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Results for Proteins associated with the Gene: FOXG1
FOXG1
2290


Known Diseases associated with this Protein:
  RETT SYNDROME CONGENITAL VARIANT (RTTCV)
  RETT SYNDROME, CONGENITAL VARIANT
7
1
5
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:

FH - smart00339
Fork_head - pfam00250
FH - cd00059


Swiss-Prot Protein: P55316
Identical to: NP_005240
   Default View:




Default View:

FH - smart00339
Fork_head - pfam00250
FH - cd00059


RefSeq Protein: NP_005240
   Default View:





Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
P55316FHcd000591812581e-60
P55316Fork_headpfam002501812761.1e-70
P55316FHsmart003391812693.3e-62
NP_005240FHcd000591812581e-60
NP_005240Fork_headpfam002501812761.1e-70
NP_005240FHsmart003391812693.3e-62



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