Structural highlights
Disease
GCP6_HUMAN Autosomal recessive chorioretinopathy-microcephaly syndrome. The disease is caused by mutations affecting the gene represented in this entry.
Function
GCP6_HUMAN Gamma-tubulin complex is necessary for microtubule nucleation at the centrosome.[1]
See Also
References
- ↑ Murphy SM, Preble AM, Patel UK, O'Connell KL, Dias DP, Moritz M, Agard D, Stults JT, Stearns T. GCP5 and GCP6: two new members of the human gamma-tubulin complex. Mol Biol Cell. 2001 Nov;12(11):3340-52. PMID:11694571