TUBB6 tubulin beta 6 class V
Gene ID: 84617, updated on 14-Nov-2024Gene type: protein coding
Also known as: FPVEPD; TUBB-5; HsT1601
- See all available tests in GTR for this gene
- Go to complete Gene record for TUBB6
- Go to Variation Viewer for TUBB6 variants
Summary
Predicted to enable GTP binding activity. Predicted to be a structural constituent of cytoskeleton. Predicted to be involved in microtubule cytoskeleton organization and mitotic cell cycle. Located in intercellular bridge; microtubule; and mitotic spindle. [provided by Alliance of Genome Resources, Nov 2024]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Facial palsy, congenital, with ptosis and velopharyngeal dysfunction | not available |
Genomic context
- Location:
- 18p11.21
- Sequence:
- Chromosome: 18; NC_000018.10 (12307669..12329826)
- Total number of exons:
- 7
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for TUBB6 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- 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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