Home News About DMDM Database Statistics Research Publications Contact  

 
  Domain Name: CypX
Cytochrome P450 [Secondary metabolites biosynthesis, transport, and catabolism]
No pairwise interactions found for the domain CypX

Total Mutations Found: 369
Total Disease Mutations Found: 116
This domain occurred 56 times on human genes (97 proteins).



  17,20-@LYASE DEFICIENCY, ISOLATED
  17-@ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY, COMBINED COMPLETE
  17-@ALPHA-HYDROXYLASE/17,20-LYASE DEFICIENCY, COMBINED PARTIAL
  ADENOMA, CORTISOL-PRODUCING, INCLUD
  ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
  ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY,
  ADRENAL HYPERPLASIA, CONGENITAL, DUE TO STEROID 11-BETA-HYDROXYLASE
  ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL
  AROMATASE DEFICIENCY
  BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY
  BILE ACID SYNTHESIS DEFECT, CONGENITAL, 3
  BREAST CANCER, SUSCEPTIBILITY TO, INCLUDED
  CEREBROTENDINOUS XANTHOMATOSIS
  CLASSIC TYPE
  CYP2A6*11
  DEBRISOQUINE, POOR METABOLISM OF
  DEBRISOQUINE, ULTRARAPID METABOLISM OF
  DEFICIENCY
  EFAVIRENZ CENTRAL NERVOUS SYSTEM TOXICITY, SUSCEPTIBILITY TO, INCLUDED
  EFAVIRENZ, POOR METABOLISM OF
  GHOSAL HEMATODIAPHYSEAL SYNDROME
  GLIPIZIDE POOR M
  HYPERCALCEMIA, INFANTILE
  ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5
  MEPHENYTOIN, POOR METABOLISM OF
  NONCLASSIC TYPE
  OR COMPLETE
  PHENYTOIN POOR METABOLIZER, INCLUDED;;
  PROGUANIL, POOR METABOLISM OF, INCLUDED
  RADIOHUMERAL FUSIONS WITH OTHER SKELETAL AND CRANIOFACIAL ANOMALIES
  SALT-WASTING TYPE
  SPASTIC PARAPLEGIA 56, AUTOSOMAL RECESSIVE
  SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE
  SPASTIC PARAPLEGIA 5A, AUTOSOMAL RECESSIVE, INCLUDED
  TEGAFUR, POOR METABOLISM OF
  TOLBUTAMIDE POOR METABOLIZER
  VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1A
  VITAMIN D HYDROXYLATION-DEFICIENT RICKETS, TYPE 1B
  WARFARIN SENSITIVITY
  WARFARIN SENSITIVITY, INCLUDED;;


Tips:
 If you've navigated here from a protein, hovering over a position on the weblogo will display the corresponding protein position for that domain position.

 The histograms below the weblogo indicate mutations found on the domain. Red is for disease (OMIM) and blue is for SNPs.

 Functional Features are displayed as orange boxes under the histograms. You can choose which features are displayed in the box below.



Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for CypX



















Weblogos are Copyright (c) 2002 Regents of the University of California




Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

   |   1000 Hilltop Circle, Baltimore, MD 21250   |   Department of Biological Sciences   |   Phone: 410-455-2258