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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Htr2ctm1Knk
targeted mutation 1, Kazuko Nishikura
MGI:3823041
Summary 7 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Htr2ctm1Knk/Htr2ctm1Knk B6.Cg-Htr2ctm1Knk MGI:3823071
hm2
Htr2ctm1Knk/Htr2ctm1Knk C.Cg-Htr2ctm1Knk MGI:3823070
ht3
Htr2ctm1Knk/Htr2c+ B6.Cg-Htr2ctm1Knk MGI:3823076
ht4
Htr2ctm1Knk/Htr2ctm2Knk B6.Cg-Htr2ctm1Knk/Htr2ctm2Knk MGI:3823077
cx5
Htr2ctm1Knk/Y
Mc4rtm1Lowl/Mc4rtm1Lowl
involves: 129S4/SvJae * C57BL/6 MGI:3823073
ot6
Htr2ctm1Knk/Y B6.Cg-Htr2ctm1Knk MGI:3823072
ot7
Htr2ctm1Knk/Y C.Cg-Htr2ctm1Knk MGI:3823069


Genotype
MGI:3823071
hm1
Allelic
Composition
Htr2ctm1Knk/Htr2ctm1Knk
Genetic
Background
B6.Cg-Htr2ctm1Knk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Htr2ctm1Knk mutation (1 available); any Htr2c mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• less than 20% of mice survive the postnatal period
• however, removal of competing wild-type and female heterozygous littermates increases survival to 80%

growth/size/body
• despite normal birth weights, mice exhibit a 50% reduction in body weight gain compared to wild-type mice regardless of strain background or fostering with wild-type mothers
• however, between 3 and 5 weeks of age growth rates are normal
• mice exhibit decreased body length compared to wild-type mice but this difference becomes less significant after weaning




Genotype
MGI:3823070
hm2
Allelic
Composition
Htr2ctm1Knk/Htr2ctm1Knk
Genetic
Background
C.Cg-Htr2ctm1Knk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Htr2ctm1Knk mutation (1 available); any Htr2c mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• despite normal birth weights, mice exhibit a 50% reduction in body weight gain compared to wild-type mice regardless of strain background or fostering with wild-type mothers




Genotype
MGI:3823076
ht3
Allelic
Composition
Htr2ctm1Knk/Htr2c+
Genetic
Background
B6.Cg-Htr2ctm1Knk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Htr2ctm1Knk mutation (1 available); any Htr2c mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body




Genotype
MGI:3823077
ht4
Allelic
Composition
Htr2ctm1Knk/Htr2ctm2Knk
Genetic
Background
B6.Cg-Htr2ctm1Knk/Htr2ctm2Knk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Htr2ctm1Knk mutation (1 available); any Htr2c mutation (12 available)
Htr2ctm2Knk mutation (1 available); any Htr2c mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body




Genotype
MGI:3823073
cx5
Allelic
Composition
Htr2ctm1Knk/Y
Mc4rtm1Lowl/Mc4rtm1Lowl
Genetic
Background
involves: 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Htr2ctm1Knk mutation (1 available); any Htr2c mutation (12 available)
Mc4rtm1Lowl mutation (2 available); any Mc4r mutation (44 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice exhibit hyperphagia

growth/size/body
N
• unlike when either gene is knocked-out, mice exhibit normal growth rates
• at 6 weeks but not 16 weeks




Genotype
MGI:3823072
ot6
Allelic
Composition
Htr2ctm1Knk/Y
Genetic
Background
B6.Cg-Htr2ctm1Knk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Htr2ctm1Knk mutation (1 available); any Htr2c mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice exhibit convulsions and death at a dose of MK212 (a HTR2C-selective agonist) that is 100 times lower than in wild-type mice
• less than 20% of mice survive the postnatal period
• however, removal of competing wild-type and female heterozygous littermates increases survival to 80%

homeostasis/metabolism
N
• despite decreased growth, mice exhibit normal levels of thyroxine and corticosterone
• at 3 weeks but not 6 weeks
• at 3 weeks, circulating ghrelin levels are higher than in wild-type mice
• however, by 6 weeks circulating ghrelin levels are normal
• at 3 weeks, circulating leptin levels are lower than in wild-type mice
• however, leptin levels are normal at 6 weeks
• mice exhibit more prominent hypothermia than wild-type mice in response to 8-OH-DPAT (a HTR1A-specific agonist)
• however, untreated mice exhibit normal body temperature
• unlike in wild-type mice, metabolic rate is not increased by treatment with CL316243 (a beta-adrenergic-specific agonist)
• mice exhibit a 40% increase in basal metabolic rate compared to in wild-type mice
• treatment with SB242084 reduces energy expenditure but it remains higher than in wild-type mice
• mice exhibit convulsions and death at a dose of MK212 (a HTR2C-selective agonist) that is 100 times lower than in wild-type mice
• mice exhibit more prominent hypothermia than wild-type mice in response to 8-OH-DPAT (a HTR1A-specific agonist)
• mice exhibit convulsions and death at a dose of MK212 (a HTR2C-selective agonist) that is 100 times lower than in wild-type mice
• mice exhibit increased sensitivity to mCPP and Ro60-0174, HTR2C-selective agonists

growth/size/body
• adipose accumulation is lower than in wild-type mice
• mice exhibit decreased body length compared to wild-type mice but this difference becomes less significant after weaning
• postnatal growth retardation is not rescued by injection of growth hormone
• despite normal birth weights, mice exhibit a 50% reduction in body weight gain compared to wild-type mice regardless of strain background or fostering with wild-type mothers
• however, between 3 and 5 weeks of age growth rates are normal

behavior/neurological
• low doses of MK212 result in more pronounced hypoactivity than in wild-type mice, and food intake can be decreased by treatment with MK212 or mCPP
• low doses of SB242084, but not ketanserin or SB204741 (all HTR2C-specific antagonists) induce more hypolocomotion than in wild-type mice that cannot be reverted by treatment with haloperidol (a D2, D3 and D4 dopamine receptor antagonist) or R(+)-SCH23390 (a D1 dopamine receptor antagonist)
• mice exhibit hyperphagia
• however, food intake can be decreased by treatment with MK212
• mice are 2-fold less active than wild-type mice

adipose tissue
• adipose accumulation is lower than in wild-type mice




Genotype
MGI:3823069
ot7
Allelic
Composition
Htr2ctm1Knk/Y
Genetic
Background
C.Cg-Htr2ctm1Knk
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Htr2ctm1Knk mutation (1 available); any Htr2c mutation (12 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• despite normal birth weights, mice exhibit a 50% reduction in body weight gain compared to wild-type mice regardless of strain background or fostering with wild-type mothers





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory