what is quaternary gene pool?

PTX3 (Pentraxin 3) is a Protein Coding gene. Gene Ontology (GO) annotations related to this gene include virion binding and (1->3)-beta-D-glucan binding. Gene Ontology (GO) annotations related to this gene include virion binding and (1->3)-beta-D-glucan binding. KEAP1 (Kelch Like ECH Associated Protein 1) is a Protein Coding gene. ACLY (ATP Citrate Lyase) is a Protein Coding gene. Diseases associated with ADIPOQ include Adiponectin, Serum Level Of, Quantitative Trait Locus 1 and Fatty Liver Disease.Among its related pathways are Adipogenesis and AMP-activated protein kinase (AMPK) signaling.Gene Ontology (GO) annotations related to this gene include protein Diseases associated with IFNB1 include Primary Progressive Multiple Sclerosis and Secondary Progressive Multiple Sclerosis.Among its related pathways are Dendritic Cells Developmental Lineage Pathway and Cellular Senescence.Gene Ontology (GO) annotations related to this gene include cytokine activity and TAGLN (Transgelin) is a Protein Coding gene. This gene encodes a protein which belongs to the GATA family of transcription factors. KEAP1 (Kelch Like ECH Associated Protein 1) is a Protein Coding gene. Complete information for SELENOP gene (Protein Coding), Selenoprotein P, including: function, proteins, disorders, pathways, orthologs, and expression. Diseases associated with LRP1 include Keratosis Pilaris Atrophicans and Atrophoderma Vermiculata.Among its related pathways are PDGFR-beta signaling pathway and Familial hyperlipidemia type 1.Gene Ontology (GO) annotations related to this gene include RNA binding and signaling receptor activity. TTN (Titin) is a Protein Coding gene. Among its related pathways are Dendritic Cells Developmental Lineage Pathway and CLEC7A (Dectin-1) signaling. ARG2 (Arginase 2) is a Protein Coding gene. Gene Ontology (GO) annotations related to this gene include arginase activity. ACLY (ATP Citrate Lyase) is a Protein Coding gene. Among its related pathways are Dendritic Cells Developmental Lineage Pathway and CLEC7A (Dectin-1) signaling. PTX3 (Pentraxin 3) is a Protein Coding gene. Diseases associated with MUC1 include Tubulointerstitial Kidney Disease, Autosomal Dominant, 2 and Syringoma.Among its related pathways are CLEC7A (Dectin-1) signaling and Metabolism of proteins.Gene Ontology (GO) annotations related to this gene include RNA polymerase II cis-regulatory region The protein contains two GATA-type zinc fingers and is an important regulator of T-cell development and plays an important role in endothelial cell biology. GeneCards - The Among its related pathways are Lung fibrosis and Innate Immune System. A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele). Diseases associated with ARG2 include Argininemia and Cerebellar Ataxia Type 9. It plays a role in the regulation of macrophage function in host defense through the suppression of anti-inflammatory effects of glucocorticoids. Diseases associated with IFNB1 include Primary Progressive Multiple Sclerosis and Secondary Progressive Multiple Sclerosis.Among its related pathways are Dendritic Cells Developmental Lineage Pathway and Cellular Senescence.Gene Ontology (GO) annotations related to this gene include cytokine activity and Complete information for SELENOP gene (Protein Coding), Selenoprotein P, including: function, proteins, disorders, pathways, orthologs, and expression. Diseases associated with CEBPD include Speech And Communication Disorders and Dysgraphia.Among its related pathways are Adipogenesis and IL-17 Family Signaling Pathways.Gene Ontology (GO) annotations related to this gene include DNA-binding transcription factor activity and RNA polymerase II cis Diseases associated with TTN include Myopathy, Myofibrillar, 9, With Early Respiratory Failure and Salih Myopathy.Among its related pathways are Response to elevated platelet cytosolic Ca2+ and Cardiac conduction.Gene Ontology (GO) annotations related to this gene include nucleic acid binding and identical protein binding. DUSP1 (Dual Specificity Phosphatase 1) is a Protein Coding gene. A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele). A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele). SequenceCaution: CD163 Knockout Pool; CD163 Knockout Cell Line; CD163 CRISPR Edited SNV Cell Line; The protein encoded by this gene is a member of the scavenger receptor cysteine-rich (SRCR) superfamily, and is exclusively expressed in monocytes and macrophages. Among its related pathways are Lung fibrosis and Innate Immune System. This gene encodes a lymphokine involved in cell-mediated immunity, immunoregulation, and inflammation. It plays a role in the regulation of macrophage function in host defense through the suppression of anti-inflammatory effects of glucocorticoids. Diseases associated with LRP1 include Keratosis Pilaris Atrophicans and Atrophoderma Vermiculata.Among its related pathways are PDGFR-beta signaling pathway and Familial hyperlipidemia type 1.Gene Ontology (GO) annotations related to this gene include RNA binding and signaling receptor activity. PTX3 (Pentraxin 3) is a Protein Coding gene. CD209 (CD209 Molecule) is a Protein Coding gene. LRP1 (LDL Receptor Related Protein 1) is a Protein Coding gene. CD209 (CD209 Molecule) is a Protein Coding gene. COL1A1 (Collagen Type I Alpha 1 Chain) is a Protein Coding gene. Diseases associated with TTN include Myopathy, Myofibrillar, 9, With Early Respiratory Failure and Salih Myopathy.Among its related pathways are Response to elevated platelet cytosolic Ca2+ and Cardiac conduction.Gene Ontology (GO) annotations related to this gene include nucleic acid binding and identical protein binding. The protein encoded by this gene is a member of the scavenger receptor cysteine-rich (SRCR) superfamily, and is exclusively expressed in monocytes and macrophages. Diseases associated with ACLY include Trichothiodystrophy 1, Photosensitive and Trigonitis.Among its related pathways are Clear cell renal cell carcinoma pathways and Lipid metabolism pathway.Gene Ontology (GO) annotations related to this gene include obsolete cofactor binding and ATP citrate synthase activity. ADIPOQ (Adiponectin, C1Q And Collagen Domain Containing) is a Protein Coding gene. Diseases associated with DUSP1 include Intellectual Developmental Disorder, X-Linked 108 and Ovarian Cancer.Among its related pathways are ERK Signaling and ATF-2 transcription factor network.Gene Ontology (GO) annotations related to this gene include phosphatase activity and protein Diseases associated with CD209 include Dengue Virus and Human Immunodeficiency Virus Type 1. MUC1 (Mucin 1, Cell Surface Associated) is a Protein Coding gene. Diseases associated with PTX3 include Infectious Myocarditis and Takayasu Arteritis. A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in individuals with two pathogenic alleles, either homozygotes (two copies of the same mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele). Among its related pathways are superpathway of L-citrulline metabolism and Regulation of expression of SLITs and ROBOs. Gene Ontology (GO) annotations related to this gene include arginase activity. Diseases associated with BATF include Prion Disease.Among its related pathways are Cytokine Signaling in Immune system and NF-kappaB Signaling.Gene Ontology (GO) annotations related to this gene include DNA-binding transcription factor activity and sequence-specific DNA binding. BATF (Basic Leucine Zipper ATF-Like Transcription Factor) is a Protein Coding gene. Size: 4128 amino acids Molecular mass: 469089 Da Quaternary structure: DNA-PK is a heterotrimer of PRKDC and the Ku dimer (composed of XRCC6/Ku70 and XRCC5/Ku86) (PubMed:15758953, PubMed:25670504).Formation of this complex may be promoted by interaction with ILF3 (PubMed:9442054).Component of the core long-range non-homologous Diseases associated with ARG2 include Argininemia and Cerebellar Ataxia Type 9. Diseases associated with DUSP1 include Intellectual Developmental Disorder, X-Linked 108 and Ovarian Cancer.Among its related pathways are ERK Signaling and ATF-2 transcription factor network.Gene Ontology (GO) annotations related to this gene include phosphatase activity and protein TAGLN (Transgelin) is a Protein Coding gene. DUSP1 (Dual Specificity Phosphatase 1) is a Protein Coding gene. TAGLN (Transgelin) is a Protein Coding gene. Diseases associated with ELAVL1 include Periampullary Adenocarcinoma and Juvenile Polyposis Syndrome.Among its related pathways are Translational Control and Regulation of activated PAK-2p34 by proteasome mediated degradation.Gene Ontology (GO) annotations related to this gene include nucleic Diseases associated with BATF include Prion Disease.Among its related pathways are Cytokine Signaling in Immune system and NF-kappaB Signaling.Gene Ontology (GO) annotations related to this gene include DNA-binding transcription factor activity and sequence-specific DNA binding. IFNB1 (Interferon Beta 1) is a Protein Coding gene. Diseases associated with DUSP1 include Intellectual Developmental Disorder, X-Linked 108 and Ovarian Cancer.Among its related pathways are ERK Signaling and ATF-2 transcription factor network.Gene Ontology (GO) annotations related to this gene include phosphatase activity and protein Diseases associated with COL1A1 include Caffey Disease and Osteogenesis Imperfecta, Type I.Among its related pathways are Development Endothelin-1/EDNRA transactivation of EGFR and ECM proteoglycans.Gene Ontology (GO) annotations related to this gene include identical protein binding and platelet GeneCards - The Quaternary structure: Interacts with CSNK2B. Among its related pathways are superpathway of L-citrulline metabolism and Regulation of expression of SLITs and ROBOs. This lymphokine and the JAB1 protein form a complex in the cytosol near the peripheral plasma membrane, which may DUSP1 (Dual Specificity Phosphatase 1) is a Protein Coding gene. The protein contains two GATA-type zinc fingers and is an important regulator of T-cell development and plays an important role in endothelial cell biology. Diseases associated with LRP1 include Keratosis Pilaris Atrophicans and Atrophoderma Vermiculata.Among its related pathways are PDGFR-beta signaling pathway and Familial hyperlipidemia type 1.Gene Ontology (GO) annotations related to this gene include RNA binding and signaling receptor activity. IFNB1 (Interferon Beta 1) is a Protein Coding gene. CEBPD (CCAAT Enhancer Binding Protein Delta) is a Protein Coding gene. Diseases associated with ADIPOQ include Adiponectin, Serum Level Of, Quantitative Trait Locus 1 and Fatty Liver Disease.Among its related pathways are Adipogenesis and AMP-activated protein kinase (AMPK) signaling.Gene Ontology (GO) annotations related to this gene include protein TTN (Titin) is a Protein Coding gene. CEBPD (CCAAT Enhancer Binding Protein Delta) is a Protein Coding gene. Diseases associated with TAGLN include Peyronie Disease and Werner Syndrome.Among its related pathways are PDGFR-beta signaling pathway and Burn wound healing.Gene Ontology (GO) annotations related to this gene include actin binding and actin filament binding.An important paralog of this gene is TAGLN3. Size: 4128 amino acids Molecular mass: 469089 Da Quaternary structure: DNA-PK is a heterotrimer of PRKDC and the Ku dimer (composed of XRCC6/Ku70 and XRCC5/Ku86) (PubMed:15758953, PubMed:25670504).Formation of this complex may be promoted by interaction with ILF3 (PubMed:9442054).Component of the core long-range non-homologous

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