ACTG2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | ACTG2 , ACT, ACTA3, ACTE, ACTL3, ACTSG, VSCM, actin, gamma 2, smooth muscle, enteric, actin gamma 2, smooth muscle, VSCM1, MMIHS5 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 102545; MGI: 104589; HomoloGene: 123845; GeneCards: ACTG2; OMA:ACTG2 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Actin, gamma-enteric smooth muscle is a protein that in humans is encoded by the ACTG2 gene. [5] [6] [7]
Actins are highly conserved proteins that are involved in various types of cell motility, and maintenance of the cytoskeleton. In vertebrates, three main groups of actin isoforms, alpha, beta and gamma have been identified. The alpha actins are found in muscle tissues and are a major constituent of the contractile apparatus. The beta and gamma actins co-exist in most cell types as components of the cytoskeleton, and as mediators of internal cell motility. Actin, gamma 2, encoded by this gene, is a smooth muscle actin found in enteric tissues. [7]
Cofilin 1 , also known as CFL1, is a human gene, part of the ADF/cofilin family.
Actin, alpha skeletal muscle is a protein that in humans is encoded by the ACTA1 gene.
Tropomyosin alpha-1 chain is a protein that in humans is encoded by the TPM1 gene. This gene is a member of the tropomyosin (Tm) family of highly conserved, widely distributed actin-binding proteins involved in the contractile system of striated and smooth muscles and the cytoskeleton of non-muscle cells.
T-cell surface glycoprotein CD3 gamma chain is a protein that in humans is encoded by the CD3G gene.
Serine/threonine-protein phosphatase PP1-beta catalytic subunit is an enzyme that in humans is encoded by the PPP1CB gene.
Actin, cytoplasmic 2, or gamma-actin is a protein that in humans is encoded by the ACTG1 gene. Gamma-actin is widely expressed in cellular cytoskeletons of many tissues; in adult striated muscle cells, gamma-actin is localized to Z-discs and costamere structures, which are responsible for force transduction and transmission in muscle cells. Mutations in ACTG1 have been associated with nonsyndromic hearing loss and Baraitser-Winter syndrome, as well as susceptibility of adolescent patients to vincristine toxicity.
Alpha-actinin-1 is a protein that in humans is encoded by the ACTN1 gene.
Spectrin alpha chain, erythrocyte is a protein that in humans is encoded by the SPTA1 gene.
ACTC1 encodes cardiac muscle alpha actin. This isoform differs from the alpha actin that is expressed in skeletal muscle, ACTA1. Alpha cardiac actin is the major protein of the thin filament in cardiac sarcomeres, which are responsible for muscle contraction and generation of force to support the pump function of the heart.
Tropomyosin alpha-3 chain is a protein that in humans is encoded by the TPM3 gene.
ACTA2 is an actin protein with several aliases including alpha-actin, alpha-actin-2,aortic smooth muscle or alpha smooth muscle actin. Actins are a family of globular multi-functional proteins that form microfilaments. ACTA2 is one of 6 different actin isoforms and is involved in the contractile apparatus of smooth muscle. ACTA2 is extremely highly conserved and found in nearly all mammals.
Serine/threonine-protein kinase D3 (PKD3) or PKC-nu is an enzyme that in humans is encoded by the PRKD3 gene.
Transgelin is a protein that in humans is encoded by the TAGLN gene.
Eukaryotic translation initiation factor 2 subunit 3 (eIF2γ) is a protein that in humans is encoded by the EIF2S3 gene.
Zinc finger protein 40 is a protein that in humans is encoded by the HIVEP1 gene.
Myosin-14 is a protein that in humans is encoded by the MYH14 gene.
Interferon alpha-7 is a protein that in humans is encoded by the IFNA7 gene.
Troponin C, skeletal muscle is a protein that in humans is encoded by the TNNC2 gene.
GBA2 is the gene that encodes the enzyme non-lysosomal glucosylceramidase in humans. It has glucosylceramidase activity.
Cofilin 2 (muscle) also known as CFL2 is a protein which in humans is encoded by the CFL2 gene.
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: CS1 maint: DOI inactive as of September 2024 (link)