Gene: [01p/CLCA2] chloride channel, calcium activated, 2;


KEY

 ion, trp, mem, sign

CLA

 coding, basic

LOC

 01 p31-22

MIM

 ?

Смотрите также:

  • Gene: [07q35/CLCN1] chloride channel 1, skeletal muscle; Thomsen's disease (myotonia congenita; autosomal dominant; MIM:160800); Becker's disease (generalized myotonia; autosomal recessive; MIM:255700);
  • Gene: [00.0/CLCA1] chloride channel, calcium activated, 1; [CaCC ]