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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nat10tm1a(KOMP)Wtsi
targeted mutation 1a, Wellcome Trust Sanger Institute
MGI:5050156
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Nat10tm1a(KOMP)Wtsi/Nat10tm1a(KOMP)Wtsi C57BL/6NTac-Nat10tm1a(KOMP)Wtsi MGI:7311566
ht2
Nat10tm1a(KOMP)Wtsi/Nat10+ C57BL/6NTac-Nat10tm1a(KOMP)Wtsi MGI:7311568
cx3
Lmnatm1.1Otin/Lmnatm1.1Otin
Nat10tm1a(KOMP)Wtsi/Nat10+
involves: 129P2/OlaHsd * C57BL/6NTac MGI:7311572
cx4
Lmnatm1.1Otin/Lmna+
Nat10tm1a(KOMP)Wtsi/Nat10+
involves: 129P2/OlaHsd * C57BL/6NTac MGI:7311574


Genotype
MGI:7311566
hm1
Allelic
Composition
Nat10tm1a(KOMP)Wtsi/Nat10tm1a(KOMP)Wtsi
Genetic
Background
C57BL/6NTac-Nat10tm1a(KOMP)Wtsi
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nat10tm1a(KOMP)Wtsi mutation (2 available); any Nat10 mutation (70 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging




Genotype
MGI:7311568
ht2
Allelic
Composition
Nat10tm1a(KOMP)Wtsi/Nat10+
Genetic
Background
C57BL/6NTac-Nat10tm1a(KOMP)Wtsi
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nat10tm1a(KOMP)Wtsi mutation (2 available); any Nat10 mutation (70 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body




Genotype
MGI:7311572
cx3
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 (83 available)
Nat10tm1a(KOMP)Wtsi mutation (2 available); any Nat10 mutation (70 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




Genotype
MGI:7311574
cx4
Allelic
Composition
Lmnatm1.1Otin/Lmna+
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 (83 available)
Nat10tm1a(KOMP)Wtsi mutation (2 available); any Nat10 mutation (70 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• significantly delayed compared to in Lmnatm1.1Otin homozygotes

skeleton
• significantly delayed compared to in Lmnatm1.1Otin homozygotes

growth/size/body
• significantly delayed compared to in Lmnatm1.1Otin homozygotes

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





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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
09/03/2024
MGI 6.24
The Jackson Laboratory