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Results for Proteins associated with the Gene: BCS1L
BCS1L
617


Known Diseases associated with this Protein:
  BJOERNSTAD SYNDROME (BJS)
  BJORNSTAD SYNDROME
  BJORNSTAD SYNDROME WITH MILD MITOCHONDRIAL COMPLEX III DEFICIENCY
  GRACILE SYNDROME
  GRACILE SYNDROME (GRACILE)
  LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX III DEFICIENCY
  MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR 1 (MC3DN1)
  MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1
  MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1,
30
2
12
2
18
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:

BCS1_N - pfam08740
AAA - cd00009
AAA - smart00382
AAA - pfam00004


Swiss-Prot Protein: Q9Y276
Identical to: NP_004319, NP_001073335
   Default View:





Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
Q9Y276AAAcd000091963553.3e-09
Q9Y276AAApfam000042263556.2e-25
Q9Y276BCS1_Npfam08740231911.6e-79
Q9Y276AAAsmart003822223578.1e-11



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