NKX2-5
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene[2]
- Chromosome
- human chromosome 5[13]
- Cytogenetic location
- 5q35.1[17]
- Encodes
- NK2 homeobox 5, Homeobox protein Nkx-2.5[10][11]
- Expressed in
- apex of heart, right auricle of heart, left ventricle, right ventricle, myocardium of left ventricle, cardiac muscle tissue of right atrium, spleen, gonad, vena cava, body of tongue[18][19][20][21][22][23][24][25][26][27]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- atrial heart septal defect 7, tetralogy of Fallot[14][15]
- HomoloGene ID
- 3230[3]
- Strand orientation
- reverse strand[16]
🏷️ Also known as
en CHNG5
en CSX
en CSX1
en HLHS2
en NK2 homeobox 5
en NKX2-5
en NKX2.5
en NKX2E
en NKX4-1
en VSD3
ja Nkx2-5
🔖 Identifiers · 12
- OpenAlex ID
- C180504324
- Ensembl gene ID
- ENSG00000183072
- Ensembl transcript ID
- ENST00000521848, ENST00000329198, ENST00000424406, ENST00000517440
- Entrez Gene ID
- 1482
- Exact match
- identifiers.org
- Freebase ID
- /m/03gwrfq
- HGNC ID
- 2488
- HGNC gene symbol
- NKX2-5
- Microsoft Academic ID (discontinued)
- 180504324
- OMIM ID
- 600584
- RefSeq RNA ID
- NM_004387, NM_001166175, NM_001166176, XM_017009071
- UMLS CUI
- C1413784
🔗 Connections
Expressed in 5
← Genetic association 3
Chromosome 1
Found in taxon 1
Genetic association 1
Instance of 1
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Summary
NKX2-5 is a gene[1].