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Ask your administrator if you think this is wrong. ======= SMARCAD1 ======= == Gene Information == * **<color #00a2e8>Official Symbol</color>**: SMARCAD1 * **<color #00a2e8>Official Name</color>**: SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1 * **<color #00a2e8>Aliases and Previous Symbols</color>**: N/A * **<color #00a2e8>Entrez ID</color>**: [[https://www.ncbi.nlm.nih.gov/gene/?term=56916|56916]] * **<color #00a2e8>UniProt</color>**: [[https://www.uniprot.org/uniprot/Q9H4L7|Q9H4L7]] * **<color #00a2e8>Interactions</color>**: [[https://thebiogrid.org/search.php?search=SMARCAD1&organism=9606|BioGRID]] * **<color #00a2e8>PubMed articles</color>**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SMARCAD1|Open PubMed]] * **<color #00a2e8>OMIM</color>**: [[https://omim.org/entry/612761|Open OMIM]] == Function Summary == * **<color #00a2e8>Entrez Summary</color>**: This gene encodes a member of the SNF subfamily of helicase proteins. The encoded protein plays a critical role in the restoration of heterochromatin organization and propagation of epigenetic patterns following DNA replication by mediating histone H3/H4 deacetylation. Mutations in this gene are associated with adermatoglyphia. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]. * **<color #00a2e8>UniProt Summary</color>**: DNA helicase that possesses intrinsic ATP-dependent nucleosome-remodeling activity and is both required for DNA repair and heterochromatin organization. Promotes DNA end resection of double-strand breaks (DSBs) following DNA damage: probably acts by weakening histone DNA interactions in nucleosomes flanking DSBs. Required for the restoration of heterochromatin organization after replication. Acts at replication sites to facilitate the maintenance of heterochromatin by directing H3 and H4 histones deacetylation, H3 'Lys-9' trimethylation (H3K9me3) and restoration of silencing. {ECO:0000269|PubMed:21549307, ECO:0000269|PubMed:22960744}. <button type='primary' size='sm' modal='Pfam_Domains'>Pfam Domains</button> <button type='primary' size='sm' modal='GO_terms'>GO Terms</button> <modal id='Pfam_Domains' size='lg' title='Pfam Domains'> |SNF2 N| |Helicase C| |ResIII| |DEAD| </modal> <modal id='GO_terms' size='lg' title='GO Terms'> |histone H4 deacetylation| |nuclear replication fork| |histone H3 deacetylation| |DNA double-strand break processing| |heterochromatin| |chromosome separation| |DNA-dependent ATPase activity| |histone deacetylation| |protein deacetylation| |site of double-strand break| |DNA helicase activity| |protein deacylation| |macromolecule deacylation| |ATP-dependent chromatin remodeling| |regulation of DNA recombination| |nuclear matrix| |DNA duplex unwinding| |DNA geometric change| |chromatin remodeling| |double-strand break repair| |nucleic acid binding| |chromosome segregation| |DNA conformation change| |protein homooligomerization| |regulation of DNA metabolic process| |histone modification| |covalent chromatin modification| |chromatin binding| |nucleotide metabolic process| |nucleoside phosphate metabolic process| |DNA repair| |protein complex oligomerization| |nucleobase-containing small molecule metabolic process| |chromatin organization| |DNA metabolic process| |cellular response to DNA damage stimulus| |organophosphate metabolic process| |cell cycle process| |chromosome organization| |cell cycle| |DNA binding| |ATP binding| |positive regulation of transcription, DNA-templated| |protein-containing complex assembly| |positive regulation of nucleic acid-templated transcription| |positive regulation of RNA biosynthetic process| |cellular response to stress| |positive regulation of RNA metabolic process| |small molecule metabolic process| |protein-containing complex subunit organization| |positive regulation of nucleobase-containing compound metabolic process| |positive regulation of macromolecule biosynthetic process| |positive regulation of cellular biosynthetic process| |positive regulation of gene expression| |positive regulation of biosynthetic process| </modal> \\ === CRISPR Data === <button type='primary' size='small' modal='Compound_Hit'>Compound Hit</button> <button type='default' size='small' modal='Most_Correlated_Genes'>Most Correlated Genes in Chemogenomics</button> <button type='primary' size='small' modal='Essential_Avana'>Tissues where Essential in the Avana Dataset (DepMap 20Q1)</button> <modal id='Compound_Hit' size='lg' title='Compound Hit'> ^Screen^Score^ |[[:results:exp390|Pifithrin-alpha 20μM R07 exp390]]|-1.84| |[[:results:exp365|I-BRD9 4μM R07 exp365]]|-1.8| |[[:results:exp535|Trimetrexate 0.03μM R08 exp535]]|1.71| |[[:results:exp489|Hippuristanol 0.12μM R08 exp489 no dilution day6]]|1.75| |[[:results:exp463|Caffeine 2600μM R08 exp463]]|2.03| </modal> <modal id='Most_Correlated_Genes' size='lg' title='Most Correlated Genes in Chemogenomics'> No correlation found to any other genes in chemogenomics. </modal> <modal id='Essential_Avana' size='lg' title='Tissues where Essential in the Avana Dataset (DepMap 20Q1)'> Global Fraction of Cell Lines Where Essential: 0/726 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/25| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/15| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/14| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/7| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| </modal> == Essentiality in NALM6 == * **<color #00a2e8>Essentiality Rank</color>**: 18307 * **<color #00a2e8>Expression level (log2 read counts)</color>**: 6.82 <button type='primary' size='small' modal='Dist_expr'>Expression Distribution</button> <modal id='Dist_expr' size='lg' title='SMARCAD1 Expression in NALM6 Cells: 6.82'> {{:chemogenomics:nalm6 dist.png?nolink |}} </modal> Last modified: 2025/12/10 20:19by 127.0.0.1