InnateDB Protein
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IDBP-29962.6
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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SMARCD1
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Protein Name
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SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
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Synonyms
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BAF60A; CRACD1; Rsc6p;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000370924
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InnateDB Gene
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IDBG-32344 (SMARCD1)
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Protein Structure
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Function |
Involved in chromatin remodeling. Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a post-mitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state. The transition from proliferating neural stem/progenitor cells to post-mitotic neurons requires a switch in subunit composition of the npBAF and nBAF complexes. As neural progenitors exit mitosis and differentiate into neurons, npBAF complexes which contain ACTL6A/BAF53A and PHF10/BAF45A, are exchanged for homologous alternative ACTL6B/BAF53B and DPF1/BAF45B or DPF3/BAF45C subunits in neuron-specific complexes (nBAF). The npBAF complex is essential for the self-renewal/proliferative capacity of the multipotent neural stem cells. The nBAF complex along with CREST plays a role regulating the activity of genes essential for dendrite growth (By similarity). Has a strong influence on the Vitamin D-mediated transcriptional activity from an enhancer Vitamin D receptor element (VDRE). May be a link between mammalian SWI-SNF-like chromatin remodeling complexes and the vitamin D receptor (VDR) heterodimer. Mediates critical interactions between nuclear receptors and the BRG1/SMARCA4 chromatin-remodeling complex for transactivation. Also involved in vitamin D-coupled transcription regulation via its association with the WINAC complex, a chromatin-remodeling complex recruited by vitamin D receptor (VDR), which is required for the ligand- bound VDR-mediated transrepression of the CYP27B1 gene. {ECO:0000250, ECO:0000269PubMed:12837248, ECO:0000269PubMed:12917342, ECO:0000269PubMed:14698202, ECO:0000269PubMed:8804307}.
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Subcellular Localization |
Nucleus {ECO:0000269PubMed:8804307, ECO:0000305}.
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Disease Associations |
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Tissue Specificity |
Expressed in all tissues tested, including brain, heart, kidney, liver, lung, muscle, pancreas and placenta. {ECO:0000269PubMed:8804307}.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 100 experimentally validated interaction(s) in this database.
They are also associated with 11 interaction(s) predicted by orthology.
Experimentally validated |
Total |
100
[view]
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Protein-Protein |
100
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Predicted by orthology |
Total |
11 [view]
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR003121
SWIB/MDM2 domain
IPR019835
SWIB domain
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PFAM |
PF02201
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PRINTS |
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PIRSF |
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SMART |
SM00151
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TIGRFAMs |
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Modification |
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SwissProt |
Q96GM5
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PhosphoSite |
PhosphoSite-Q96GM5
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TrEMBL |
F8VW95
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UniProt Splice Variant |
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Entrez Gene |
6602
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UniGene |
Hs.79335
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RefSeq |
NP_620710
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HUGO |
HGNC:11106
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OMIM |
601735
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CCDS |
CCDS8798
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HPRD |
03438
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IMGT |
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EMBL |
AC025154
AF109733
BC009368
CH471111
U66617
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GenPept |
AAC50695
AAD23390
AAH09368
EAW58122
EAW58124
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