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GTR Home > Conditions/Phenotypes > Deafness, autosomal recessive 26, modifier of

Deafness, autosomal recessive 26, modifier of

Synonyms
DFNM1; Deafness, nonsyndromic, modifier 1

Summary

DFNB26M is characterized by normal hearing despite the presence of homozygosity for a causative deafness mutation in the GAB1 gene (Yousaf et al., 2018). [from OMIM]

Genes See tests for all associated and related genes

  • Also known as: 5630401D24Rik, CGI-01, DFNB26, DFNB26M, DFNM1, EEF1AKNMT, KIAA0859, feat, METTL13
    Summary: methyltransferase 13, eEF1A N-terminus and K55

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