Link to the Reference Paper. The accession number of this mRNA is M97639 .
The following files contain the results of information analyses of mutations confirmed or predicted to result in mRNA splicing mutations in ROR2.
These include potential cryptic splice sites.

Donor: sites found that alter the information content of donorsites

Acceptor: sites found that alter the information content of acceptor sites

Unparsable Inconsistencies between the described mutation and the human genome reference sequence, "presently not posted"

Total: sites found that alter the information ocontent of both acceptor and donor sites are listed according to the mutation

Original: : Original Mutation Table

 References:

 HUMAN MUTATION 22:1^11 (2003)

 MUTATION UPDATE

 One Gene, Two Phenotypes: ROR2Mutations in Autosomal Recessive Robinow Syndrome and Autosomal Dominant Brachydactyly Type B

 Ali R. Afzal* and Steve Jeffery

 Medical Genetics Unit, St George~Rs Hospital Medical School, London, UK

 

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