Gene Gene information from NCBI Gene database.
Entrez ID 6603
Gene name SWI/SNF related BAF chromatin remodeling complex subunit D2
Gene symbol SMARCD2
Synonyms (NCBI Gene)
BAF60BCRACD2PRO2451Rsc6pSGD2
Chromosome 17
Chromosome location 17q23.3
Summary 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. T
SNPs SNP information provided by dbSNP.
4
SNP ID Visualize variation Clinical significance Consequence
rs112986541 C>G,T Likely-pathogenic Splice acceptor variant
rs1057518731 C>T Pathogenic Splice donor variant
rs1057518733 A>G Pathogenic Splice donor variant
rs1555580263 ->AGGTAGAACCTTATCTGCCATCTTC Pathogenic Stop gained, coding sequence variant, inframe indel
miRNA miRNA information provided by mirtarbase database.
292
miRTarBase ID miRNA Experiments Reference
MIRT004999 hsa-miR-125b-5p Microarray 17891175
MIRT020668 hsa-miR-155-5p Proteomics 18668040
MIRT049267 hsa-miR-92a-3p CLASH 23622248
MIRT049267 hsa-miR-92a-3p CLASH 23622248
MIRT043231 hsa-miR-324-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
38
GO ID Ontology Definition Evidence Reference
GO:0000776 Component Kinetochore NAS 11078522
GO:0000785 Component Chromatin HDA 16217013
GO:0000785 Component Chromatin NAS 12192000
GO:0003712 Function Transcription coregulator activity IBA
GO:0003713 Function Transcription coactivator activity NAS 8804307
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601736 11107 ENSG00000108604
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q92925
Protein name SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 2 (60 kDa BRG-1/Brm-associated factor subunit B) (BRG1-associated factor 60B) (BAF60B)
Protein function Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Component of SWI/SNF chromatin remodeling complexes that carry out key enzymatic activities, changing chromati
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02201 SWIB 309 381 SWIB/MDM2 domain Domain
Tissue specificity TISSUE SPECIFICITY: Isoform 2 is expressed in the pancreas. {ECO:0000269|PubMed:8804307}.
Sequence
MSGRGAGGFPLPPLSPGGGAVAAALGAPPPPAGPGMLPGPALRGPGPAGGVGGPGAAAFR
PMGPAGPAAQYQRPGMSPGNRMPMAGLQVGPPAGSPFGAAAPLRPGMPPTMMDPFRKRLL
VPQAQPPMPAQRRGLKRRKMADKVLPQRIRELVPESQAYMDLLAFERKLDQTIARKRMEI
QEAIKKPLTQKRKLRIYISNTFSPSKAEGDSAGTAGTPGGTPAGDKVASWELRVEGKLLD
DPSKQKRKFSSFFKSLVIELDKELYGPDNHLVEWHRMPTTQETDGFQVKRPGDLNVKCTL
LLMLDHQPPQYKLDPRLARLLGVHTQTRAAIMQALWLYIKHNQLQDGHEREYINCNRYFR
QIFSCGRLRFSEIPMKLAGLL
QHPDPIVINHVISVDPNDQKKTACYDIDVEVDDPLKAQM
SNFLASTTNQQEIASLDVKIHETIESINQLKTQRDFMLSFSTDPQDFIQEWLRSQRRDLK
IITDVIGNPEEERRAAFYHQPWAQEAVGRHIFAKVQQRRQELEQVLGIRLT
Sequence length 531
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  ATP-dependent chromatin remodeling
Thermogenesis
Hepatocellular carcinoma
  RMTs methylate histone arginines
RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
40
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Autosomal recessive severe congenital neutropenia Pathogenic rs1057518731, rs1555580263, rs1057518733 RCV000415510
RCV000415478
RCV000415497
SMARCD2-related disorder Likely pathogenic; Pathogenic rs758123382 RCV003399062
Specific granule deficiency 1 Pathogenic rs1057518731, rs1555580263, rs1057518733 RCV000415510
RCV000415478
RCV000415497
Specific granule deficiency 2 Pathogenic; Likely pathogenic rs1567760022, rs2144630306, rs2144633398, rs2040280183, rs1057518731, rs1555580263, rs1057518733, rs112986541, rs758123382 RCV001844400
RCV001783782
RCV002248346
RCV003337985
RCV000490556
RCV000490559
RCV000490561
RCV000991401
RCV001537635
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Lung cancer Likely benign rs184956592 RCV005912788
Ovarian serous cystadenocarcinoma Benign rs114449005 RCV005914416
Premature ovarian insufficiency Conflicting classifications of pathogenicity rs1379892630 RCV000766170
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Anxiety Separation Associate 33279574
Failure to Thrive Associate 33279574
Leukemia Myeloid Acute Associate 29483235
Sepsis Associate 33279574