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Phenotypes Associated with This Genotype
Genotype
MGI:7311572
Allelic
Composition
Lmnatm1.1Otin/Lmnatm1.1Otin
Nat10tm1a(KOMP)Wtsi/Nat10+
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Lmnatm1.1Otin mutation (0 available); any Lmna mutation (76 available)
Nat10tm1a(KOMP)Wtsi mutation (2 available); any Nat10 mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• delayed compared to mice homozygous for the Lmnatm1.1Otin and wild-type Nat10

reproductive system
N
• unlike mice homozygous for the Lmnatm1.1Otin, mice do not exhibit penis prolapse
• partially rescued compared to mice homozygous for the Lmnatm1.1Otin and wild-type Nat10

skeleton
• delayed compared to mice homozygous for the Lmnatm1.1Otin and wild-type Nat10

vision/eye
N
• unlike mice homozygous for the Lmnatm1.1Otin, mice do not exhibit keratoconjunctivitis sicca

cardiovascular system
• delayed onset

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
progeria DOID:3911 OMIM:176670
J:261974


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)
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last database update
09/22/2022
MGI 6.21
The Jackson Laboratory