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Known Diseases associated with this Protein: |  BILIRUBIN, SERUM LEVEL OF, QUANTITATIVE T
| CRIGLER-NAJJAR SYNDROME 1 (CN1)
| CRIGLER-NAJJAR SYNDROME 2 (CN2)
| CRIGLER-NAJJAR SYNDROME, TYPE I
| CRIGLER-NAJJAR SYNDROME, TYPE II
| CRIGLER-NAJJAR SYNDROME, TYPE II, INCLUDED
| GILBERT SYNDROME
| GILBERT SYNDROME (GILBS)
| GILBERT SYNDROME, INCLUDED
| HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATAL
| HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATAL, INCLUDED;;
| TRANSIENT FAMILIAL NEONATAL HYPERBILIRUBINEMIA (HBLRTFN)
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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. |
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Domains found on the Proteins
Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.
| DMDM_info@umbc.edu | 1000 Hilltop Circle, Baltimore, MD
21250 | Department of Biological Sciences | Phone: 410-455-2258 |
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UGT1A1
54658
55
1
13
1
42
