Phenotypes associated with this allele

• Allele Symbol: P3h1^{tm1b(EUCOMM)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5708192
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	P3h1^tm1b(EUCOMM)Wtsi/P3h1^tm1b(EUCOMM)Wtsi	C57BL/6N-P3h1^tm1b(EUCOMM)Wtsi/Ucd	MGI:5797692

Genotype
MGI:5797692

hm1

• Allelic Composition: P3h1^{tm1b(EUCOMM)Wtsi}/P3h1^{tm1b(EUCOMM)Wtsi}
• Genetic Background: C57BL/6N-P3h1^{tm1b(EUCOMM)Wtsi}/Ucd
• Cell Lines: EPD0821_6_C11

Data Sources

IMPC Data for P3h1

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

adipose tissue

increased total body fat amount ( J:211773 )

♀

IMPC - UCD

behavior/neurological

decreased grip strength ( J:211773 )

IMPC - UCD

decreased locomotor activity ( J:211773 )

IMPC - UCD

cardiovascular system

abnormal heart morphology ( J:211773 )

♂

IMPC - UCD

enlarged heart ( J:211773 )

♂

IMPC - UCD

prolonged RR interval ( J:211773 )

♀

IMPC - UCD

growth/size/body

enlarged heart ( J:211773 )

♂

IMPC - UCD

decreased body length ( J:211773 )

♀

IMPC - UCD

integument

abnormal skin morphology ( J:211773 )

IMPC - UCD

thin skin ( J:211773 )

IMPC - UCD

limbs/digits/tail

abnormal limb position ( J:211773 )

♂

IMPC - UCD

muscle

abnormal skeletal muscle morphology ( J:211773 )

♂

IMPC - UCD

skeleton

decreased bone mineral content ( J:211773 )

IMPC - UCD

decreased bone mineral density ( J:211773 )

IMPC - UCD