ACTG1
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 17[22]
- Cytogenetic location
- 17q25.3[27]
- Encodes
- Actin gamma 1, Actin, cytoplasmic 2[19][20]
- Expressed in
- mucosa of ileum, ventricular zone, amniotic fluid, embryo, ganglionic eminence, parietal pleura, epithelium of nasopharynx, visceral pleura, spinal ganglia, pericardium[28][29][30][31][32][33][34][35][36][37]
- Found in taxon
- Homo sapiens[21]
- Genetic association
- autosomal dominant nonsyndromic deafness 20, nonsyndromic deafness, Baraitser-Winter syndrome[23][24][25]
- HomoloGene ID
- 74402[3]
- Ortholog
- Actg1, Actg1, ACT1, Act5C, actb1, actb2, act-4, act-2, act-3, act-1, Actb, Actb, Act42A[8][9][10][11][12][13][14][15][16][17][18]
- Strand orientation
- reverse strand[26]
🏷️ Also known as
en ACT
en ACTG
en ACTG1
en actin gamma 1
en BRWS2
en DFNA20
en DFNA26
en HEL-176
uk Гамма-актин-1
zh Γ-肌动蛋白
🔖 Identifiers · 12
- Image (Wikimedia Commons)
- Protein ACTG1 PDB 1atn.png ↗
- Ensembl gene ID
- ENSG00000184009
- Ensembl transcript ID
- ENST00000615544, ENST00000570382, ENST00000571691, ENST00000571721, ENST00000572105, ENST00000573283, ENST00000574671, ENST00000575087, ENST00000575659, ENST00000575842, ENST00000575994, ENST00000576209, ENST00000576214, ENST00000576544, ENST00000576917, ENST00000644774, ENST00000679778, ENST00000679535, ENST00000680727, ENST00000681052, ENST00000681092, ENST00000681842, ENST00000680227, ENST00000679480, ENST00000679410
- Entrez Gene ID
- 71
- Exact match
- identifiers.org
- Freebase ID
- /m/03d0ls3
- HGNC ID
- 144
- HGNC gene symbol
- ACTG1
- Microsoft Academic ID (discontinued)
- 2778000619
- OMIM ID
- 102560
- RefSeq RNA ID
- NR_037688, NM_001199954, NM_001614
- UMLS CUI
- C1412149
🔗 Connections
Expressed in 6
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
← Genetic association 1
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