Phenotypes associated with this allele

• Allele Symbol: Aptx^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5634963
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Aptx^tm1b(EUCOMM)Hmgu/Aptx^tm1b(EUCOMM)Hmgu	B6N(Cg)-Aptx^tm1b(EUCOMM)Hmgu/J	MGI:6261888

Genotype
MGI:6261888

hm1

• Allelic Composition: Aptx^{tm1b(EUCOMM)Hmgu}/Aptx^{tm1b(EUCOMM)Hmgu}
• Genetic Background: B6N(Cg)-Aptx^{tm1b(EUCOMM)Hmgu}/J
• Cell Lines: HEPD0720_1_C02

Data Sources

IMPC Data for Aptx

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

homeostasis/metabolism

increased circulating alanine transaminase level ( J:211773 )

♂

IMPC - JAX

skeleton

decreased bone mineral content ( J:211773 )

♂

IMPC - JAX

decreased bone mineral density ( J:211773 )

♀

IMPC - JAX

vision/eye

cataract ( J:211773 )

♀

IMPC - JAX

persistence of hyaloid vascular system ( J:211773 )

IMPC - JAX