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Literature summary for 2.7.10.1 extracted from

  • Afzal, A.R.; Rajab, A.; Fenske, C.D.; Oldridge, M.; Elanko, N.; Ternes-Pereira, E.; Tuysuz, B.; Murday, V.A.; Patton, M.A.; Wilkie, A.O.; Jeffery, S.
    Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2 (2000), Nat. Genet., 25, 419-422.
    View publication on PubMed
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Protein Variants

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

Localization Comment Organism GeneOntology No. Textmining
membrane
-
 Homo sapiens 16020
-

Natural Substrates/ Products (Substrates)

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

Organism UniProt Comment Textmining
Homo sapiens Q01974
-
-

Substrates and Products (Substrate)

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

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