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Results for Proteins associated with the Gene: MYCN
MYCN
4613


Known Diseases associated with this Protein:
  FEINGOLD SYNDROME
  FEINGOLD SYNDROME 1 (FGLDS1)
9
0
6
0
3
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:

HLH - smart00353


Swiss-Prot Protein: P04198
Identical to: NP_005369
   Default View:


Default View:

Myc_N - pfam01056
HLH - cd00083
HLH - pfam00010
HLH - smart00353


RefSeq Protein: NP_005369
   Default View:





Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
NP_005369Myc_Npfam0105693723.1e-219
NP_005369HLHpfam000103824349.9e-19
NP_005369HLHsmart003533874392.5e-17



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