SMARCD1 Gene

Name	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
Description	The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and has sequence similarity to the yeast Swp73 protein. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Summary	{"type": "root", "children": [{"type": "p", "children": [{"type": "t", "text": "\nSMARCD1—also known as BAF60a—is a key subunit of the evolutionarily conserved SWI/SNF chromatin remodeling complex that facilitates transcription factor–dependent chromatin remodeling. It directly interacts with nuclear hormone receptors by serving as a molecular bridge, as shown by its engagement with the glucocorticoid receptor even in the absence of the ligand‐binding domain, with the androgen receptor via a specific FxxFF motif, and with melanocyte-specific transcription factors such as MITF to help recruit the BRG1 catalytic subunit for lineage‐specific gene activation."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "1", "end_ref": "3"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nIn the context of cancer biology, SMARCD1 assumes multifaceted roles. Its regulated expression contributes to cellular senescence through both p53‐dependent and independent pathways, and its dysregulation is linked to diverse malignancies. For instance, altered SMARCD1 levels—often modulated by specific microRNAs such as miR‐223 and miR‐99a-5p, or activated by mutant p53—affect tumor growth, chemoresistance, and metastasis in ovarian cancer, hepatocellular carcinoma, head and neck cancers, bladder cancer, melanoma, and breast cancer."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "4", "end_ref": "11"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nBeyond its oncogenic implications, SMARCD1 is essential for proper tissue-specific development and homeostasis. In vascular smooth muscle cells, SMARCD1 promotes inflammatory gene expression and extracellular matrix remodeling, thereby facilitating the formation of abdominal aortic aneurysms. In the nervous system, its activity is required for the transcriptional regulation of genes critical for synaptic circuit formation and long-term memory, while in cardiac tissues, modulation of SMARCD1 influences contractility, Ca²⁺ handling, and overall cardiomyocyte maturation."}, {"type": "fg", "children": [{"type": "fg_fs", "start_ref": "12", "end_ref": "14"}]}, {"type": "t", "text": "\n"}]}, {"type": "t", "text": "\n\n"}, {"type": "p", "children": [{"type": "t", "text": "\nAt a structural and regulatory level, SMARCD1 is integral to the assembly and proper function of the SWI/SNF complex. Its participation in the core subunit assembly underpins chromatin accessibility and gene transcription in various biological processes, including those related to bone and fat metabolism, as genetic studies have linked SMARCD1 polymorphisms to variations in bone mineral density."}, {"type": "fg", "children": [{"type": "fg_f", "ref": "15"}]}, {"type": "t", "text": "\n"}]}, {"type": "rg", "children": [{"type": "r", "ref": 1, "children": [{"type": "t", "text": "Pei-Wen Hsiao, Christy J Fryer, Kevin W Trotter, et al. "}, {"type": "b", "children": [{"type": "t", "text": "BAF60a mediates critical interactions between nuclear receptors and the BRG1 chromatin-remodeling complex for transactivation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Cell Biol (2003)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1128/MCB.23.17.6210-6220.2003"}], "href": "https://doi.org/10.1128/MCB.23.17.6210-6220.2003"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "12917342"}], "href": "https://pubmed.ncbi.nlm.nih.gov/12917342"}]}, {"type": "r", "ref": 2, "children": [{"type": "t", "text": "Dennis J van de Wijngaart, Hendrikus J Dubbink, Michel Molier, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Functional screening of FxxLF-like peptide motifs identifies SMARCD1/BAF60a as an androgen receptor cofactor that modulates TMPRSS2 expression."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Endocrinol (2009)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1210/me.2008-0280"}], "href": "https://doi.org/10.1210/me.2008-0280"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "19762545"}], "href": "https://pubmed.ncbi.nlm.nih.gov/19762545"}]}, {"type": "r", "ref": 3, "children": [{"type": "t", "text": "Shweta Aras, Srinivas Vinod Saladi, Tupa Basuroy, et al. "}, {"type": "b", "children": [{"type": "t", "text": "BAF60A mediates interactions between the microphthalmia-associated transcription factor and the BRG1-containing SWI/SNF complex during melanocyte differentiation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Physiol (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcp.27840"}], "href": "https://doi.org/10.1002/jcp.27840"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30515787"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30515787"}]}, {"type": "r", "ref": 4, "children": [{"type": "t", "text": "Ling He, Ying Chen, Jianguo Feng, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Cellular senescence regulated by SWI/SNF complex subunits through p53/p21 and p16/pRB pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Int J Biochem Cell Biol (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.biocel.2017.07.007"}], "href": "https://doi.org/10.1016/j.biocel.2017.07.007"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "28716547"}], "href": "https://pubmed.ncbi.nlm.nih.gov/28716547"}]}, {"type": "r", "ref": 5, "children": [{"type": "t", "text": "Florence A Arts, Lisa Keogh, Paul Smyth, et al. "}, {"type": "b", "children": [{"type": "t", "text": "miR-223 potentially targets SWI/SNF complex protein SMARCD1 in atypical proliferative serous tumor and high-grade ovarian serous carcinoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Hum Pathol (2017)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.humpath.2017.10.008"}], "href": "https://doi.org/10.1016/j.humpath.2017.10.008"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "29079174"}], "href": "https://pubmed.ncbi.nlm.nih.gov/29079174"}]}, {"type": "r", "ref": 6, "children": [{"type": "t", "text": "Raju S R Adduri, Sara A George, Padmavathi Kavadipula, et al. "}, {"type": "b", "children": [{"type": "t", "text": "SMARCD1 is a transcriptional target of specific non-hotspot mutant p53 forms."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cell Physiol (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/jcp.29332"}], "href": "https://doi.org/10.1002/jcp.29332"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31637714"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31637714"}]}, {"type": "r", "ref": 7, "children": [{"type": "t", "text": "Yongjie Zhou, Qing Xu, Lv Tao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Enhanced SMARCD1, a subunit of the SWI/SNF complex, promotes liver cancer growth through the mTOR pathway."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Clin Sci (Lond) (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1042/CS20200244"}], "href": "https://doi.org/10.1042/CS20200244"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32514535"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32514535"}]}, {"type": "r", "ref": 8, "children": [{"type": "t", "text": "Yihao Zhu, Handong Wang, Maoxing Fei, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Smarcd1 Inhibits the Malignant Phenotypes of Human Glioblastoma Cells via Crosstalk with Notch1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Neurobiol (2021)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s12035-020-02190-z"}], "href": "https://doi.org/10.1007/s12035-020-02190-z"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "33190170"}], "href": "https://pubmed.ncbi.nlm.nih.gov/33190170"}]}, {"type": "r", "ref": 9, "children": [{"type": "t", "text": "Motoki Tamai, Shuichi Tatarano, Shunsuke Okamura, et al. "}, {"type": "b", "children": [{"type": "t", "text": "microRNA-99a-5p induces cellular senescence in gemcitabine-resistant bladder cancer by targeting SMARCD1."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Mol Oncol (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1002/1878-0261.13192"}], "href": "https://doi.org/10.1002/1878-0261.13192"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35148461"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35148461"}]}, {"type": "r", "ref": 10, "children": [{"type": "t", "text": "Jiaoquan Chen, Nanji Yu, Shanshan Ou, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Integrated analysis reveals SMARCD1 is a potential biomarker and therapeutic target in skin cutaneous melanoma."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "J Cancer Res Clin Oncol (2023)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1007/s00432-023-05064-8"}], "href": "https://doi.org/10.1007/s00432-023-05064-8"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "37401939"}], "href": "https://pubmed.ncbi.nlm.nih.gov/37401939"}]}, {"type": "r", "ref": 11, "children": [{"type": "t", "text": "Christina Ross, Li-Yun Gong, Lisa M Jenkins, et al. "}, {"type": "b", "children": [{"type": "t", "text": "SMARCD1 is an essential expression-restricted metastasis modifier."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Commun Biol (2024)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s42003-024-07018-3"}], "href": "https://doi.org/10.1038/s42003-024-07018-3"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "39390150"}], "href": "https://pubmed.ncbi.nlm.nih.gov/39390150"}]}, {"type": "r", "ref": 12, "children": [{"type": "t", "text": "Kevin C J Nixon, Justine Rousseau, Max H Stone, et al. "}, {"type": "b", "children": [{"type": "t", "text": "A Syndromic Neurodevelopmental Disorder Caused by Mutations in SMARCD1, a Core SWI/SNF Subunit Needed for Context-Dependent Neuronal Gene Regulation in Flies."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Am J Hum Genet (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.ajhg.2019.02.001"}], "href": "https://doi.org/10.1016/j.ajhg.2019.02.001"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "30879640"}], "href": "https://pubmed.ncbi.nlm.nih.gov/30879640"}]}, {"type": "r", "ref": 13, "children": [{"type": "t", "text": "Maggie Zi-Ying Chow, Stephanie N Sadrian, Wendy Keung, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Modulation of chromatin remodeling proteins SMYD1 and SMARCD1 promotes contractile function of human pluripotent stem cell-derived ventricular cardiomyocyte in 3D-engineered cardiac tissues."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Sci Rep (2019)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1038/s41598-019-42953-w"}], "href": "https://doi.org/10.1038/s41598-019-42953-w"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "31097748"}], "href": "https://pubmed.ncbi.nlm.nih.gov/31097748"}]}, {"type": "r", "ref": 14, "children": [{"type": "t", "text": "Ziyi Chang, Guizhen Zhao, Yang Zhao, et al. "}, {"type": "b", "children": [{"type": "t", "text": "BAF60a Deficiency in Vascular Smooth Muscle Cells Prevents Abdominal Aortic Aneurysm by Reducing Inflammation and Extracellular Matrix Degradation."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Arterioscler Thromb Vasc Biol (2020)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1161/ATVBAHA.120.314955"}], "href": "https://doi.org/10.1161/ATVBAHA.120.314955"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "32787523"}], "href": "https://pubmed.ncbi.nlm.nih.gov/32787523"}]}, {"type": "r", "ref": 15, "children": [{"type": "t", "text": "Chunming Dong, Rui Zhang, Lijun Xu, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Assembly and interaction of core subunits of BAF complexes and crystal study of the SMARCC1/SMARCE1 binary complex."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "Biochem Biophys Res Commun (2022)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1016/j.bbrc.2022.02.007"}], "href": "https://doi.org/10.1016/j.bbrc.2022.02.007"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "35158202"}], "href": "https://pubmed.ncbi.nlm.nih.gov/35158202"}]}, {"type": "r", "ref": 16, "children": [{"type": "t", "text": "Qiu-Hong Zhou, Lan-Juan Zhao, Ping Wang, et al. "}, {"type": "b", "children": [{"type": "t", "text": "Comprehensive analysis of the association of EGFR, CALM3 and SMARCD1 gene polymorphisms with BMD in Caucasian women."}]}, {"type": "t", "text": " "}, {"type": "i", "children": [{"type": "t", "text": "PLoS One (2014)"}]}, {"type": "t", "text": " DOI: "}, {"type": "a", "children": [{"type": "t", "text": "10.1371/journal.pone.0112358"}], "href": "https://doi.org/10.1371/journal.pone.0112358"}, {"type": "t", "text": " PMID: "}, {"type": "a", "children": [{"type": "t", "text": "25396734"}], "href": "https://pubmed.ncbi.nlm.nih.gov/25396734"}]}]}]}
Synonyms	BAF60A, Rsc6p, CRACD1
Proteins	SMRD1_HUMAN
NCBI Gene ID	6602
API
Download Associations
Predicted Functions
Co-expressed Genes
Expression in Tissues and Cell Lines

Functional Associations

SMARCD1 has 7,267 functional associations with biological entities spanning 9 categories (molecular profile, organism, functional term, phrase or reference, chemical, disease, phenotype or trait, structural feature, cell line, cell type or tissue, gene, protein or microRNA, sequence feature) extracted from 118 datasets.

Click the + buttons to view associations for SMARCD1 from the datasets below.

If available, associations are ranked by standardized value

Harmonizome 3.0

SMARCD1 Gene

Functional Associations

Please acknowledge the Harmonizome in your publications by citing the following reference(s):

	Dataset	Summary
	Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of SMARCD1 gene relative to other tissues from the Allen Brain Atlas Adult Human Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles	tissues with high or low expression of SMARCD1 gene relative to other tissues from the Allen Brain Atlas Adult Mouse Brain Tissue Gene Expression Profiles dataset.
	Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles	tissue samples with high or low expression of SMARCD1 gene relative to other tissue samples from the Allen Brain Atlas Aging Dementia and Traumatic Brain Injury Tissue Sample Gene Expression Profiles dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray	tissue samples with high or low expression of SMARCD1 gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by Microarray dataset.
	Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq	tissue samples with high or low expression of SMARCD1 gene relative to other tissue samples from the Allen Brain Atlas Developing Human Brain Tissue Gene Expression Profiles by RNA-seq dataset.
	Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles	tissues with high or low expression of SMARCD1 gene relative to other tissues from the Allen Brain Atlas Prenatal Human Brain Tissue Gene Expression Profiles dataset.
	Biocarta Pathways	pathways involving SMARCD1 protein from the Biocarta Pathways dataset.
	BioGPS Cell Line Gene Expression Profiles	cell lines with high or low expression of SMARCD1 gene relative to other cell lines from the BioGPS Cell Line Gene Expression Profiles dataset.
	BioGPS Human Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of SMARCD1 gene relative to other cell types and tissues from the BioGPS Human Cell Type and Tissue Gene Expression Profiles dataset.
	BioGPS Mouse Cell Type and Tissue Gene Expression Profiles	cell types and tissues with high or low expression of SMARCD1 gene relative to other cell types and tissues from the BioGPS Mouse Cell Type and Tissue Gene Expression Profiles dataset.
	Carcinogenome Chemical Perturbation Carcinogenicity Signatures	small molecule perturbations changing expression of SMARCD1 gene from the Carcinogenome Chemical Perturbation Carcinogenicity Signatures dataset.
	CCLE Cell Line Gene CNV Profiles	cell lines with high or low copy number of SMARCD1 gene relative to other cell lines from the CCLE Cell Line Gene CNV Profiles dataset.
	CCLE Cell Line Gene Expression Profiles	cell lines with high or low expression of SMARCD1 gene relative to other cell lines from the CCLE Cell Line Gene Expression Profiles dataset.
	CCLE Cell Line Proteomics	Cell lines associated with SMARCD1 protein from the CCLE Cell Line Proteomics dataset.
	CellMarker Gene-Cell Type Associations	cell types associated with SMARCD1 gene from the CellMarker Gene-Cell Type Associations dataset.
	ChEA Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of SMARCD1 gene from the CHEA Transcription Factor Binding Site Profiles dataset.
	ChEA Transcription Factor Targets	transcription factors binding the promoter of SMARCD1 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets dataset.
	ChEA Transcription Factor Targets 2022	transcription factors binding the promoter of SMARCD1 gene in low- or high-throughput transcription factor functional studies from the CHEA Transcription Factor Targets 2022 dataset.
	ClinVar Gene-Phenotype Associations 2025	phenotypes associated with SMARCD1 gene from the curated ClinVar Gene-Phenotype Associations 2025 dataset.
	CM4AI U2OS Cell Map Protein Localization Assemblies	assemblies containing SMARCD1 protein from integrated AP-MS and IF data from the CM4AI U2OS Cell Map Protein Localization Assemblies dataset.
	CMAP Signatures of Differentially Expressed Genes for Small Molecules	small molecule perturbations changing expression of SMARCD1 gene from the CMAP Signatures of Differentially Expressed Genes for Small Molecules dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores	cellular components containing SMARCD1 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores dataset.
	COMPARTMENTS Curated Protein Localization Evidence Scores 2025	cellular components containing SMARCD1 protein from the COMPARTMENTS Curated Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores	cellular components containing SMARCD1 protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores dataset.
	COMPARTMENTS Experimental Protein Localization Evidence Scores 2025	cellular components containing SMARCD1 protein in low- or high-throughput protein localization assays from the COMPARTMENTS Experimental Protein Localization Evidence Scores 2025 dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores	cellular components co-occuring with SMARCD1 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores dataset.
	COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025	cellular components co-occuring with SMARCD1 protein in abstracts of biomedical publications from the COMPARTMENTS Text-mining Protein Localization Evidence Scores 2025 dataset.
	CORUM Protein Complexes	protein complexs containing SMARCD1 protein from the CORUM Protein Complexes dataset.
	COSMIC Cell Line Gene Mutation Profiles	cell lines with SMARCD1 gene mutations from the COSMIC Cell Line Gene Mutation Profiles dataset.
	CTD Gene-Disease Associations	diseases associated with SMARCD1 gene/protein from the curated CTD Gene-Disease Associations dataset.
	DepMap CRISPR Gene Dependency	cell lines with fitness changed by SMARCD1 gene knockdown relative to other cell lines from the DepMap CRISPR Gene Dependency dataset.
	DISEASES Experimental Gene-Disease Association Evidence Scores 2025	diseases associated with SMARCD1 gene in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores 2025 dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores	diseases co-occuring with SMARCD1 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.
	DISEASES Text-mining Gene-Disease Association Evidence Scores 2025	diseases co-occuring with SMARCD1 gene in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores 2025 dataset.
	DisGeNET Gene-Disease Associations	diseases associated with SMARCD1 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.
	DisGeNET Gene-Phenotype Associations	phenotypes associated with SMARCD1 gene in GWAS and other genetic association datasets from the DisGeNET Gene-Phenoptype Associations dataset.
	ENCODE Histone Modification Site Profiles	histone modification site profiles with high histone modification abundance at SMARCD1 gene from the ENCODE Histone Modification Site Profiles dataset.
	ENCODE Transcription Factor Binding Site Profiles	transcription factor binding site profiles with transcription factor binding evidence at the promoter of SMARCD1 gene from the ENCODE Transcription Factor Binding Site Profiles dataset.
	ENCODE Transcription Factor Targets	transcription factors binding the promoter of SMARCD1 gene in ChIP-seq datasets from the ENCODE Transcription Factor Targets dataset.
	ESCAPE Omics Signatures of Genes and Proteins for Stem Cells	PubMedIDs of publications reporting gene signatures containing SMARCD1 from the ESCAPE Omics Signatures of Genes and Proteins for Stem Cells dataset.