Symbol Name ID |
Lmna
lamin A MGI:96794 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Alopecia of scalp |
Sparse scalp hair |
Micrognathia |
Microretrognathia |
Retrognathia |
Malar flattening |
Hypoplastic facial bones |
Shallow orbits |
Relative macrocephaly |
Delayed cranial suture closure |
Wormian bones |
Large fontanelles |
Bird-like facies |
Craniofacial disproportion |
Round face |
Narrow face |
Full cheeks |
Midface retrusion |
Increased facial adipose tissue |
Short chin |
Thin vermilion border |
Ankyloglossia |
Short lingual frenulum |
High palate |
Narrow mouth |
Abnormality of the dentition |
Hypodontia |
Advanced eruption of teeth |
Delayed eruption of teeth |
Impacted tooth |
Persistence of primary teeth |
Hypoplasia of teeth |
Premature loss of teeth |
Dental crowding |
Neoplasm of the oral cavity |
Convex nasal ridge |
Narrow nasal ridge |
Abnormal nasal tip morphology |
Narrow nasal tip |
Wide nasal bridge |
Narrow nose |
Abnormal eyebrow morphology |
Absent eyebrow |
Loss of eyelashes |
Absent eyelashes |
Nocturnal lagophthalmos |
Disease(s) Associated with LMNA | ||||||||||||||||||||||||||||||||||||||||||||||
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome | ||||||||||||||||||||||||||||||||||||||||||||||
familial partial lipodystrophy type 2 | ||||||||||||||||||||||||||||||||||||||||||||||
mandibuloacral dysplasia type A lipodystrophy | ||||||||||||||||||||||||||||||||||||||||||||||
progeria | ||||||||||||||||||||||||||||||||||||||||||||||
restrictive dermopathy 2 | ||||||||||||||||||||||||||||||||||||||||||||||
Werner syndrome |
Mouse Phenotypes | craniofacial phenotype |
abnormal cranial suture morphology |
abnormal coronal suture morphology |
abnormal lambdoid suture morphology |
abnormal sagittal suture morphology |
wide cranial sutures |
abnormal frontonasal suture morphology |
abnormal cranium morphology |
abnormal cranium size |
decreased cranium height |
decreased cranium width |
small cranium |
abnormal neurocranium morphology |
abnormal zygomatic arch morphology |
shallow orbits |
abnormal incisor morphology |
small lower incisors |
short upper incisors |
malocclusion |
mandible hypoplasia |
short maxilla |
micrognathia |
abnormal hard palate morphology |
abnormal tongue morphology |
short snout |
prominent ears |
short ears |
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Availability | Mouse Genotype | |||||||||||||||||||||||||||
LmnaDhe/LmnaDhe | ||||||||||||||||||||||||||||
LmnaGt(S7-1F1)Sor/LmnaGt(S7-1F1)Sor | * | |||||||||||||||||||||||||||
Lmnatm1.1Otin/Lmnatm1.1Otin | ||||||||||||||||||||||||||||
Lmnatm1Lgf/Lmnatm1Lgf | ||||||||||||||||||||||||||||
Lmnatm2Stw/Lmnatm2Stw | ||||||||||||||||||||||||||||
LmnaDhe/Lmna+ | ||||||||||||||||||||||||||||
Lmnatm1Lgf/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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