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Results for Proteins associated with the Gene: ALG9
ALG9
79796


Known Diseases associated with this Protein:
  CONGENITAL DISORDER OF GLYCOSYLATION 1L (CDG1L)
  CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IL
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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:

Glyco_transf_22 - pfam03901


Swiss-Prot Protein: Q9H6U8
Identical to: NP_001071158
   Default View:


Default View:

Glyco_transf_22 - pfam03901



Default View:

Glyco_transf_22 - pfam03901



Default View:

Glyco_transf_22 - pfam03901



Default View:

Glyco_transf_22 - pfam03901


RefSeq Protein: NP_079016
   Default View:



Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
Q9H6U8Glyco_transf_22pfam03901604825e-202
NP_001071159Glyco_transf_22pfam0390113184.6e-78
NP_001071160Glyco_transf_22pfam0390113111.1e-83
NP_001071158Glyco_transf_22pfam03901604825e-202
NP_079016Glyco_transf_22pfam03901604892.4e-196



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