Link to the
Reference Paper. The accession number of this mRNA is
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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