Symbol Name ID |
Lmna
lamin A MGI:96794 |
Darker colors indicate more annotations |
Human Phenotypes | Conductive hearing impairment |
Prominent ear helix |
Microtia |
High-frequency sensorineural hearing impairment |
Low-frequency sensorineural hearing impairment |
Hearing impairment |
Disease(s) Associated with LMNA | ||||||
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | ||||||
mandibuloacral dysplasia type A lipodystrophy | ||||||
progeria |
Mouse Phenotypes | increased middle ear goblet cell number |
prominent ears |
short ears |
abnormal ear morphology |
abnormal auditory bulla morphology |
abnormal ear development |
abnormal middle ear morphology |
abnormal auditory tube morphology |
abnormal middle ear epithelium morphology |
abnormal tympanic membrane morphology |
tympanic membrane retraction |
abnormal ear physiology |
increased or absent threshold for auditory brainstem response |
abnormal distortion product otoacoustic emission |
impaired hearing |
increased susceptibility to otitis media |
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Availability | Mouse Genotype | ||||||||||||||||
Lmnatm2Stw/Lmnatm2Stw | |||||||||||||||||
LmnaDhe/Lmna+ |
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 04/16/2024 MGI 6.23 |
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