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Phenotypes Associated with This Genotype
Genotype
MGI:8345880
Allelic
Composition
Pahem1Coha/Pahem1Coha
Genetic
Background
C57BL/6NJ-Pahem1Coha
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pahem1Coha mutation (0 available); any Pah mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice struggle to wean from nursing to solid food, with increased mortality at weaning

pigmentation
• mice that survive beyond weaning exhibit coat color hypopigmentation on an unrestricted diet

behavior/neurological
• mice struggle to wean from nursing to solid food

homeostasis/metabolism
• serum tyrosine levels are lower in 6-12-week-old mice
• brain phenylalanine content is elevated
• however, no differences in brain tyrosine or tryptophan content
• mice treated with liver tropic recombinant adeno-associated virus serotype 8 containing murine Pah cDNA gene-therapy exhibit substantial correction of phenylalanine levels in the brain 14 days post-administration
• serum phenylalanine levels are elevated in 6-12-week-old mice
• mice treated with liver tropic recombinant adeno-associated virus serotype 8 containing murine Pah cDNA gene-therapy exhibit substantial correction of phenylalanine levels in the blood 14 days post-administration
• brain serotonin and 5-HIAA content is decreased
• however, brain dopamine levels are normal
• PAH enzymatic activity is undetectable in the liver
• mice treated with murine Pah gene-therapy exhibit liver PAH enzyme activity

integument
• mice that survive beyond weaning exhibit coat color hypopigmentation on an unrestricted diet

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
phenylketonuria DOID:9281 OMIM:261600
J:380540


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)
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last database update
05/26/2026
MGI 6.24
The Jackson Laboratory