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Literature summary for 2.7.10.1 extracted from

  • Van Bokhoven, H.; Celli, J.; Kayserili, H.; van Beusekom, E.; Balci, S.; Brussel, W.; Skovby, F.; Kerr, B.; Percin, E.F.; Akarsu, N.; Brunner, H.G.
    Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome (2000), Nat. Genet., 25, 423-426.
    View publication on PubMed
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Protein Variants

Protein Variants Comment Organism
additional information mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome Homo sapiens

Natural Substrates/ Products (Substrates)

Natural Substrates Organism Comment (Nat. Sub.) Natural Products Comment (Nat. Pro.) Rev. Reac.
additional information Homo sapiens mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome ?
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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 mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome Homo sapiens ?
-
 ?

Synonyms

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