BRD9
Bromodomain-containing protein 9
Also known as: BRD9_HUMAN, FLJ13441, SMARCI2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H8M2
- Gene
- BRD9
- Ensembl
- ENSG00000028310
- Chromosome
- 5
- Canonical length
- 597 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Enables lysine-acetylated histone binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Located in nucleoplasm. Part of SWI/SNF complex. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
597 residues, UniProt reviewed canonical sequence.
>Q9H8M2|BRD9
1 MGKKHKKHKA EWRSSYEDYA DKPLEKPLKL VLKVGGSEVT ELSGSGHDSS YYDDRSDHER
61 ERHKEKKKKK KKKSEKEKHL DDEERRKRKE EKKRKREREH CDTEGEADDF DPGKKVEVEP
121 PPDRPVRACR TQPAENESTP IQQLLEHFLR QLQRKDPHGF FAFPVTDAIA PGYSMIIKHP
181 MDFGTMKDKI VANEYKSVTE FKADFKLMCD NAMTYNRPDT VYYKLAKKIL HAGFKMMSKQ
241 AALLGNEDTA VEEPVPEVVP VQVETAKKSK KPSREVISCM FEPEGNACSL TDSTAEEHVL
301 ALVEHAADEA RDRINRFLPG GKMGYLKRNG DGSLLYSVVN TAEPDADEEE THPVDLSSLS
361 SKLLPGFTTL GFKDERRNKV TFLSSATTAL SMQNNSVFGD LKSDEMELLY SAYGDETGVQ
421 CALSLQEFVK DAGSYSKKVV DDLLDQITGG DHSRTLFQLK QRRNVPMKPP DEAKVGDTLG
481 DSSSSVLEFM SMKSYPDVSV DISMLSSLGK VKKELDPDDS HLNLDETTKL LQDLHEAQAE
541 RGGSRPSSNL SSLSNASERD QHHLGSPSRL SVGEQPDVTH DPYEFLQSPE PAASAKTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against BRD9 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)
- 0.57
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 17 nTPM
- cerebral cortex: 14 nTPM
- basal ganglia: 14 nTPM
- midbrain: 13 nTPM
- amygdala: 13 nTPM
- choroid plexus: 13 nTPM
Single-cell type
- early spermatids: 197 nCPM
- corticotrophs: 124 nCPM
- late spermatids: 105 nCPM
- somatotrophs: 86 nCPM
- endometrial stromal cells: 79 nCPM
- thyrotrophs: 77 nCPM
Immune cell
- basophil: 7.1 nTPM
- naive B-cell: 6.1 nTPM
- T-reg: 5.2 nTPM
- memory B-cell: 4.9 nTPM
- memory CD8 T-cell: 4.5 nTPM
- memory CD4 T-cell: 4.2 nTPM
Brain region
- medulla oblongata: 20 nTPM
- thalamus: 20 nTPM
- cerebral cortex: 19 nTPM
- white matter: 18 nTPM
- amygdala: 18 nTPM
- basal ganglia: 18 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)
- 0.52
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 1.26
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 14% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chromatin remodeling
- double-strand break repair via homologous recombination
- negative regulation of cell differentiation
- positive regulation of cell population proliferation
- positive regulation of stem cell population maintenance
- regulation of transcription by RNA polymerase II
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of BRD9 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 BRD9 as an antibody target. Whether an autoantibody or antibody against BRD9 could matter depends on whether native BRD9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
BRD9 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 BRD9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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