DDX59
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 1[12]
- Cytogenetic location
- 1q32.1[15]
- Encodes
- DEAD-box helicase 59, Probable ATP-dependent RNA helicase DDX59[9][10]
- Expressed in
- buccal mucosa cell, pancreatic ductal cell, tendon of biceps brachii, oocyte, secondary oocyte, cardia, endothelial cell, mucosa of paranasal sinus, renal medulla, nipple[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- orofaciodigital syndrome V[13]
- HomoloGene ID
- 12222[3]
- Strand orientation
- reverse strand[14]
🏷️ Also known as
en DDX59
en DEAD-box helicase 59
en OFD5
en ZNHIT5
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000118197
- Ensembl transcript ID
- ENST00000453944, ENST00000331314, ENST00000413408, ENST00000429498, ENST00000433235, ENST00000436897, ENST00000447706, ENST00000452560
- Entrez Gene ID
- 83479
- Exact match
- identifiers.org
- Freebase ID
- /m/0408mz6
- HGNC ID
- 25360
- HGNC gene symbol
- DDX59
- OMIM ID
- 615464
- RefSeq RNA ID
- XR_921967, NM_001031725, NM_031306, XR_921966, NM_001320181, NM_001320182, XM_017002432, XR_001737463, NM_001349799, NM_001349800, NM_001349801, NM_001349802, NM_001349803, NM_001349804
- UMLS CUI
- C1539234
🔗 Connections
Expressed in 4
Chromosome 1
Found in taxon 1
Instance of 1
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