No. of disease causing mutations: 1
| Identifier | Nucleotide change | Mutation | Amino acid change/ Predicted consequence | Location | Restriction site change | Reference |
|---|---|---|---|---|---|---|
| octsd.001 | c.G???>A | Missense | p.Asp269Asn
|
Tyynela et al. 2000 EMBO J 19:2786-2792 |
cDNA: AF164143
Genomic sequence:
The mutation at residue Asp269 of ovine CTSD corresponds to Asp295 of the human gene, and occurs at the equivalent nucleotide residue to G934 of the human CTSD cDNA
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