Paired amphipathic helix protein Sin3a is a protein that in humans is encoded by the SIN3A gene. The protein encoded by this gene is a transcriptional...
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function of switch‐insensitive 3 transcription regulator family member A (SIN3A). The syndrome was discovered by developmental neuroscientists Josefine...
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Sin3A-associated protein, 30kDa, also known as SAP30, is a protein which in humans is encoded by the SAP30 gene. Histone acetylation plays a key role...
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syndrome with or without renal agenesis Noonan syndrome 4 Orofacial cleft 15 SIN3A-related intellectual disability syndrome due to a point mutation Singleton-Merten...
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Renpenning syndrome Seckel syndrome 9 Severe X-linked myotubular myopathy SIN3A-related intellectual disability syndrome due to a point mutation...
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Density 95 RASA1 (RasGAP) Not known Ras GTPase activating protein SH3GL3 Yes Endocytosis SIN3A Yes Transcriptional repressor Sp1 Yes Transcription factor...
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RCOR (REST corepressor) RCOR1 (RCOR1) RCOR2 (RCOR2) RCOR3 (RCOR3) Sin3 SIN3A (SIN3A) SIN3B (SIN3B) TIF1 (transcriptional intermediary factor 1) TRIM24 Tripartite...
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Witteveen-Kolk syndrome is a rare genetic disorder caused by mutation on the SIN3A gene in the long arm of chromosome 15 This disambiguation page lists articles...
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inhibition of the tumor suppressor p53 which then leads to enhanced oncogenesis. SIN3A, a regulator of MYC, that acts to inhibit MYC by deacetylating it, is often...
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to interact with: GATAD2B, HDAC1, Histone deacetylase 2, MBD3 MIZF, and SIN3A. GRCh38: Ensembl release 89: ENSG00000134046 – Ensembl, May 2017 GRCm38:...
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methylated CpG sites on the DNA strands. The TRD region then reacts with SIN3A to recruit histone deacetylases (HDAC). There are also unusual, repetitive...
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SIN3A (MIM 607776) corepressor complex (Fleischer et al., 2003).[supplied by OMIM] SAP130 has been shown to interact with: CSN1S1, CUL2, Myc, SIN3A,...
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357–64. doi:10.1016/S0092-8674(00)80216-0. PMID 9150135. "Entrez Gene: SAP18 Sin3A-associated protein, 18kDa". Michelle L, Cloutier A, Toutant J, Shkreta L...
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and 5) in ~40% of cases one or more of various other genes such as MLL2, SIN3A, ARID1A, EP300, CREBBP, and TBL1XR1) that have chromatin remodeling activity...
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P81133 14799 SIM2 HGNC:10883 Q14190 14800 SIMC1 HGNC:24779 Q8NDZ2 14801 SIN3A HGNC:19353 Q96ST3 14802 SIN3B HGNC:19354 O75182 14803 SINHCAF HGNC:30702...
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gene and contain binding sites for transcription factors RCOR1, MILLT1, SIN3A, NFIC, STAT3, JUNB, FOS, EGR1, PHB2, RUNX3, and SRF. Many of these transcription...
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These complexes include Sin3 (named after its characteristic protein mSin3A), Nucleosome Remodelling and Deacetylating complex (NuRD), and Co-REST....
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CREBBP, CCNE1, ESR1, FANCA, HSP90B1, ING1, Myc, NR3C1, P53, POLR2A, PHB, SIN3A, SMARCB1, SMARCC1, SMARCC2, SMARCE1, STAT2, and STK11. GRCh38: Ensembl release...
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been shown to interact with: ACTL6A, ARID1B, CEBPB, POLR2A, Prohibitin, SIN3A, SMARCB1, SMARCC1, and SS18. - Nicolaides Baraitser Syndrome (NCBRS) GRCh38:...
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a subunit of the histone deacetylase (see HDAC1; MIM 601241)-dependent SIN3A (MIM 607776) corepressor complex (Fleischer et al., 2003).[supplied by OMIM]...
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humans is encoded by the PHF12 gene. PHF12 has been shown to interact with SIN3A. GRCh38: Ensembl release 89: ENSG00000109118 – Ensembl, May 2017 GRCm38:...
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a co-repressor complex to promote histone deacetylation upon binding to SIN3A. SUMOylation refers to the addition of Small Ubiquitin-like Modifier (SUMO)...
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DePinho RA, Dejean A (May 1998). "Histone deacetylase associated with mSin3A mediates repression by the acute promyelocytic leukemia-associated PLZF...
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(April 2001). "PSF is a novel corepressor that mediates its effect through Sin3A and the DNA binding domain of nuclear hormone receptors". Molecular and...
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Retinoblastoma-like protein 1, Retinoblastoma-like protein 2, SAP30, SATB1, SIN3A, SIN3B, SPEN, SUDS3, SUV39H1, Sp1 transcription factor, TOP2A, TOP2B, and...
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with: BAP1, CREB3, GABPA, HDAC1, HDAC2, MLL, OGT, PDCD2, POU2F1, PPP1CA, SIN3A, SP1, SUDS3, WDR5, and ZBTB17. GRCh38: Ensembl release 89: ENSG00000172534...
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to interact with NFKB1, RELA, RELB, BTRC, RPS27A, BCL3, MAP3K8, NFKBIA, SIN3A, SUMO1, Tat. Mutations in the TANGO2 gene may cause defects in mitochondrial...
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activity via interaction with the common transcriptional co-repressor, Sin3A. KLFs 15 and 17 are distantly related without any defined protein interaction...
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Histone H2B, AKT1, PFKL, KMT2E/MLL5, MAPT/TAU, Host cell factor C1, and SIN3A. O-GlcNAc transferase is a part of a host of biological functions within...
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The encoded protein is a subunit of the histone deacetylase-dependent SIN3A transcriptional corepressor complex, which functions in diverse cellular...
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