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Allele : Tph1<tm1Bdr> tryptophan hydroxylase 1; targeted mutation 1, Michael Bader

Primary Identifier  MGI:2450301 Allele Type  Targeted
Attribute String  Null/knockout Gene  Tph1
Transmission  Germline Strain of Origin  Not Specified
Is Recombinase  false Is Wild Type  false
molecularNote  An isoform specific disruption of the endogenous allele was achieved by the insertion of neomycin and thymidine kinase cassettes via homologous recombination. The disruption putatively resulted in functional ablation in the peripheral tissues. The endogenous allele encodes the rate-limiting enzyme for serotonin synthesis, and while serotonin was detected at normal levels in the brain, it was absent in the periphery, with the exception of low levels (4% of wild-type) detected in the duodenum.
  • mutations:
  • Insertion
  • synonyms:
  • Tph<->,
  • Tph<->,
  • Tph1<->,
  • Tph1<->
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

39 Publication categories