After several years of serving the research community, our ActiveDriverDB database will be retired on May 1st 2026. Please make sure to download any data you need and update your links or workflows before that date.

We want to sincerely thank all our users for their support, feedback, and collaboration over the years — your contributions have been invaluable to this project. A special thank you to Dr. Michal Krassowski for leading the development of our open-source software and database.

For any questions or assistance, please contact Jüri Reimand (juri.reimand@utoronto.ca).

You are viewing an updated version (2021) of the ActiveDriverDB. To view the previous version please visit activedriverdb.org/v2020

Summary

Isoform:
Position:
445
Ref:
Q
Mutation:
R
PTM impact:
network-rewiring
PTM affected:
2
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

Hereditary cancer-predisposing syndrome

Minor Allele Frequency: (ESP6500)

[0.0077]

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 442K

Affected site:

Position: 442
Residue: K
Type: ubiquitination

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
445R QYFQTAEKNV[Q/R]QLSLL 3
distal
440S QYFQT[A/S]AEKNVQLSLL 2
proximal
440T QYFQT[A/T]AEKNVQLSLL 2
proximal
439I QYFQ[T/I]TAEKNVQLSLL 3
distal
438E QYF[Q/E]QTAEKNVQLSLL 4
distal
436H Q[Y/H]YFQTAEKNVQLSLL 6
distal
436N Q[Y/N]YFQTAEKNVQLSLL 6
distal

PTM Site: 447S

Affected site:

Position: 447
Residue: S
Type: phosphorylation

Best gain of PTM site:

AURKA (probability p=0.994)
Site: 447S (phosphorylation)
Position in motif: -2
There are 4 other predicted gains:
  • PRKACA (p=0.957)
  • AURKB (p=0.934)
  • PRKG1 (p=0.891)
  • ROCK1 (p=0.88)

Other known mutations affecting this site

Mutation In sequence Distance Impact
453A AEKNVQLSLLTER[G/A]GM 6
distal
445R AEKNV[Q/R]QLSLLTERGM 2
network-rewiring
453W AEKNVQLSLLTER[G/W]GM 6
distal
451Q AEKNVQLSLLT[E/Q]ERGM 4
distal

External references

dbSNP:

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