NUGGC nuclear GTPase, germinal center associated
Gene ID: 389643, updated on 17-Sep-2024Gene type: protein coding
Also known as: SLIPGC; C8orf80; SLIP-GC; HMFN0672
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- Go to complete Gene record for NUGGC
- Go to Variation Viewer for NUGGC variants
Summary
Enables GTPase activity. Involved in cellular response to lipopolysaccharide; negative regulation of apoptotic process; and regulation of nuclear cell cycle DNA replication. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Association of genome-wide variation with highly sensitive cardiac troponin-T levels in European Americans and Blacks: a meta-analysis from atherosclerosis risk in communities and cardiovascular health studies. GeneReviews: Not available | |
| Genome-wide association study of increasing suicidal ideation during antidepressant treatment in the GENDEP project. GeneReviews: Not available |
Genomic context
- Location:
- 8p21.1
- Sequence:
- Chromosome: 8; NC_000008.11 (28021964..28083936, complement)
- Total number of exons:
- 20
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for NUGGC 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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