# Tubulin beta 2B class IIb

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21102151](https://www.wikidata.org/wiki/Q21102151)  
**Source**: https://4ort.xyz/entity/tubulin-beta-2b-class-iib-q21102151


## References

1. UniProt
2. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL159)
3. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1201752)
4. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL1096380)
5. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL378544)
6. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL94657)
7. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL501867)
8. [Open Targets Platform](https://platform.opentargets.org/drug/CHEMBL39541)
9. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9BVA1)
10. Q20641742
11. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9BVA1)
12. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9BVA1&geneProductId=UniProtKB:Q9BVA1)
13. [Comparison of an expanded ataxia interactome with patient medical records reveals a relationship between macular degeneration and ataxia](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9BVA1)
14. [Uner Tan syndrome caused by a homozygous TUBB2B mutation affecting microtubule stability](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9BVA1)
15. [An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9BVA1)
16. [De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathy](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9BVA1)
17. [Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9BVA1)
18. [PEX14 is required for microtubule-based peroxisome motility in human cells](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9BVA1&geneProductId=UniProtKB:Q9BVA1)
19. [Proteomic characterization of the human sperm nucleus](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9BVA1&geneProductId=UniProtKB:Q9BVA1)
20. [Proteomic characterization of the human sperm nucleus](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9BVA1)
21. [PEX14 is required for microtubule-based peroxisome motility in human cells](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9BVA1)
22. [Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9BVA1&geneProductId=UniProtKB:Q9BVA1)
23. [De novo TUBB2B mutation causes fetal akinesia deformation sequence with microlissencephaly: An unusual presentation of tubulinopathy](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9BVA1&geneProductId=UniProtKB:Q9BVA1)
24. [Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9BVA1)
25. Ensembl Release 99