ACTA2
Sign in to saveAlso known as AAT6, ACTSA, MYMY5, actin, alpha 2, smooth muscle, aorta, actin alpha 2, smooth muscle
Gen der Spezies Homo sapiens
Gene data
ACTA2- Name
- actin alpha 2, smooth muscle
- Type
- protein-coding
- Position
- 88,934,815–88,991,339 (−)
- Aliases
- ACTSA, SMDYS
- Ensembl
- ENSG00000107796
- RefSeq RNA
- NM_001141945.3, NM_001320855.2, NM_001406462.1, NM_001406463.1, NM_001406464.1
- RefSeq protein
- NP_001135417.1, NP_001307784.1, NP_001393391.1, NP_001393392.1, NP_001393393.1
This gene encodes one of six different actin proteins. Actins are highly conserved proteins that are involved in cell motility, structure, integrity, and intercellular signaling. The encoded protein is a smooth muscle actin that is involved in vascular contractility and blood pressure homeostasis. Mutations in this gene cause a variety of vascular diseases, such as thoracic aortic disease, coronary artery disease, stroke, and Moyamoya disease, as well as multisystemic smooth muscle dysfunction syndrome. [provided by RefSeq, Sep 2017].
Gene Ontology
Biological process
Molecular function
Pathways
via MyGene.info
Gene · Ensembl
actin alpha 2, smooth muscle
- Symbol
- ACTA2
- Biotype
- Protein coding
- Organism
- Homo sapiens
- Location
- 10:88,934,815-88,991,339
- Strand
- Reverse (−)
- Assembly
- GRCh38
via Ensembl · EMBL-EBI
Wikidata facts
- Instance of
- gene
- Image
- Protein ACTA2 PDB 1atn.png
Show 7 more facts
- HomoloGene ID
- 133938
- found in taxon
- Homo sapiens
- exact match
- identifiers.org/ncbigene/59
- genomic end
- 90751147
- genomic start
- 90694831
- chromosome
- human chromosome 10
- cytogenetic location
- 10q23.31
via Wikidata · CC0