NAV3 neuron navigator 3
Gene ID: 89795, updated on 7-Aug-2024Gene type: protein coding
Also known as: POMFIL1; unc53H3; STEERIN3
- See all available tests in GTR for this gene
- Go to complete Gene record for NAV3
- Go to Variation Viewer for NAV3 variants
Summary
This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. Multiple alternatively spliced transcript variants for this gene have been described but only one has had its full-length nature determined. [provided by RefSeq, Jul 2008]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
A genome-wide association study of self-rated health. GeneReviews: Not available | |
A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. GeneReviews: Not available | |
Genome-wide and candidate gene association study of cigarette smoking behaviors. GeneReviews: Not available | |
Genome-wide association study of ancestry-specific TB risk in the South African Coloured population. GeneReviews: Not available |
Genomic context
- Location:
- 12q21.2
- Sequence:
- Chromosome: 12; NC_000012.12 (77571862..78213010)
- Total number of exons:
- 42
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for NAV3 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
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.