SMARCD3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3
Also known as: BAF60C, CRACD3, Rsc6p, SMRD3_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6STE5
- Gene
- SMARCD3
- Ensembl
- ENSG00000082014
- Chromosome
- 7
- Canonical length
- 483 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
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. Multiple alternatively spliced transcript variants have been found for this gene, but the biological validity of some variants has not been determined. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
483 residues, UniProt reviewed canonical sequence.
>Q6STE5|SMARCD3
1 MAADEVAGGA RKATKSKLFE FLVHGVRPGM PSGARMPHQG APMGPPGSPY MGSPAVRPGL
61 APAGMEPARK RAAPPPGQSQ AQSQGQPVPT APARSRSAKR RKMADKILPQ RIRELVPESQ
121 AYMDLLAFER KLDQTIMRKR VDIQEALKRP MKQKRKLRLY ISNTFNPAKP DAEDSDGSIA
181 SWELRVEGKL LDDPSKQKRK FSSFFKSLVI ELDKDLYGPD NHLVEWHRTP TTQETDGFQV
241 KRPGDLSVRC TLLLMLDYQP PQFKLDPRLA RLLGLHTQSR SAIVQALWQY VKTNRLQDSH
301 DKEYINGDKY FQQIFDCPRL KFSEIPQRLT ALLLPPDPIV INHVISVDPS DQKKTACYDI
361 DVEVEEPLKG QMSSFLLSTA NQQEISALDS KIHETIESIN QLKIQRDFML SFSRDPKGYV
421 QDLLRSQSRD LKVMTDVAGN PEEERRAEFY HQPWSQEAVS RYFYCKIQQR RQELEQSLVV
481 RNTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SMARCD3 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.44
- Highest tissue expression
- 149 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 149 nTPM
- cerebral cortex: 142 nTPM
- amygdala: 128 nTPM
- skeletal muscle: 121 nTPM
- hypothalamus: 91 nTPM
- hippocampal formation: 88 nTPM
Single-cell type
- breast lactating cells: 160 nCPM
- myonuclei: 136 nCPM
- vascular smooth muscle cells: 121 nCPM
- neutrophils: 107 nCPM
- peritubular myoid cells: 107 nCPM
- pericytes: 88 nCPM
Immune cell
- classical monocyte: 5.5 nTPM
- neutrophil: 1.9 nTPM
- myeloid DC: 1.6 nTPM
- intermediate monocyte: 1.3 nTPM
- total PBMC: 1.3 nTPM
- memory CD4 T-cell: 0.5 nTPM
Brain region
- cerebral cortex: 116 nTPM
- basal ganglia: 114 nTPM
- hypothalamus: 106 nTPM
- amygdala: 98 nTPM
- midbrain: 88 nTPM
- thalamus: 88 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.47
- gnomAD pLI
- 0.4
- gnomAD missense Z
- 2.58
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cardiac right ventricle formation
- chromatin remodeling
- muscle cell differentiation
- nervous system development
- neural retina development
- nucleosome disassembly
- positive regulation of cell differentiation
- positive regulation of DNA-templated transcription
- positive regulation of double-strand break repair
- positive regulation of G2/M transition of mitotic cell cycle
- positive regulation of myoblast differentiation
- positive regulation of neuroblast proliferation
- positive regulation of smooth muscle cell differentiation
- positive regulation of T cell differentiation
- regulation of G0 to G1 transition
- regulation of G1/S transition of mitotic cell cycle
- regulation of mitotic metaphase/anaphase transition
- regulation of nucleotide-excision repair
- regulation of transcription by RNA polymerase II
- secondary heart field specification
Molecular functions
- chromatin binding
- DNA-binding transcription factor binding
- nuclear receptor binding
- signaling receptor binding
- transcription coactivator activity
- transcription coregulator activity
- transcription coregulator binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
- SWIB/MDM2 domain
- SWIB domain
- SWIB/MDM2 domain superfamily
- SWIB/MDM2 domain
- SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D 3, SWIB domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SMARCD3 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SMARCD3 as an antibody target. Whether an autoantibody or antibody against SMARCD3 could matter depends on whether native SMARCD3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SMARCD3 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SMARCD3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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