RBFA ribosome binding factor A
Gene ID: 79863, updated on 2-Nov-2024Gene type: protein coding
Also known as: HsT169; C18orf22
- See all available tests in GTR for this gene
- Go to complete Gene record for RBFA
- Go to Variation Viewer for RBFA variants
Summary
Predicted to be involved in rRNA processing. Located in mitochondrion. [provided by Alliance of Genome Resources, Nov 2024]
Genomic context
- Location:
- 18q23
- Sequence:
- Chromosome: 18; NC_000018.10 (80034434..80050651)
- Total number of exons:
- 7
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for RBFA 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.