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OTOF


Official Full Name
otoferlin
Organism
Homo sapiens
Gene ID
9381
Background
Mutations in this gene are a cause of neurosensory nonsyndromic recessive deafness, DFNB9. The short form of the encoded protein has 3 C2 domains, a single carboxy-terminal transmembrane domain found also in the C. elegans spermatogenesis factor FER-1 and human dysferlin, while the long form has 6 C2 domains. The homology suggests that this protein may be involved in vesicle membrane fusion. Several transcript variants encoding multiple isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Synonyms
AUNB1; DFNB6; DFNB9; NSRD9; FER1L2

Cat.No. Product Name Price
SHH368956 shRNA set against Human OTOF (NM_194248.2) Inquiry
SHH368960 shRNA set against Mouse OTOF (NM_031875.2) Inquiry
SHR082938 shRNA set against Mouse Otof(NM_031875.2) Inquiry
Cat.No. Product Name Price
CDFL009779 Mouse Otof cDNA Clone(NM_031875.2) Inquiry
MiUTR1M-08776 OTOF miRNA 3'UTR clone Inquiry
CDCB185526 Rabbit OTOF ORF clone (XM_008254653.1) Inquiry
CDCL145039 Mouse OTOF ORF clone (NM_194323.2) Inquiry
CDCL145045 Mouse Otof ORF clone (NM_001100395.1) Inquiry
CDCR263861 Mouse Otof ORF Clone(NM_031875.2) Inquiry
CDCR288881 Human OTOF ORF Clone(NM_004802.3) Inquiry
CDCR325284 Human OTOF ORF Clone(NM_194322.2) Inquiry
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