STRAIN INFORMATION


Family Identifier
NMF12
Synonym(s)
C57BL/6J-nmf12/J; JR#4110
Synopsis
Thin retina; white intraretinal patches.
Gene Symbol
nmf12 (View MGI Record)
Gene
neuroscience mutagenesis facility12
Allele Symbol
nmf12 (View MGI Record)
Allele
neuroscience mutagenesis facility12
Abnormal Assay(s)
Assay: Indirect ophthalmoscopy

   Domain(s): Eye/Vision

Assay: Eye histology

   Domain(s): Eye/Vision
Phenotype Description
Single mutant found at 13 weeks of age with retinal patch in left eye. The original mutant was non-productive and ovarian transplants of mutant ovaries also produced no offspring. However, matings of presumed heterozygotes have produced additional offspring.
Pathology Report
Standard pathology work-up on 3 mutants (266, 325 or 360 days of age) showed thinning of the peripheral retinae in both eyes. One eye also showed a small area in which the outer nuclear layer was very thin.
HERITABILITY AND MAPPING INFORMATION
Background Strain
C57BL/6J
Heritability Mode
Recessive
Heritability Status
Proven; 7 heterozygote matings produced 31 affected mice in a total of 142 progeny.
STATUS INFORMATION
Mutant Status
Cryopreserved Embryos
Comments
Please note: 1-The majority of frozen NMF embryos is obtained through matings between homozygous (or heterozygous) mutant males and wild-type females; if recovery of mutants is requested, the mice will be shipped as soon as possible following wean without further phenotype or genotype testing. NMF embryos are supplied subject to the General Terms and Conditions of Sale posted at www.jaxmice.jax.org. For prices or further information, please inquire at srp@jax.org or nmf-mice@jax.org; 2-This mutation has not yet been chromosomally mapped - an important part of determining whether it is allelic with a previously characterized mutation. (89) NMF12 have been requested by and distributed to 2 investigators.
Contact e-Mail Address
nmf-mice@jax.org