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Results for Proteins associated with the Gene: COX7B
COX7B
1349


Known Diseases associated with this Protein:
  APLASIA CUTIS CONGENITA, RETICULOLINEAR, WITH MICROCEPHALY, FACIAL
  DYSMORPHISM, AND OTHER CONGENITAL ANOMALIES
1
0
1
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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:

COX7B - pfam05392
Cyt_c_Oxidase_VIIb - cd01403


Swiss-Prot Protein: P24311
Identical to: NP_001857
   Default View:




Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
P24311Cyt_c_Oxidase_VIIbcd0140329793.6e-41
P24311COX7Bpfam053921804.9e-65



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