KRT86 Polyclonal Antibody, 50ul Enzymes Mutations in RAB3GAP1 are associated

Mutations in RAB3GAP1 are associated with Warburg micro syndrome

esophageal squamous cell carcinoma

A microdeletion in the region of chromosome 20 where this gene is located has been associated with pseudohypoparathyroidism type Ib

one of which was initially identified as a MYC-interacting protein with features of a tumor suppressor

hypofibrinogenemia

KRT86 Polyclonal Antibody, 50ul Enzymes Mutations in RAB3GAP1 are associatedThis gene encodes a type II keratin protein, which heterodimerizes with type I keratins to form hair and nails. This gene is present in a cluster of related genes and pseudogenes on chromosome 12. Mutations in this gene have been observed in patients with the hair disease monilethrix.