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Summary

Isoform:
Position:
22
Ref:
P
Mutation:
T
PTM impact:
network-rewiring
PTM affected:
4
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

no data

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

[0.0199681]

PTM Site: 21S

Affected site:

Position: 21
Residue: S
Type: phosphorylation

Best loss of PTM site:

MAPK10 (probability p=0.99)
Site: 21S (phosphorylation)
Position in motif: 1
There are 10 other predicted losses:
  • MAPK3 (p=0.953)
  • MAPK1 (p=0.948)
  • MAPK14 (p=0.944)
  • MTOR (p=0.93)
  • GSK3B (p=0.921)
  • CDK1 (p=0.921)
  • CDK5 (p=0.895)
  • MAPK7 (p=0.885)
  • CDK2 (p=0.882)
  • MAPK9 (p=0.864)

Other known mutations affecting this site

Mutation In sequence Distance Impact
22T PEARDARS[P/T]PSGPSGS 1
network-rewiring
20G PEARDA[R/G]RSPSGPSGS 1
proximal
26N PEARDARSPSGP[S/N]SGS 5
distal
23L PEARDARSP[S/L]SGPSGS 2
proximal

PTM Site: 23S

Affected site:

Position: 23
Residue: S
Type: phosphorylation

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
22T ARDARS[P/T]PSGPSGSLE 1
proximal
20G ARDA[R/G]RSPSGPSGSLE 3
network-rewiring
26N ARDARSPSGP[S/N]SGSLE 3
distal
23L ARDARSP[S/L]SGPSGSLE 0
direct

PTM Site: 26S

Affected site:

Position: 26
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
30K ARSPSGPSGSL[E/K]ENGT 4
distal
22T ARS[P/T]PSGPSGSLENGT 4
distal
20G A[R/G]RSPSGPSGSLENGT 6
distal
26N ARSPSGP[S/N]SGSLENGT 0
direct
23L ARSP[S/L]SGPSGSLENGT 3
distal

PTM Site: 28S

Affected site:

Position: 28
Residue: S
Type: phosphorylation

Impact:

distal

Other known mutations affecting this site

Mutation In sequence Distance Impact
30K SPSGPSGSL[E/K]ENGTKA 2
network-rewiring
22T S[P/T]PSGPSGSLENGTKA 6
distal
26N SPSGP[S/N]SGSLENGTKA 2
proximal
23L SP[S/L]SGPSGSLENGTKA 5
distal

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