Dfnb59 deafness, autosomal recessive 59 (human) (381375)

Symbol Product Feature Type Strand Chr
381375 Dfnb59 deafness, autosomal recessive 59 (human) protein-coding 2
Synonyms
Gm1001 | Pjvk
GO ID Category Definition Evidence
  • molecular_function
  • sensory perception of sound
  • neuronal cell body
Motif 1 Motif 2 Residual
Displaying 1 - 1 of 1
Entrez ID STRINGS Network
STRING
Log in or register to post comments