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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for DFNB31 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID25861
Official gene symbolDFNB31
Full namedeafness, autosomal recessive 31
Aliases,CIP98,DKFZp434N014,KIAA1526,RP11-9M16.1,USH2D,WHRN,WI,
Gene summaryThis gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.
LocationChromosome: 9   Locus: 9q32-q34
Gene position117267736 - 117164360  Map Viewer
Gene orientationminus
Gene size103377 bp
Gene sequence
OMIM ID607928