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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cep78em2Gpt
endonuclease-mediated mutation 2, GemPharmatech Co., Ltd
MGI:7296812
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cep78em2Gpt/Cep78em2Gpt C57BL/6JGpt-Cep78em2Gpt MGI:7444965


Genotype
MGI:7444965
hm1
Allelic
Composition
Cep78em2Gpt/Cep78em2Gpt
Genetic
Background
C57BL/6JGpt-Cep78em2Gpt
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cep78em2Gpt mutation (0 available); any Cep78 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• abnormal or absent
• with disorganized microtubule doublets and missing central pairs
• in some sperm
• infertility could not be overcome with intracytoplasmic sperm injection
• fertilization phenotype could not be overcome with intracytoplasmic sperm injection

vision/eye
• in 6-month-old mice
• in 6-month-old mice
• grayish retinal pigment mottling at 3 months of age resembling retinitis pigmentosa
• in dark adapted mice at 6 months of age
• reduced following light adaptation at 3 and 6 months of age
• slightly in dark adapted mice at 3 and 6 months of age

hearing/vestibular/ear
• moderate to severe sensorineural hearing loss at 3 months of age with increased hearing loss at 6 months of age

nervous system
• in 6-month-old mice
• in 6-month-old mice

cellular
• abnormal or absent
• with disorganized microtubule doublets and missing central pairs
• in some sperm





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory