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

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

5% of the human genome and encodes over 1

This gene is part of a functionally diverse eight-member protein subfamily of the PMP-22/EMP/MP20 family and is located in a cluster with two family members

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

This gene is expressed predominantly in T-cells

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