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Literature summary for 2.7.10.1 extracted from

  • Oldridge, M.; Fortuna, A.M.; Maringa, M.; Propping, P.; Mansour, S.; Pollitt, C.; DeChiara, T.M.; Kimble, R.B.; Valenzuela, D.M.; Yancopoulos, G.D.; Wilkie, A.O.
    Dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B (2000), Nat. Genet., 24, 275-278.
    View publication on PubMed

Protein Variants

Protein Variants Comment Organism
additional information dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Homo sapiens dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B ?
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?

Organism

Organism UniProt Comment Textmining
Homo sapiens Q01974
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-

Substrates and Products (Substrate)

Substrates Comment Substrates Organism Products Comment (Products) Rev. Reac.
additional information dominant mutations in ROR2, encoding an orphan receptor tyrosine kinase, cause brachydactyly type B Homo sapiens ?
-
?

Synonyms

Synonyms Comment Organism
tyrosine-protein kinase transmembrane receptor ROR2
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Homo sapiens