]   ENSG00000132972 [Gene_View]
GenatlasRNF17
GeneLynxRNF17
eGenomeRNF17
euGene56163
Genomic and cartography
GoldenPathRNF17  -  13q12.13   chr13:24236301-24352058 +  13q12.12   [Description]    (hg18-March_2006)
EnsemblRNF17 - 13q12.12 [CytoView]
NCBIMapview
OMIMDisease map [OMIM]
HomoloGeneRNF17
Gene and transcription
GenbankAF285602 [ ENTREZ ]
GenbankAF285603 [ ENTREZ ]
GenbankAK001907 [ ENTREZ ]
GenbankBC064847 [ ENTREZ ]
GenbankBC146822 [ ENTREZ ]
RefSeqNM_031277 [ SRS ]    NM_031277 [ ENTREZ ]
RefSeqAC_000056 [ SRS ]    AC_000056 [ ENTREZ ]
RefSeqAC_000145 [ SRS ]    AC_000145 [ ENTREZ ]
RefSeqNC_000013 [ SRS ]    NC_000013 [ ENTREZ ]
RefSeqNT_024524 [ SRS ]    NT_024524 [ ENTREZ ]
RefSeqNW_001838070 [ SRS ]    NW_001838070 [ ENTREZ ]
RefSeqNW_925473 [ SRS ]    NW_925473 [ ENTREZ ]
AceViewRNF17 AceView - NCBI
UnigeneHs.97464 [ SRS ]    Hs.97464 [ NCBI ]     HS97464 [ spliceNest ]
Fast-db1181 (alternative variants)
Protein : pattern, domain, 3D structure
SwissProtQ5T2J8 [ SRS]    Q5T2J8 [ EXPASY ]     Q5T2J8 [ INTERPRO ]     Q5T2J8 [ UNIPROT ]
PrositePS50304 TUDOR [ SRS ]    PS50304 TUDOR [ Expasy ]
InterproIPR008191 Maternal_tudor [ SRS ]    IPR008191 Maternal_tudor [ EBI ]
InterproIPR002999 Tudor [ SRS ]    IPR002999 Tudor [ EBI ]
CluSTrQ5T2J8
PfamPF00567 TUDOR [ SRS ]    PF00567 TUDOR [ Sanger ]    pfam00567 [ NCBI-CDD ]
SmartSM00333 TUDOR [EMBL]
BlocksQ5T2J8
HPRD05779
Protein Interaction databases
DIPQ5T2J8
IntActQ5T2J8
Polymorphism : SNP, mutations, diseases
OMIM605793    [ map ]   
GENECLINICS605793
SNPRNF17 [dbSNP-NCBI]  
SNPNM_031277 [SNP-NCI]  
SNPRNF17 [GeneSNPs - Utah]  RNF17] [HGBASE - SRS]
HAPMAPRNF17 [HAPMAP]  
COSMICRNF17 [Somatic mutation (COSMIC-CGP-Sanger)]  
HGMDRNF17
General knowledge
Family BrowserRNF17 [UCSC Family Browser]
SOURCENM_031277
SMDHs.97464
SAGEHs.97464
GOnucleic acid binding [Amigo]  nucleic acid binding
GOprotein binding [Amigo]  protein binding
GOnucleus [Amigo]  nucleus
GOcytoplasm [Amigo]  cytoplasm
GOmulticellular organismal development [Amigo]  multicellular organismal development
GOspermatogenesis [Amigo]  spermatogenesis
GOzinc ion binding [Amigo]  zinc ion binding
GOhydrolase activity, acting on ester bonds [Amigo]  hydrolase activity, acting on ester bonds
GOcell differentiation [Amigo]  cell differentiation
GOmetal ion binding [Amigo]  metal ion binding
PubGeneRNF17
TreeFamRNF17
CTD56163 [Comparative ToxicoGenomics Database]
Other databases
Probes
ProbeRNF17 Related clones (RZPD - Berlin)
PubMed
PubMed4 Pubmed reference(s) in Entrez
Genes in titleautomatic search in PubMed
REVIEW articlesautomatic search in PubMed
Last year publicationsautomatic search in PubMed

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Contributor(s)

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

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Tue Oct 14 20:52:44 2008


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