About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Drd2-cre)ER44Gsat
transgene insertion ER44, GENSAT Project at Rockefeller University
MGI:3836635
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ehmt2tm1.1Tara/Ehmt2tm1.1Tara
Tg(Drd2-cre)ER44Gsat/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N MGI:4418569
cn2
Prkar2btm3Gsm/Prkar2btm2Gsm
Tg(Drd2-cre)ER44Gsat/0
involves: C57BL/6 * FVB/N MGI:5515337
cn3
Ppp1r1btm5.1Pggd/Ppp1r1btm5.1Pggd
Tg(Drd2-cre)ER44Gsat/0
Tg(Drd2-EGFP)S118Gsat/0
involves: C57BL/6 * FVB/N * FVB/NTac MGI:4830460


Genotype
MGI:4418569
cn1
Allelic
Composition
Ehmt2tm1.1Tara/Ehmt2tm1.1Tara
Tg(Drd2-cre)ER44Gsat/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ehmt2tm1.1Tara mutation (0 available); any Ehmt2 mutation (55 available)
Tg(Drd2-cre)ER44Gsat mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• small significant negative gain in excitability of medium spiny neurons

behavior/neurological
• greater increase in locomotor and exploratory behaviors in response to caffeine, a repressor of Drd2.
• greater increase in locomotor and exploratory behaviors in response by to caffeine, a repressor of Drd2




Genotype
MGI:5515337
cn2
Allelic
Composition
Prkar2btm3Gsm/Prkar2btm2Gsm
Tg(Drd2-cre)ER44Gsat/0
Genetic
Background
involves: C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkar2btm2Gsm mutation (1 available); any Prkar2b mutation (27 available)
Prkar2btm3Gsm mutation (0 available); any Prkar2b mutation (27 available)
Tg(Drd2-cre)ER44Gsat mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• hyperactivity phenotype is lost

adipose tissue

growth/size/body
• low body weight
• lean body

homeostasis/metabolism
• low serum leptin levels




Genotype
MGI:4830460
cn3
Allelic
Composition
Ppp1r1btm5.1Pggd/Ppp1r1btm5.1Pggd
Tg(Drd2-cre)ER44Gsat/0
Tg(Drd2-EGFP)S118Gsat/0
Genetic
Background
involves: C57BL/6 * FVB/N * FVB/NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ppp1r1btm5.1Pggd mutation (0 available); any Ppp1r1b mutation (18 available)
Tg(Drd2-cre)ER44Gsat mutation (2 available)
Tg(Drd2-EGFP)S118Gsat mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• loss of expression in striatopallidal and striatonigral neurons results in a reduced LTP at the corticostriatal synapses

behavior/neurological
• haloperidol-induced catalepsy is strongly reduced
• in an open-field test





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