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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
NonoGt(YHA266)Byg
gene trap YHA266, BayGenomics
MGI:3866756
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ot1
NonoGt(YHA266)Byg/Y involves: 129P2/OlaHsd MGI:6469924
ot2
NonoGt(YHA266)Byg/Y involves: 129P2/OlaHsd * C57BL/6J MGI:5446136


Genotype
MGI:6469924
ot1
Allelic
Composition
NonoGt(YHA266)Byg/Y
Genetic
Background
involves: 129P2/OlaHsd
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
NonoGt(YHA266)Byg mutation (0 available); any Nono mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
N
• normal blood pressure
• normal ventricle size and non-compacted ventricular myocardium
• normal heart to body weight ratio
• normal left ventricular ejection fraction (LVEF), fractional shortening (FS) and left ventricular posterior wall thickness (LVPWd)
• at age 16 weeks
• at age 16 weeks
• increased extra-cellular matrix (ECM) with more collagen I and III
• decreased left ventricular end diastolic diameter (LVEDd)

mortality/aging
• significantly increased mortality rate up to age 1 year
• male mice born much below expected Mendelian ratio

growth/size/body
• at age 4 months; reduction larger in males than females

craniofacial

cellular
• increased extra-cellular matrix (ECM) with more collagen I and III
• reduced cardiac fibroblast migration
• increased cardiac fibroblast proliferation

homeostasis/metabolism
N
• normal fasting glucose, total cholesterol, triglyceride, LDL and HDL levels
• normal ventricle size and non-compacted ventricular myocardium
• normal heart to body weight ratio
• normal left ventricular ejection fraction (LVEF), fractional shortening (FS) and left ventricular posterior wall thickness (LVPWd)

liver/biliary system

behavior/neurological
N
• normal food intake

renal/urinary system
• right kidney




Genotype
MGI:5446136
ot2
Allelic
Composition
NonoGt(YHA266)Byg/Y
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
NonoGt(YHA266)Byg mutation (0 available); any Nono mutation (27 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• 2-fold increase of primary fibroblasts in S phase
• loss of circadian regulation of cell division in primary fibroblasts
• marked increased rate of population doubling of primary fibroblasts
• in primary fibroblasts

behavior/neurological
• decreased by 20 minutes compared to controls under constant dark conditions (J:189236)
• slight (J:193286)

liver/biliary system
• loss of circadian regulation of some genes in the liver

homeostasis/metabolism
• following a full-thickness incisional wound, immature granulation tissue is characterized by continued fibroblast proliferation, occupying most of the wound area
• collagen secretion is dramatically reduced
• dividing cells form only an immature dysfunctional epidermal layer resting on a disorganized granulation tissue that prevents healing





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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
05/07/2024
MGI 6.23
The Jackson Laboratory