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MUTANT LINE   NMF329 Contact JAX-NMF for ordering information
Synopsis:

The mutants are deaf.

Detailed Phenotype Description:

Routine examination for auditory function at 4-5 weeks of age revealed the mutants to be deaf. Acoustic startle response and Auditory brain stem recordings yielded no response at every frequency and intensity tested (click, 8, 16, 32 Hz at 30-90 dB). Mutants of either gender have been produced and the colony is maintained through homozygous breeding. Standard pathology work-up on two mutants (46 or 80 days of age) showed no abnormalities. Serial sections of the ears of the younger mutant showed some slight loss of hair cells in the left ear; whole-mount ear exam performed on the older mutant showed the presence of otoconia and no abnormalities.

Abnormal Assays:Domain(s):
Acoustic startle response (ASR) (view protocol) Auditory/Vestibular
Auditory brain stem response (ABR) (view protocol) Auditory/Vestibular


MUTANT LINE INFORMATION
Mutant Line Name
NMF329 (view more detail at Mutagenesis Center)
Gene Symbol nmf329 (view more info on gene)
Gene Name neuroscience mutagenesis facility329
Allele Symbol nmf329
Allele Name neuroscience mutagenesis facility329
MGI ID MGI:3055084 (view MGI record)
Originating Mutagenesis Center The Jackson Laboratory (contact for ordering information)
Mutation Type chemically induced mutation (CI)
Strain Designation C57BL/6J-nmf329/J


HERITABILITY AND MAPPING INFORMATION
Background Strain C57BL/6J
Mode of Inheritance Recessive
Heritability Proven
Chromosome Location 17
Mapping Interval D17Mit113 - 4.5 cM - (D17Mit197, nmf329) - 9.7 cM - D17Mit175; linkage: D17Mit197-LOD=9.67; D17Mit113-LOD=10.55
Identified Mutation
Map
(Click the image to zoom in.)
Image courtesy of MGI


STATUS INFORMATION
Availability
  • Cryopreserved embryos (EM)
Confirmation Date 09-Oct-2004
Availability Date 01-Nov-2004
Off-Shelf Date
Line History Comments (11) NMF329 have been requested by and distributed to 2 investigators.