Mouse Kallikrein 6, KLK6 ELISA Kit , 96T Bio-Reaction Tube Defects in this gene have

Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17| Epstein syndrome| Alport syndrome with macrothrombocytopenia| Sebastian syndrome| Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness

These structures were shown to consist of cell-to-cell channels that facilitate the transfer of ions and small molecules between cells

Polymorphisms in this gene have been implicated in modifying risk of Parkinson disease

This olfactory receptor gene is a segregating pseudogene

Mouse Kallikrein 6, KLK6 ELISA Kit , 96T Bio-Reaction Tube Defects in this gene haveGlandular kallikreins cleave Met Lys and Arg Ser bonds in kininogen to release Lys bradykinin.