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

HMGN4 (high mobility group nucleosomal binding domain 4)

Identity

Other namesHMG17L3
MGC5145
NHC
HGNC HMGN4
Location 6p21.3
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
HGNCHMGN4   4989
Entrez_GeneHMGN4  10473  high mobility group nucleosomal binding domain 4
Cards
GeneCardsHMGN4
EnsemblHMGN4 [Search_View]   ENSG00000182952 [Gene_View]
GenatlasHMGN4
GeneLynxHMGN4
eGenomeHMGN4
euGene10473
Genomic and cartography
GoldenPathHMGN4  -  6p21.3   chr6:26646551-26655143 +  6p22.1   [Description]    (hg18-March_2006)
EnsemblHMGN4 - 6p22.1 [CytoView]
NCBIMapview
HomoloGeneHMGN4
Gene and transcription
GenbankAK311841 [ ENTREZ ]
GenbankAU143224 [ ENTREZ ]
GenbankBC001282 [ ENTREZ ]
GenbankBC035998 [ ENTREZ ]
GenbankBT009824 [ ENTREZ ]
RefSeqNM_006353 [ SRS ]    NM_006353 [ ENTREZ ]
RefSeqAC_000049 [ SRS ]    AC_000049 [ ENTREZ ]
RefSeqAC_000138 [ SRS ]    AC_000138 [ ENTREZ ]
RefSeqNC_000006 [ SRS ]    NC_000006 [ ENTREZ ]
RefSeqNT_007592 [ SRS ]    NT_007592 [ ENTREZ ]
RefSeqNW_001838974 [ SRS ]    NW_001838974 [ ENTREZ ]
RefSeqNW_922984 [ SRS ]    NW_922984 [ ENTREZ ]
AceViewHMGN4 AceView - NCBI
UnigeneHs.236774 [ SRS ]    Hs.236774 [ NCBI ]     HS236774 [ spliceNest ]
Fast-db4555 (alternative variants)
Protein : pattern, domain, 3D structure
SwissProtO00479 [ SRS]    O00479 [ EXPASY ]     O00479 [ INTERPRO ]     O00479 [ UNIPROT ]
PrositePS00355 HMG14_17 [ SRS ]    PS00355 HMG14_17 [ Expasy ]
InterproIPR000079 HMG_14_17 [ SRS ]    IPR000079 HMG_14_17 [ EBI ]
CluSTrO00479
PfamPF01101 HMG14_17 [ SRS ]    PF01101 HMG14_17 [ Sanger ]    pfam01101 [ NCBI-CDD ]
SmartSM00527 HMG17 [EMBL]
BlocksO00479
HPRD17111
Protein Interaction databases
DIPO00479
IntActO00479
Polymorphism : SNP, mutations, diseases
SNPHMGN4 [dbSNP-NCBI]  
SNPNM_006353 [SNP-NCI]  
SNPHMGN4 [GeneSNPs - Utah]  HMGN4] [HGBASE - SRS]
HAPMAPHMGN4 [HAPMAP]  
COSMICHMGN4 [Somatic mutation (COSMIC-CGP-Sanger)]  
HGMDHMGN4
General knowledge
Family BrowserHMGN4 [UCSC Family Browser]
SOURCENM_006353
SMDHs.236774
SAGEHs.236774
GOchromatin [Amigo]  chromatin
GODNA binding [Amigo]  DNA binding
GOnucleus [Amigo]  nucleus
PubGeneHMGN4
TreeFamHMGN4
CTD10473 [Comparative ToxicoGenomics Database]
Other databases
Probes
ProbeHMGN4 Related clones (RZPD - Berlin)
PubMed
PubMed6 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 20:14:26 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.