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ACTG1 actin gamma 1 [Homo sapiens (human)] - Gene - NCBI Actin gamma 1, encoded by this gene, is a cytoplasmic actin found in all cell types Mutations in this gene are associated with DFNA20 26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss and also with Baraitser-Winter syndrome
ACTG1 Gene - GeneCards | ACTG Protein | ACTG Antibody Actin gamma 1, encoded by this gene, is a cytoplasmic actin found in all cell types Mutations in this gene are associated with DFNA20 26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss and also with Baraitser-Winter syndrome
Entry - *102560 - ACTIN, GAMMA-1; ACTG1 - OMIM - (OMIM. ORG) HGNC Approved Gene Symbol: ACTG1 Cytogenetic location: 17q25 3 Genomic coordinates (GRCh38) : 17:81,509,971-81,512,799 (from NCBI) Actins are a family of highly conserved cytoskeletal proteins that play fundamental roles in nearly all aspects of eukaryotic cell biology
Actin, cytoplasmic 2 - Wikipedia 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
ACTG1 gene: MedlinePlus Genetics The ACTG1 gene provides instructions for making a protein called gamma (γ)-actin, which is part of the actin protein family Proteins in this family are organized into a network of fibers called the actin cytoskeleton, which makes up the structural framework inside cells
What Is the ACTG1 Gene and What Are Its Functions? What is ACTG1 and Gamma-Actin? The ACTG1 gene, or Actin Gamma 1, is located on human chromosome 17 It produces gamma-actin Gamma-actin belongs to the broader actin protein family, a highly conserved family found across many species
ACTG1 gene information - The Human Protein Atlas Actin gamma 1, encoded by this gene, is a cytoplasmic actin found in all cell types Mutations in this gene are associated with DFNA20 26, a subtype of autosomal dominant non-syndromic sensorineural progressive hearing loss and also with Baraitser-Winter syndrome
Orphanet: ACTG1-actin gamma 1 Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources
Human Gene ACTG1 (ENST00000573283. 7) from GENCODE V47 - BLAT Each actin can bind to 4 others SUBCELLULAR LOCATION: Cytoplasm, cytoskeleton PTM: The methylhistidine determined by Bienvenut et al is assumed to be the tele-methylhistidine isomer by similarity to the mouse ortholog
Gene: ACTG1 (ENSG00000184009) - Summary - Homo_sapiens - Ensembl View alleles of this gene on alternative sequences This gene has 15 transcripts (splice variants), 1 gene allele, 186 orthologues, 26 paralogues and is associated with 10 phenotypes Show transcript table