About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Nus1tm1.1Qrm
targeted mutation 1.1, Qing Robert Miao
MGI:5911854
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Nus1tm1.1Qrm/Nus1tm1.1Qrm
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: 129 * C57BL/6 * DBA * SJL MGI:6106900
cn2
Nr1h3tm1Djm/Nr1h3tm1Djm
Nus1tm1.1Qrm/Nus1tm1.1Qrm
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: 129 * C57BL/6 * DBA * SJL MGI:6106901
cn3
Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sortm1(cre/ERT2)Tyj
Nus1tm1.1Qrm/Nus1tm1.1Qrm
involves: 129 * C57BL/6 * SJL MGI:6106902
cn4
Nus1tm1.1Qrm/Nus1tm1.1Qrm
Tg(Cdh5-cre/ERT2)1Rha/0
involves: 129P2/OlaHsd * C57BL/6 MGI:6361030
cn5
Nus1tm1.1Qrm/Nus1tm1.1Qrm
Tg(Tek-cre)1Ywa/0
involves: 129P2/OlaHsd * C57BL/6 * SJL MGI:6361029


Genotype
MGI:6106900
cn1
Allelic
Composition
Nus1tm1.1Qrm/Nus1tm1.1Qrm
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
Genetic
Background
involves: 129 * C57BL/6 * DBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nus1tm1.1Qrm mutation (0 available); any Nus1 mutation (19 available)
Speer6-ps1Tg(Alb-cre)21Mgn mutation (6 available); any Speer6-ps1 mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• induction of hepatic lipogenesis when fed Western diet
• both total and free when fed Western diet
• both total and free when fed Western diet
• when fed Western diet
• when fed Western diet

liver/biliary system
• both total and free when fed Western diet
• when fed Western diet
• when fed Western diet




Genotype
MGI:6106901
cn2
Allelic
Composition
Nr1h3tm1Djm/Nr1h3tm1Djm
Nus1tm1.1Qrm/Nus1tm1.1Qrm
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
Genetic
Background
involves: 129 * C57BL/6 * DBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nr1h3tm1Djm mutation (3 available); any Nr1h3 mutation (32 available)
Nus1tm1.1Qrm mutation (0 available); any Nus1 mutation (19 available)
Speer6-ps1Tg(Alb-cre)21Mgn mutation (6 available); any Speer6-ps1 mutation (4 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
N
• when fed Western diet
• circulating triglyceride level
• liver triglyceride level
• circulating free fatty acid level
• liver free fatty acid level
• circulating cholesterol level both total and free
• both total and free when fed Western diet

liver/biliary system
• both total and free when fed Western diet




Genotype
MGI:6106902
cn3
Allelic
Composition
Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sortm1(cre/ERT2)Tyj
Nus1tm1.1Qrm/Nus1tm1.1Qrm
Genetic
Background
involves: 129 * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gt(ROSA)26Sortm1(cre/ERT2)Tyj mutation (3 available); any Gt(ROSA)26Sor mutation (944 available)
Nus1tm1.1Qrm mutation (0 available); any Nus1 mutation (19 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• induction of hepatic lipogenesis when fed Western diet
• when fed Western diet
• when fed Western diet

liver/biliary system
• when fed Western diet
• when fed Western diet
• when fed Western diet




Genotype
MGI:6361030
cn4
Allelic
Composition
Nus1tm1.1Qrm/Nus1tm1.1Qrm
Tg(Cdh5-cre/ERT2)1Rha/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nus1tm1.1Qrm mutation (0 available); any Nus1 mutation (19 available)
Tg(Cdh5-cre/ERT2)1Rha mutation (3 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• E10.5 embryos from tamoxifen-treated mothers exhibit aberrant cerebral blood vessel pattering
• E10.5 embryos from tamoxifen-treated mothers have dilated and disrupted organization of blood vessels

embryo
• E01.5 embryos are smaller in size when pregnant females are treated with tamoxifen at E8.5

growth/size/body
• E01.5 embryos are smaller in size when pregnant females are treated with tamoxifen at E8.5

nervous system
• E10.5 embryos from tamoxifen-treated mothers exhibit aberrant cerebral blood vessel pattering




Genotype
MGI:6361029
cn5
Allelic
Composition
Nus1tm1.1Qrm/Nus1tm1.1Qrm
Tg(Tek-cre)1Ywa/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Nus1tm1.1Qrm mutation (0 available); any Nus1 mutation (19 available)
Tg(Tek-cre)1Ywa mutation (6 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

growth/size/body

embryo
• E10, but not E9, yolk sac shows aberrant blood vessel development

cardiovascular system
• cerebral blood vessels are truncated and exhibit disrupted organization instead of having a well-organized tree-like pattern
• cerebral blood vessels are highly dilated, being normal at E8.5 but becoming dilated by E9.5
• cerebral blood vessels are truncated and exhibit disrupted organization instead of having a well-organized tree-like pattern
• the communicating artery is lost and disruption of major artery patterning is seen
• E10, but not E9, yolk sac shows aberrant blood vessel development
• however, no defect in cardiac development is seen and no obvious bronchial arch artery defects are seen
• E10, but not E9, yolk sac shows aberrant blood vessel development

nervous system
• cerebral blood vessels are truncated and exhibit disrupted organization instead of having a well-organized tree-like pattern
• cerebral blood vessels are highly dilated, being normal at E8.5 but becoming dilated by E9.5





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
04/30/2024
MGI 6.23
The Jackson Laboratory