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Results for the Protein: Q14999
160370003

CUL7_HUMAN RecName: Full=Cullin-7; Short=CUL-7

Known Diseases associated with this Protein:
  3@M SYNDROME
  3M SYNDROME 1 (3M1)
5
4
2
4
3
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

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Default View:

Cul7 - pfam11515
APC10-HERC2 - cd08664
APC10-ZZEF1 - cd08667
APC10-CUL7 - cd08665
APC10-like1 - cd08365
APC10-like - cd08159
APC10-HECTD3 - cd08666
APC10 - cd08366
Cullin - pfam00888


Swiss-Prot Protein: Q14999
Identical to: NP_055595
   Default View:









Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
APC10-like1cd083652.8e-99838967
APC10-CUL7cd086659e-106838968
APC10-ZZEF1cd086675e-33838968
APC10-likecd081592.5e-88839967
APC10-HECTD3cd086663.2e-32839967
APC10cd083662.6e-07844968
Cullinpfam008881.2e-11910431545
Cul7pfam115152.2e-50360435

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs34574340 Polymorphismp.ARG852GLNN/A
dbSNPrs9381231 Polymorphismp.GLN813ARGN/A
Swiss-ProtVAR_026123Diseasep.GLN1246GLY3M syndrome 1 (3M1)
dbSNPrs36071170 Polymorphismp.GLN1246HISN/A
Swiss-ProtVAR_026124Diseasep.HIS1464PRO3M syndrome 1 (3M1)
Swiss-ProtVAR_026122Diseasep.LEU1014ARG3M syndrome 1 (3M1)
dbSNPrs7774330 Polymorphismp.SER616GLYN/A
OMIM609577.0001 Diseasep.ARG1361TER3@M SYNDROME
OMIM609577.0002 Diseasep.HIS1380PRO3@M SYNDROME



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