ROR2 is 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.

Long Name

Receptor Tyrosine Kinase-like Orphan Receptor 2

Alternate Names

BDB1, NTRKR2

Gene Symbol

ROR2

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Product Documents for ROR2 Antibody (ROR2/1912) [Janelia Fluor® 549]

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Product Specific Notices for ROR2 Antibody (ROR2/1912) [Janelia Fluor® 549]

Sold under license from the Howard Hughes Medical Institute, Janelia Research Campus.

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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ROR2 Antibody (ROR2/1912) [Janelia Fluor® 549]

Novus Biologicals, part of Bio-Techne | Catalog # NBP3-08784JF549

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Product Summary for ROR2 Antibody (ROR2/1912) [Janelia Fluor® 549]

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Applications for ROR2 Antibody (ROR2/1912) [Janelia Fluor® 549]

Immunohistochemistry-Paraffin

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Background: ROR2