CUX2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 12[12]
- Cytogenetic location
- 12q24.11-q24.12[16]
- Encodes
- Cut like homeobox 2[10]
- Expressed in
- middle temporal gyrus, buccal mucosa cell, Brodmann area 23, endothelial cell, lateral nuclear group of thalamus, Epithelium of choroid plexus, primary visual cortex, ganglionic eminence, Brodmann area 46, postcentral gyrus[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[11]
- Genetic association
- coronary artery disease, type-1 diabetes[13][14]
- HomoloGene ID
- 22426[3]
- Strand orientation
- forward strand[15]
🏷️ Also known as
en CDP2
en CUTL2
en cut like homeobox 2
en CUX2
en DEE67
en EIEE67
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000111249
- Ensembl transcript ID
- ENST00000551604, ENST00000261726, ENST00000397643
- Entrez Gene ID
- 23316
- Exact match
- identifiers.org
- Google Knowledge Graph ID
- /g/11gbldnfz9
- HGNC ID
- 19347
- HGNC gene symbol
- CUX2
- OMIM ID
- 610648
- RefSeq RNA ID
- NM_015267, XM_011538063, XM_011538069, XM_011538070, XM_017019080, XM_017019081, NM_001370598
- UMLS CUI
- C1426179
Press Enter · cited answer in seconds