TEFF1 Polyclonal Antibody, 100ul Antibodies Mutations in FMN2 have been

Mutations in FMN2 have been associated with mental retardation autosomal recessive 47 (MRT47)

Defective blue vision is characteristic

protein homology

This protein is expressed in keratinocytes and the gene is found on chromosome 9| adjacent to the type I interferon cluster

TEFF1 Polyclonal Antibody, 100ul Antibodies Mutations in FMN2 have beenMay inhibit NODAL and BMP signaling during neural patterning (By similarity). May be a tumor suppressor in brain cancers.,Belongs to the tomoregulin family.,Belongs to the UPF0439 family.,Contains 1 EGF like domain.,Contains 2 Kazal like domains.,subunit: May interact with ST14.,tissue specificity: Expressed in brain.,tissue specificity: Expressed predominantly in brain, and at lower levels in heart, placenta and skeletal muscle. Down regulated in