FRA16E fragile site, distamycin A type, rare, fra(16)(p12.1)
Gene ID: 2464, updated on 17-Aug-2024Gene type: other
Also known as: C16DELp12.1
Associated conditions
| Description | Tests |
|---|---|
| Chromosome 16p12.1 deletion syndrome, 520kb | See labs |
Genomic context
- Location:
- 16p12.1
Variation
| Resource | Links for this gene |
|---|---|
| SNP | Variation Viewer for FRA16E variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- MedGenRelated information in MedGen
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
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.