Phenotypes associated with this allele

• Allele Symbol: Prss2^{tm1.1(KOMP)Vlcg}
• Allele Name: targeted mutation 1.1, Velocigene
• Allele ID: MGI:5705866
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Prss2^tm1.1(KOMP)Vlcg/Prss2^tm1.1(KOMP)Vlcg	C57BL/6N-Prss2^tm1.1(KOMP)Vlcg/J	MGI:6263251

Genotype
MGI:6263251

hm1

• Allelic Composition: Prss2^{tm1.1(KOMP)Vlcg}/Prss2^{tm1.1(KOMP)Vlcg}
• Genetic Background: C57BL/6N-Prss2^{tm1.1(KOMP)Vlcg}/J
• Cell Lines: 11483A-F5

Data Sources

IMPC Data for Prss2

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

behavior/neurological

increased exploration in new environment ( J:211773 )

♂

IMPC - JAX

impaired righting response ( J:211773 )

IMPC - JAX

limb grasping ( J:211773 )

IMPC - JAX

decreased locomotor activity ( J:211773 )

♀

IMPC - JAX

homeostasis/metabolism

decreased circulating phosphate level ( J:211773 )

♀

IMPC - JAX

integument

abnormal coat/hair pigmentation ( J:211773 )

IMPC - JAX

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

IMPC - JAX

skeleton

decreased bone mineral content ( J:211773 )

♀

IMPC - JAX

decreased bone mineral density ( J:211773 )

♀

IMPC - JAX