About Help FAQ

Symbol
Name
ID

Lmna
lamin A
MGI:96794

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Shallow orbits	Corneal ulceration	Corneal opacity	Cataract	Abnormality of retinal pigmentation	Retinal degeneration	Proptosis	Ptosis
Disease(s) Associated with LMNA	Shallow orbits	Corneal ulceration	Corneal opacity	Cataract	Abnormality of retinal pigmentation	Retinal degeneration	Proptosis	Ptosis
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
Emery-Dreifuss muscular dystrophy
mandibuloacral dysplasia type A lipodystrophy
progeria
restrictive dermopathy 2
Werner syndrome

Mouse Phenotypes		shallow orbits	keratoconjunctivitis sicca	abnormal optic disk morphology	abnormal cornea morphology	cornea ulcer	exophthalmos	ocular hypotelorism
Availability	Mouse Genotype	shallow orbits	keratoconjunctivitis sicca	abnormal optic disk morphology	abnormal cornea morphology	cornea ulcer	exophthalmos	ocular hypotelorism
	Lmna^tm1.1Otin/Lmna^tm1.1Otin
	Lmna^Dhe/Lmna⁺
	Lmna^{tm1b(EUCOMM)Wtsi}/Lmna⁺

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 05/14/2024 MGI 6.23