receptor tyrosine kinase like orphan receptor 2(English)

• 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
• SCARF2, SKIL, SVEP1, TGF-β, THBS2, TIE2, VPO1, ANGPT2, ARB, CDH3, CETN2, EFEMP1, FCN3, FSTL3, FXR/RXR, GHR, HFpEF, HS3ST5, IGFBP-2, KERA, LMAN2, LPS, LRRK2, LTBP4, LXR/RXR, MAdCAM-1, NOTUM, NP, NT-proBNP, PKG1, PTPN1, PXDN, RSPO1
• Skeleton and bone (formation), Genetics
• https://www.ncb…h.gov/gene/4920
• https://doi.org…LURE.123.011146