DCUN1D2 defective in cullin neddylation 1 domain containing 2
Gene ID: 55208, updated on 3-Apr-2024Gene type: protein coding
Also known as: DCNL2; C13orf17
- See all available tests in GTR for this gene
- Go to complete Gene record for DCUN1D2
- Go to Variation Viewer for DCUN1D2 variants
Summary
Enables cullin family protein binding activity. Involved in positive regulation of protein neddylation. Located in cytoplasm and nucleus. [provided by Alliance of Genome Resources, Apr 2022]
Genomic context
- Location:
- 13q34
- Sequence:
- Chromosome: 13; NC_000013.11 (113455819..113491563, complement)
- Total number of exons:
- 10
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for DCUN1D2 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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