About   Help   FAQ
Tph2tm1Bdr
Targeted Allele Detail
Summary
Symbol: Tph2tm1Bdr
Name: tryptophan hydroxylase 2; targeted mutation 1, Michael Bader
MGI ID: MGI:3849838
Gene: Tph2  Location: Chr10:114914546-115020927 bp, - strand  Genetic Position: Chr10, 63.51 cM
Alliance: Tph2tm1Bdr page
Growth retardation and postnatal lethality in Tph2tm1Bdr/Tph2tm1Bdr mice

Show the 1 phenotype image(s) involving this allele.

Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:150042
Parent Cell Line:  E14TG2a (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsThe coding region of exon 1 and exon 2 were replaced with a neo cassette. The absence of transcripts coding for exons 1 through 6 was confirmed by western blot analysis on brain extracts. (J:150042)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 4 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Tph2 Mutation:  41 strains or lines available
References
Original:  J:150042 Alenina N, et al., Growth retardation and altered autonomic control in mice lacking brain serotonin. Proc Natl Acad Sci U S A. 2009 Jun 23;106(25):10332-7
All:  9 reference(s)

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
04/16/2024
MGI 6.23
The Jackson Laboratory