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DFNB59 / PJVK
deafness, autosomal recessive 59
DFNB59 / PJVK is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59).
| Gene Name: | deafness, autosomal recessive 59 |
| Synonyms: | DFNB59, Pejvakin, PJVK |
| Target Sequences: | NP_001036167.1 Q0ZLH3 |
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