Phenotypes associated with this allele

• Allele Symbol: Snx22^{tm1.1(KOMP)Wtsi}
• Allele Name: targeted mutation 1.1, Wellcome Trust Sanger Institute
• Allele ID: MGI:5605826
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Snx22^tm1.1(KOMP)Wtsi/Snx22^tm1.1(KOMP)Wtsi	C57BL/6N-Snx22^tm1.1(KOMP)Wtsi/Tcp	MGI:5757754

Genotype
MGI:5757754

hm1

• Allelic Composition: Snx22^{tm1.1(KOMP)Wtsi}/Snx22^{tm1.1(KOMP)Wtsi}
• Genetic Background: C57BL/6N-Snx22^{tm1.1(KOMP)Wtsi}/Tcp
• Cell Lines: EPD0416_4_C08

Data Sources

IMPC Data for Snx22

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

behavior/neurological

hyperactivity ( J:211773 )

♀

IMPC - UCD

mortality/aging

preweaning lethality, incomplete penetrance ( J:211773 )

♂

IMPC - UCD

reproductive system

abnormal uterus morphology ( J:211773 )

♀

IMPC - UCD