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Results for Proteins associated with the Gene: FKTN
FKTN
2218


Known Diseases associated with this Protein:
  ANOMALIES), TYPE A, 4
  CARDIOMYOPATHY, DILATED 1X (CMD1X)
  CARDIOMYOPATHY, DILATED, 1X
  MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE
  MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITHOU
  MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (LIMB-GIRDLE), TYPE C, 4
  MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITH BRAIN AND EYE ANOMALIES A4 (MDDGA4)
  MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY CONGENITAL WITHOUT MENTAL RETARDATION B4 (MDDGB4)
  MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY LIMB-GIRDLE C4 (MDDGC4)
  RECLASSIFIED - VARIANT OF UNKNOWN SIGNIFICANCE
31
8
22
4
13
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:

LicD - pfam04991


Swiss-Prot Protein: O75072
Identical to: NP_006722, NP_001073270
   Default View:


Default View:

LicD - pfam04991



Default View:

LicD - pfam04991


RefSeq Protein: NP_006722
   Default View:


Default View:

LicD - pfam04991




Domains found on the Proteins

Protein ↕Domain ↕Domain Accession ↕Start ↕End ↕E-Value ↕



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