COMMD6 COMM domain containing 6
Gene ID: 170622, updated on 19-Sep-2024Gene type: protein coding
Also known as: Acrg
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- Go to complete Gene record for COMMD6
- Go to Variation Viewer for COMMD6 variants
Summary
COMMD6 belongs to a family of NF-kappa-B (see RELA; MIM 164014)-inhibiting proteins characterized by the presence of a COMM domain (see COMMD1; MIM 607238) (de Bie et al., 2006 [PubMed 16573520]).[supplied by OMIM, Mar 2009]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Genome-wide association study in a Chinese population with diabetic retinopathy. GeneReviews: Not available |
Genomic context
- Location:
- 13q22.2
- Sequence:
- Chromosome: 13; NC_000013.11 (75525214..75549439, complement)
- Total number of exons:
- 6
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for COMMD6 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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