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Results for Proteins associated with the Gene: UGT1A1
UGT1A1
54658


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)
55
1
13
1
42
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:



Swiss-Prot Protein: P22309
Identical to: NP_000454
   Default View:

Default View:

COG1819 - COG1819
UDPGT - pfam00201
GT1_Gtf_like - cd03784


RefSeq Protein: NP_000454
   Default View:





Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
P22309NO_DOMAIN_FOUND00
NP_000454COG1819COG1819274738.3e-07
NP_000454GT1_Gtf_likecd03784284614.3e-11
NP_000454UDPGTpfam0020128525



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