功能: disease:Defects in FAM20C are the cause of Raine syndrome (RNS) [MIM:259775]. RNS is an autosomal recessive osteosclerotic bone dysplasia with neonatal lethal outcome. Clinical features include generalized osteosclerosis, craniofacial dysplasia and microcephaly.,function:Calcium-binding protein which may play a role in dentin mineralization.,similarity:Belongs to the FAM20 family.,tissue specificity:Widely expressed.,
功能: disease:Defects in FAM20C are the cause of Raine syndrome (RNS) [MIM:259775]. RNS is an autosomal recessive osteosclerotic bone dysplasia with neonatal lethal outcome. Clinical features include generalized osteosclerosis, craniofacial dysplasia and microcephaly.,function:Calcium-binding protein which may play a role in dentin mineralization.,similarity:Belongs to the FAM20 family.,tissue specificity:Widely expressed.,
相關(guān)產(chǎn)品: RS0001,RS0002,YM3028,YM3029
細(xì)胞定位: Secreted . Golgi apparatus .
組織表達(dá): Widely expressed.
科研貨號: PLA020373
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