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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Otop1tlt
tilted
MGI:1856638
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Otop1tlt/Otop1tlt B6.Cg-Otop1tlt/J MGI:3700197
hm2
Otop1tlt/Otop1tlt STOCK Oca2p-6H/Oca2p-d MGI:2182633


Genotype
MGI:3700197
hm1
Allelic
Composition
Otop1tlt/Otop1tlt
Genetic
Background
B6.Cg-Otop1tlt/J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Otop1tlt mutation (1 available); any Otop1 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• when dropped into a tank of water, most homozygous mice spiral immediately downward and require rescuing (J:49524)
• a small number of homozygotes could keep the nose but not the tail out of water; a few others could sometimes find the water surface but occasionally required rescuing (J:49524)
• observed in 50-75% of homozygous mice

hearing/vestibular/ear
N
• mice do not appear to have any hearing loss; ABR threshold determination shows similar levels compared to controls for all sound pressure levels tested
• histological analysis shows a grossly normal appearance of the middle ear and the bony and membranous labyrinths
• the sensory epithelia and otoconial membranes appear similar to controls; the otolithic membrane is visible over the surface of the maculae and there is no significant difference in the density of hair cells in the saccular and utricular maculae
• the cochlear duct, including the sensory and suppporting cells, cochlear nerve fibers and the tectorial membrane all appear similar to controls
• complete absence of otoconia from the saccule and the utricle is observed at 3-5 weeks of age as well as E17.5 and newborn homozygous mice (J:49524)
• in the rare mice that show a partial ability to swim, either otoconia are completely absent, or one or more giant otoconia are seen in the saccule (J:49524)
• absent vestibular nerve compund action potentials in response to linear acceleration at 9 and 16 pulses/s

nervous system
• morphometric analysis of the total vestibular ganglion volume and total cellular volume shows that mutants have reduced levels and developed slower than controls in the first 12 days of postnatal life




Genotype
MGI:2182633
hm2
Allelic
Composition
Otop1tlt/Otop1tlt
Genetic
Background
STOCK Oca2p-6H/Oca2p-d
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Otop1tlt mutation (1 available); any Otop1 mutation (38 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice cannot swim
• mice tuck the head towards the belly when picked up by the tail
• mice often hold head in tilted position





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory