Protein Überblick

The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance.

Alternative names and synonyms associated with ROR2

• receptor tyrosine kinase like orphan receptor 2 (ROR2) Antikörper
• receptor tyrosine kinase-like orphan receptor 2 (Ror2) Antikörper
• receptor tyrosine kinase like orphan receptor 2 (ror2) Antikörper
• receptor tyrosine kinase like orphan receptor 2 (Ror2) Antikörper
• receptor tyrosine kinase like orphan receptor 2 L homeolog (ror2.L) Antikörper

• bdb Antikörper
• bdb1 Antikörper
• LOC100219935 Antikörper
• MGC97773 Antikörper
• mRor2 Antikörper
• Alle Synonyme
• ntrkr2 Antikörper
• ror2 Antikörper
• xror2 Antikörper

Bezeichner auf Proteinebene für ROR2

neurotrophic tyrosine kinase receptor-related 2 , tyrosine-protein kinase transmembrane receptor ROR2 , neurotrophic tyrosine kinase, receptor related 2 , neurotrophic tyrosine kinase, receptor-related 2 , receptor tyrosine kinase-like orphan receptor 2 , tyrosine-protein kinase transmembrane receptor ROR2-like , LOW QUALITY PROTEIN: tyrosine-protein kinase transmembrane receptor ROR2 , receptor tyrosine kinase Xror2 , receptor tyrosine kinase like orphan receptor 2 L homeolog , receptor tyrosine kinase-like orphan receptor 2 L homeolog