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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ucntm1Klee
targeted mutation 1, Kuo-Fen Lee
MGI:2384136
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ucntm1Klee/Ucntm1Klee involves: 129S4/SvJae * C57BL/6J MGI:3840554


Genotype
MGI:3840554
hm1
Allelic
Composition
Ucntm1Klee/Ucntm1Klee
Genetic
Background
involves: 129S4/SvJae * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ucntm1Klee mutation (0 available); any Ucn mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• in the elevated plus maze, mutant mice spend significantly less time in the open arms than do control littermates, and mutant mice also enter the open arms fewer times than do controls; overall activity in closed-arm entries and total arm entries is not different between the mutant and control mice
• however, in the light/dark emergence test, no detectable differences are seen between mutant and control mice; the mutant mice had as many transitions between the light and dark portions of the box as did wildtype controls
• in the open-field test, mutant mice show greater anxiety-like behavior, spending less time in the inner squares than controls

hearing/vestibular/ear
N
• in mutant mice, the organ of Corti appeared grossly normal
• no gross qualitative differences in the number of nerve terminals contacting the outer hair cells or present in the inner spiral bundle, or in the expression of CGRP and vesicular Ach transporter in the terminals in mutant mice compared with littermate controls at three months of age
• outer hair-cell length is smaller in mutant mice compared to controls (wild type, 13.8 angstroms, 0.6 microm; mutant mice, 12.4 angstroms, 0.3 microm; P < 0.05)
• at all frequencies, the mutant mice consistently showed a higher threshold for the stimuli than control littermates at both 3 and 6 months of age
• distortion-product otoacoustic emissions are higher in mutant mice at all ages tested; however, there is no significant change in the level of distortion products within a genotype pool in relation to age (3 vs. 6 months of age)

homeostasis/metabolism
N
• after acute restraint, stress hormone secretion profiles, including ACTH and corticosterone, of mutant mice do not differ from those of control littermates
• daily basal food intake of Ucn mutants of both sexes as well as food intake and body weight in response to 24 hours of food deprivation is similar in both mutant and control mice

nervous system
N
• cresyl violet (Nissl) staining of brain sections show no apparent cytoarchitectural abnormalities in mutant mice
• outer hair-cell length is smaller in mutant mice compared to controls (wild type, 13.8 angstroms, 0.6 microm; mutant mice, 12.4 angstroms, 0.3 microm; P < 0.05)





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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory