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Results for Proteins associated with the Gene: SOX10
SOX10
6663


Known Diseases associated with this Protein:
  PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATING LEUKODYSTROPHY, WAARDENBURG SYNDROME AND HIRSCHSPRUNG DISEAS
  PERIPHERAL DEMYELINATING NEUROPATHY, CENTRAL DYSMYELINATION, WAARDENBURG
  SYNDROME, AND HIRSCHSPRUNG DISEASE
  WAARDENBURG SYNDROME 2E (WS2E)
  WAARDENBURG SYNDROME 4C (WS4C)
  WAARDENBURG SYNDROME, TYPE 2E, WITH NEUROLOGIC INVOLVEMENT
  WAARDENBURG SYNDROME, TYPE 2E, WITH NEUROLOGIC INVOLVEMENT, INCLUDED
  WAARDENBURG SYNDROME, TYPE 2E, WITHOUT NEUROLOGIC INVOLVEMENT
  WAARDENBURG SYNDROME, TYPE 4C
23
0
10
0
13
Tips:
 The Domains on the Default View are decided by HMMER's search E-Value of the Protein against the Domain model.
 Clicking a check box on the left will display or hide the corresponding domain(s).
 To view the Protein page, either click on the protein links in the box to the left or the blue bar above the Protein's graphic.


Default View:

Sox_N - pfam12444
HMG - smart00398


Swiss-Prot Protein: P56693
Identical to: NP_008872
   Default View:


Default View:

Sox_N - pfam12444
SOX-TCF_HMG-box - cd01388
MATA_HMG-box - cd01389
HMG - smart00398
HMGB-UBF_HMG-box - cd01390
HMG-box - cd00084
HMG_box - pfam00505


RefSeq Protein: NP_008872
   Default View:








Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
NP_008872MATA_HMG-boxcd013891031791e-18
NP_008872HMG-boxcd000841041695.5e-21
NP_008872HMGB-UBF_HMG-boxcd013901041691.3e-13
NP_008872HMG_boxpfam005051041728.5e-32
NP_008872Sox_Npfam1244411945.7e-37
NP_008872HMGsmart003981031721.9e-27



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