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Results for Proteins associated with the Gene: KCTD7
KCTD7
154881


Known Diseases associated with this Protein:
  EPILEPSY, PROGRESSIVE MYOCLONIC 3, WITH INTRACELLULAR INCLUSIONS
  EPILEPSY, PROGRESSIVE MYOCLONIC 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS (EPM3)
  EPILEPSY, PROGRESSIVE MYOCLONIC 3, WITHOUT INTRACELLULAR INCLUSIONS
16
2
12
0
6
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:

BTB - smart00225
K_tetra - pfam02214


Swiss-Prot Protein: Q96MP8
Identical to: NP_694578
   Default View:



Default View:

BTB - smart00225
K_tetra - pfam02214



Default View:

BTB - smart00225
K_tetra - pfam02214


RefSeq Protein: NP_694578
   Default View:




Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕
Q96MP8K_tetrapfam02214531412.5e-23
Q96MP8BTBsmart00225481422.2e-11
NP_001161433K_tetrapfam02214531412.5e-23
NP_001161433BTBsmart00225481422.2e-11
NP_694578K_tetrapfam02214531412.5e-23
NP_694578BTBsmart00225481422.2e-11



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