CUX2 cut like homeobox 2
Gene ID: 23316, updated on 19-Jun-2024Gene type: protein coding
Also known as: CDP2; CUTL2; DEE67; EIEE67
- See all available tests in GTR for this gene
- Go to complete Gene record for CUX2
- Go to Variation Viewer for CUX2 variants
Summary
This gene encodes a protein which contains three CUT domains and a homeodomain; both domains are DNA-binding motifs. A similar gene, whose gene product possesses different DNA-binding activities, is located on chromosome on chromosome 7. Two pseudogenes of this gene have been identified on chromosomes 10 and 4. [provided by RefSeq, Jan 2013]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| 1000 Genomes-based imputation identifies novel and refined associations for the Wellcome Trust Case Control Consortium phase 1 Data. GeneReviews: Not available | |
| A genome-wide association study of a coronary artery disease risk variant. GeneReviews: Not available | |
| Developmental and epileptic encephalopathy, 67 | See labs |
Genomic context
- Location:
- 12q24.11-q24.12
- Sequence:
- Chromosome: 12; NC_000012.12 (111034165..111350554)
- Total number of exons:
- 26
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for CUX2 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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