Protein Variants | Comment | Organism |
---|---|---|
additional information | recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by loss of ROR2 activity. The identification of mutations in three distinct domains containing Frizzled-like, kringle and tyrosine kinase motifs indicates that these are all essential for ROR2 function | Homo sapiens |
Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|
membrane | - |
Homo sapiens | 16020 | - |
Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|
additional information | Homo sapiens | recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by loss of ROR2 activity | ? | - |
? |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | Q01974 | - |
- |
Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|
additional information | recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by loss of ROR2 activity | Homo sapiens | ? | - |
? |
Synonyms | Comment | Organism |
---|---|---|
tyrosine-protein kinase transmembrane receptor ROR2 | - |
Homo sapiens |