2024 Phf21a gene

Phf21a gene

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August undefined, 2024

WebAliases. PHF21A, BHC80, BM-006, PHD finger protein 21A, NEDMS, IDDBCS. External IDs. OMIM: 608325 MGI: 2384756 HomoloGene: 9597 GeneCards: PHF21A. Gene location ( …

51317 - Gene ResultPHF21A PHD finger protein 21A

WebThe .gov means it's official. Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site. WebJan 27, 2024 · Potocki–Shaffer syndrome is a contiguous gene deletion syndrome involving 11p11.2p12 and characterized by multiple exostoses, biparietal foramina, genitourinary anomalies in males, central... thibault azoulay

PHF21A gene - MedlinePlus

WebNov 28, 2024 · e Structure of the PHF21A gene. Vertical and horizontal lines indicate exons and introns, respectively. Vertical filled boxes: protein-coding regions; unfilled boxes: … WebPHF21A (PHD finger protein 21A) is a component of the BHC complex, a corepressor complex that represses transcription of neuron-specific genes in non-neuronal cells. The BHC complex is recruited at RE1/NRSE sites by REST and acts by deacetylating and demethylating specific sites on histones, thereby acting as a chromatin modifier. WebThe gene view histogram is a graphical view of mutations across PHF21A. These mutations are displayed at the amino acid level across the full length of the gene by default. Restrict the view to a region of the gene by dragging across the histogram to highlight the region of interest, or by using the sliders in the filters panel to the left. sage orbot and cubot

Human Gene ZMYM2 (ENST00000382874.6) from GENCODE V43

WikiGenes - PHF21A - PHD finger protein 21A

WebOct 22, 2024 · gest that PHF21A is a contributory gene for these clin-ical features in PSS. The extra C-terminal aberrant tail in the elongated. proteins from patients 1, 3, and 7 could act dominant. WebPHF21A is part of cluster 76 Brain & Bone marrow - Chromatin organization with confidence i Confidence is the fraction of times a gene was assigned to the cluster in repeated clustering, and therefore reflects how strongly associated it is to the cluster. sage oral care brochureWebThe PHF21A gene encodes BHC80, a component of a BRAF35 (MIM 605535)/histone deacetylase (HDAC; see MIM 601241) complex (BHC) that mediates repression of neuron-specific genes through the cis-regulatory element known as repressor element-1 (RE1) or neural restrictive silencer (NRS) (Hakimi et al., 2002 [PubMed 12032298]).[supplied by … thibault baldinger

"WebPHD finger protein 21A is a protein that in humans is encoded by the PHF21A gene.[5][6][7] For faster navigation, this Iframe is preloading the Wikiwand page for PHF21A . Home " - Phf21a gene

Phf21a gene

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Webwikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins ... High impact information on PHF21A; Biological context of PHF21A; Anatomical context of PHF21A; Other interactions of PHF21A; About. … WebThe PHF21A gene encodes BHC80, a component of a BRAF35 (MIM 605535)/histone deacetylase (HDAC; see MIM 601241) complex (BHC) that mediates repression of …

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WebPost-translational modifications of histone variant H2A.Z accompany gene transactivation, but its modifying enzymes still remain elusive. Here, we reveal a hitherto unknown function of human KAT2A ... WebThe PHF21A gene encodes BHC80, a component of a BRAF35 (MIM 605535)/histone deacetylase (HDAC; see MIM 601241) complex (BHC) that mediates repression of neuron …

WebSep 26, 2024 · Phf21a PHD finger protein 21A [ (house mouse)] Gene ID: 192285, updated on 26-Sep-2024 Summary Enables chromatin binding activity. Acts upstream of or within suckling behavior. Located in nucleus. Is expressed in several structures, including central nervous system; cranium; early conceptus; genitourinary system; and hemolymphoid … WebThe ALX4 gene provides instructions for making a member of the homeobox protein family. Homeobox proteins direct the formation of body structures during early embryonic development. The ALX4 protein is necessary for normal development of the skull and formation of the head and face, which begins early in fetal development.

WebMar 21, 2024 · PHF21A. PHD finger protein 21A. Gene ID: 51317, updated on 28-Apr-2024. Gene type: protein coding. Also known as: BHC80; NEDMS; BM-006; IDDBCS. See all … WebView Gene Families for PHF21A_TARGET_GENES. The following table provides a functional overview of the MSigDB gene sets by categorizing their genes into a small number of carefully chosen "gene families". To categorize the genes in a gene set, use the gene set page or the Investigate Gene Sets page.

WebPHF21A Gene, Drug Resistance, Tissue Distribution, Mutation Distribution, Variants, PHF21A Genome Browser, PHF21A References PHF21A - Explore an overview of PHF21A, with a …

WebJul 13, 2012 · PHF21A encodes a plant homeodomain finger protein whose murine and zebrafish orthologs are both expressed in a manner consistent with a function in neurofacial and craniofacial development, and suppression of the latter led to both craniofacial abnormalities and neuronal apoptosis. sage oracle touch ukWebFeb 17, 2024 · Results: Five genes, namely, NOX1, ACVR1B, PHF21A, FTL, and GALNT14, were identified from 10 differentially expressed ferroptosis-related genes to construct a PCOS diagnostic model. Finally, a ceRNA network including 117 lncRNAs, 67 miRNAs, and five ferroptosis-related genes was constructed. thibault badinWebThe PHF21A gene encodes BHC80, a component of a BRAF35 (MIM 605535)/histone deacetylase (HDAC; see MIM 601241) complex (BHC) that mediates repression of neuron … thibault baheuxWebNov 27, 2024 · People who have mutations in a gene called PHF21A tend to have a constellation of traits and conditions, including autism, according to a new study 1. … sage oral care systemWebDec 30, 2024 · Kim et al. (2012) identified 3 patients with balanced translocations disrupting the PHF21A ( 608325) gene in the PSS critical region. The patients had intellectual disability and craniofacial anomalies seen in PSS but did not have other manifestations of the contiguous gene deletion syndrome. thibault baillyWebDec 17, 2024 · PHF21A(PHD finger protein 21A) gene, located in the short arm of chromosome 11, encodes for BHC80, a component of the Lysine Specific Demethylase 1, … sage oracle vs oracle touchWebA Biblioteca Virtual em Saúde é uma colecao de fontes de informacao científica e técnica em saúde organizada e armazenada em formato eletrônico nos países da Região Latino-Americana e do Caribe, acessíveis de forma universal na Internet de modo compatível com as bases internacionais. thibault baert