ACTB
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 7[22]
- Cytogenetic location
- 7p22.1[26]
- Encodes
- Actin beta, Actin, cytoplasmic 1[19][20]
- Expressed in
- saphenous vein, urethra, postcentral gyrus, synovial joint, orbitofrontal cortex, mucosa of ileum, Brodmann area 46, nipple, vena cava, olfactory bulb[27][28][29][30][31][32][33][34][35][36]
- Found in taxon
- Homo sapiens[21]
- Genetic association
- developmental malformations-deafness-dystonia syndrome, Baraitser-Winter syndrome[23][24]
- HomoloGene ID
- 110648[3]
- Ortholog
- Actb, Actb, Act87E, Act57B, Actg1, act-2, act-4, Actg1, actb2, Act42A, Act5C[10][11][12][13][14][15][16][17][18]
- Strand orientation
- reverse strand[25]
🏷️ Also known as
en ACTB
en actin beta
en actin, beta
en Beta-actin
en BRWS1
en PS1TP5BP1
ja Β-アクチン
uk Бета-актин
zh Β-肌动蛋白
🔖 Identifiers · 12
- Image (Wikimedia Commons)
- Protein ACTB PDB 1atn.png ↗
- Ensembl gene ID
- ENSG00000075624
- Ensembl transcript ID
- ENST00000493945, ENST00000414620, ENST00000417101, ENST00000425660, ENST00000432588, ENST00000443528, ENST00000462494, ENST00000464611, ENST00000473257, ENST00000477812, ENST00000480301, ENST00000484841, ENST00000642480, ENST00000645025, ENST00000645576, ENST00000646584, ENST00000646664, ENST00000647275, ENST00000676397, ENST00000676319, ENST00000674681, ENST00000676189, ENST00000675515
- Entrez Gene ID
- 60
- Exact match
- identifiers.org
- Freebase ID
- /m/03ct2hr
- HGNC ID
- 132
- HGNC gene symbol
- ACTB
- Microsoft Academic ID (discontinued)
- 2780674356, 2910681310
- OMIM ID
- 102630
- RefSeq RNA ID
- NM_001101
- UMLS CUI
- C1384510
🔗 Connections
Expressed in 8
Chromosome 1
Found in taxon 1
Instance of 1
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