Gene: PJVK ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 494513
Gene Symbol: PJVK
PJVK 		0.400 Biomarker phenotype CTD_human Previous studies have described two missense mutations in the human pejvakin gene that cause nonsyndromic recessive deafness (DFNB59) by affecting the function of auditory neurons. 17329413 2007
Entrez Id: 494513
Gene Symbol: PJVK
PJVK 		0.400 CausalMutation phenotype CLINVAR