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  Domain Name: ZnF_C2H2
zinc finger.
No pairwise interactions found for the domain ZnF_C2H2

Total Mutations Found: 249
Total Disease Mutations Found: 28
This domain occurred 723 times on human genes (1165 proteins).



  ANEMIA, DYSERYTHROPOIETIC CONGENITAL, TYPE IV
  BLOOD GROUP--LUTHERAN INHIBITOR
  BRITTLE CORNEA SYNDROME 2
  CARDIOMYOPATHY, DILATED, 1LL
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 1D
  CHARCOT-MARIE-TOOTH DISEASE, TYPE 1D, INCLUDED
  DEJERINE-SOTTAS NEUROPATHY, AUTOSOMAL DOMINANT
  DIABETES MELLITUS, TRANSIENT NEONATAL, 1
  DUANE-RADIAL RAY SYNDROME
  GREIG CEPHALOPOLYSYNDACTYLY SYNDROME
  HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, KLF1-RELATED
  HETEROTAXY, VISCERAL, 1, X-LINKED
  MENTAL RETARDATION, X-LINKED 97
  NEUROPATHY, CONGENITAL HYPOMYELINATING, AUTOSOMAL DOMINANT
  NEUTROPENIA, NONIMMUNE CHRONIC IDIOPATHIC, OF ADULTS
  NEUTROPENIA, SEVERE CONGENITAL, 2, AUTOSOMAL DOMINANT
  SKELETAL DEFECTS, GENITAL HYPOPLASIA, AND MENTAL RETARDATION
  VARIANT OF UNKNOWN SIGNIFICANCE


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for ZnF_C2H2





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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.

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