About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ntsr1tm1Fer
targeted mutation 1, Pascual Ferrara
MGI:2389321
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ntsr1tm1Fer/Ntsr1tm1Fer C57BL/6-Ntsr1tm1Fer MGI:3041452
hm2
Ntsr1tm1Fer/Ntsr1tm1Fer Not Specified MGI:3044965


Genotype
MGI:3041452
hm1
Allelic
Composition
Ntsr1tm1Fer/Ntsr1tm1Fer
Genetic
Background
C57BL/6-Ntsr1tm1Fer
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntsr1tm1Fer mutation (0 available); any Ntsr1 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
adipose tissue
• at 20 weeks, increased body weight was correlated with a 2-fold increase in the epididymal and lumbar fat pad deposition; however, no differences were detected in the amount of brown adipose tissue fat pad or in blood glucose levels

behavior/neurological
N
• intracerebroventricular (i.c.v.) injection of neurotensin induced a similar analgesic effect on PBQ-induced writhing in homozygous null and wild-type mice
• homozygous null mice displayed no significant differences in spontaneous locomotion relative to wild-type; however, in contrast to control littermates, mutant mice failed to respond to neurotensin-induced (400 ng, via i.c.v.) hypolocomotion
• at 11 weeks, increased body weight in homozygous null males was correlated with a 10% increase in spontaneous food consumption relative to wild-type males; however, no significant differences were observed in water uptake, leptin, blood glucose, plasma insulin levels or in adipose tissue composition
• no differences were observed between wild-type and homozygous null mice in feeding behavior following 18 hours of food deprivation
• in wild-type mice, i.c.v. administration of 10 ng of neurotensin fully inhibited feeding for an hour, with a slow recovery in appetite; in contrast, neurotensin had no effect on the feeding behavior of mutant mice at either low or high neurotensin concentration
• i.c.v. administration of the orexigenic neuropeptide Y stimulated a similar increase in food consumption in wild-type and mutant male mice; also, the pattern of PYY binding was identical in both strains

growth/size/body
• both male and female homozygous null mice were viable, fertile, and displayed no obvious physical abnormalities
• starting at 10 weeks of age, homozygous null males became significantly heavier than wild-type males: a difference of 15% was noted at approximately 15 weeks persisting up to 45 weeks
• at 8 weeks, homozygous null females also displayed a small difference in body weight relative to wild-type; this difference persisted up to at least 12 weeks

homeostasis/metabolism
• untreated 11-week-old homozygous null mice were hyperthermic compared with wild-type littermates
• notably, i.c.v. administration of 200 ng of neurotensin to wild-type mice caused a drop in rectal temperature of 3.2 C; in contrast, i.c.v. injection of up to 400 ng neurotensin in homozygous null mice had no significant effect on rectal temperature




Genotype
MGI:3044965
hm2
Allelic
Composition
Ntsr1tm1Fer/Ntsr1tm1Fer
Genetic
Background
Not Specified
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ntsr1tm1Fer mutation (0 available); any Ntsr1 mutation (31 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
homeostasis/metabolism
• increases in extracellular dopamine induced by neurotensin injection into the ventral tegmental area of the brain are reduced compared to wild-type littermates





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
05/14/2024
MGI 6.23
The Jackson Laboratory