Homo sapiens Protein: HMG20B
Summary
InnateDB Protein IDBP-17412.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol HMG20B
Protein Name high mobility group 20B
Synonyms BRAF25; BRAF35; HMGX2; HMGXB2; PP7706; pp8857; SMARCE1r; SOXL;
Species Homo sapiens
Ensembl Protein ENSP00000328269
InnateDB Gene IDBG-17410 (HMG20B)
Protein Structure
UniProt Annotation
Function Required for correct progression through G2 phase of the cell cycle and entry into mitosis. Required for RCOR1/CoREST mediated repression of neuronal specific gene promoters.
Subcellular Localization Nucleus. Chromosome. Note=Localized to condensed chromosomes in mitosis in conjunction with BRCA2.
Disease Associations
Tissue Specificity Ubiquitously expressed in adult tissues. {ECO:0000269PubMed:10773667, ECO:0000269PubMed:11997092}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 32 experimentally validated interaction(s) in this database.
They are also associated with 2 interaction(s) predicted by orthology.
Experimentally validated
Total 32 [view]
Protein-Protein 32 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 2 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0005515 protein binding
GO:0046982 protein heterodimerization activity
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0007049 cell cycle
GO:0007596 blood coagulation
GO:0016568 chromatin modification
GO:0033234 negative regulation of protein sumoylation
GO:0035914 skeletal muscle cell differentiation
GO:0045666 positive regulation of neuron differentiation
Cellular Component
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005694 chromosome
Protein Structure and Domains
PDB ID
InterPro IPR009071 High mobility group box domain
PFAM PF00505
PF09011
PRINTS
PIRSF
SMART SM00398
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9P0W2
PhosphoSite PhosphoSite-Q9P0W2
TrEMBL C9JQA7
UniProt Splice Variant
Entrez Gene 10362
UniGene Hs.406534
RefSeq NP_006330
HUGO HGNC:5002
OMIM 605535
CCDS CCDS45919
HPRD 05703
IMGT
EMBL AC005786 AC116968 AF072165 AF072836 AF146223 AF288679 AF331191 AK090733 AL355709 BC002552 BC003505 BC004408 BC021585 CH471139 CR456754
GenPept AAC26860 AAC62837 AAF66707 AAF76253 AAG01174 AAG60060 AAH02552 AAH03505 AAH04408 AAH21585 BAC03510 CAB90809 CAG33035 EAW69306 EAW69307 EAW69308