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Results for Proteins associated with the Gene: ERCC2
ERCC2
2068


Known Diseases associated with this Protein:
  CEREBROOCULOFACIOSKELETAL SYNDROME
  CEREBROOCULOFACIOSKELETAL SYNDROME 2
  TRICHOTHIODYSTROPHY
  TRICHOTHIODYSTROPHY PHOTOSENSITIVE (TTDP)
  TRICHOTHIODYSTROPHY, INCLUDED
  XERODERMA PIGMENTOSUM COMPLEMENTATION GROUP D (XP-D)
  XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D
  XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP D, INCLUDED
42
6
12
2
34
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:

- smart00489
DEXDc2 - smart00488
DEAD_2 - pfam06733
DUF1227 - pfam06777
- smart00492
HELICc2 - smart00491


Swiss-Prot Protein: P18074
Identical to: NP_000391
   Default View:




Default View:

DinG - COG1199
- smart00489
DEXDc2 - smart00488
DEAD_2 - pfam06733
DUF1227 - pfam06777
- smart00492
HELICc2 - smart00491


RefSeq Protein: NP_000391
   Default View:





Default View:

DEXDc2 - smart00488
- smart00489
DEAD_2 - pfam06733
DUF1227 - pfam06777




Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
NP_001124339smart0048912563.8e-118
NP_001124339DEAD_2pfam06733482324.3e-68
NP_001124339DUF1227pfam067772443894.7e-95



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